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  • 1
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000) 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 17-29 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The dynamic behaviour of biofilters intended to remove toluene and xylene from air was studied during transient states. Laboratory scale biofilters were filled with a mixture of peat, bark and wood and inoculated with a mixed microbial population. Toluene and xylene were applied both as single pollutants and as mixtures. Attention was focused on the evaluation of the following transients: the response of biofilters to step changes and peaks in pollutant concentrations, the effect of changes between single and multiple pollutant loadings and the response to shutdown periods.The biofilters demonstrated a good dynamic stability during transient states induced by change in inlet pollutant concentrations. Their time periods did not exceed three hours. No interaction between xylene and toluene degradation was observed during changes in loading with single pollutants or their mixture. The performance interruptions lasting less than 24 hours were found to have no significant influence on the removal efficiency of biofilters. When the biofilters were reacclimated after longer starvation periods, a short temporary decrease in efficiency whose minimum and duration were proportional to the length of a preceding shutdown period was observed. The longest starvation period (7 days) resulted in a reacclimation lasting 7 hours only. Adaptations of a microbial population to new operating conditions as well as sorption/desorption processes were suggested as the main factors influencing the dynamic reponse characteristics.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 31-38 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: In this paper, the in vivo decolourization of the polymeric dye Poly R-478 by semi-solid-state cultures of Phanerochaete chrysosporium BKM-F-1767 (ATCC 24725) was investigated, employing corncob as a support. In order to stimulate the ligninolytic system of the fungus, the cultures were supplemented with veratryl alcohol (2 mM) or manganese (IV) oxide (1 g/l).Maximum manganese-dependent peroxidase (MnP) and lignin peroxidase (LiP) activities of around 2,000 U/l and 400 U/l were attained by the former, whereas the activities reached by the latter were of about 1,500 U/l and 200 U/l, respectively. Furthermore, laccase activity (around 150 U/l) was only detected in manganese (IV) oxide supplemented cultures.The polymeric dye Poly R-478 (0.02 w/v) was added to three-day-old cultures. A percentage of biological decolourization of about 85% was achieved using cultures supplemented with veratryl alcohol, whereas MnO2 cultures showed a rather lower percentage of around 58% after nine days of dye incubation. Moreover, a correlation between MnP activity and Poly R-478 decolourization could be observed, indicating that this enzyme is mainly responsible for dye degradation.In the present work, the in vivo decolourizing capability of the ligninolytic complex secreted by P. chrysosporium was investigated under the above-mentioned cultivation conditions, employing a model compound, such as the polymeric dye Poly R-478.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 53-64 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: An advanced primary treatment process for a municipal waste water was systematically studied, using a bio-flocculation-adsorption, sedimentation and stabilzation process (BSS). It was shown that the organic removal efficiency was higher than that of the traditional primary treatment processes but lower than that of the traditional secondary treatment processes. Both adsorption and bio-flocculation played an important role in the removal of pollutants. The activated sludge within the bio-flocculation-adsorption tank could be considered a bio-flocculent which improved the quality of the effluent from the primary treatment process. As the effluent of the BSS process did not meet the requirements for a typical secondary effluent, the process may be regarded as an advanced (or enhanced) primary treatment process, suitable for waste water containing a high concentration of suspended solids and colloidal particles.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 67-73 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The concentration of airborne fungal spores and bacteria as related to room temperature, humidity and occupancy levels within a library building in Singapore was determined. Measurement of indoor air quality with respect to microorganisms is of particular importance in tropical environments due to the extensive use of air-conditioning systems and the potential implications for human health. This study has revealed a number of interesting relationships between the concentrations of fungal spores and bacteria in relation to both environmental and human factors. The levels of fungal spores measured in the indoor environment were approximately fifty times lower than those measured outside, probably because of the lowered humidity caused by air-conditioning in the indoor environment. The variation in fungal spore concentration in the outdoor environment is likely to be due to the diurnal periodicity of spore release and the response to environmental factors such as light temperature and humidity. The indoor concentration of fungal spores in air was not clearly correlated to concentrations measured in air outside of the library building and remained relatively constant, unaffected by the difference in the numbers of occupants in the library. In contrast, the indoor concentrations of bacteria in air were approximately ten times higher than those measured outdoors, indicating a signficant internal source of bacteria. The elevated levels of indoor bacteria were primarily attributed to the number of library occupants. Increased human shedding of skin cells, ejection of microorganisms and particulates from the respiratory tract, and the transport of bacteria on suspended dust particles from floor surfaces probably accounts for the strong positive correlation between occupancy levels and the concentration of bacteria in internal air.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000) 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 96-96 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 87-96 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Preliminary results on the novel use of the bacterium Thiobacillus ferrooxidans (ATCCJ 3598 and ATCC33020) for the micro-machining (or biomachinig) of metals are reported. Biomachning is a controlled microbiological process to selectively form microstrucutures on a metal work-piece by metal removal (or dissolution) using microorganisms. Applying copper and mild steel as work-pieces, it was shown that the mass removed increased proportionately with machining time. In another experiment, the work-pieces were coated with organic photo-resistive materials to mask (i.e. protect) certain regions of the metlas, thereby defining the microstructure to be formed. The unmasked regions were successfully biomachined; the final machined profile was shown to be similar to the coating image on the original metal. Although biomachining proceeded at a slower rate than chemical machining, the undesired leaching of the metal in the region under the masked area (termed undercutting) was not as severely encountered when compared with the latter. This work demonstrates the potential use of microorganisms for the biomachining of metals. As a “green process”, the innovative use of T. ferrooxidans for the micro-machining of metals opens up the possibility of biomachining as an alternative to conventional metal processing.
    Additional Material: 5 Ill.
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  • 11
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: During the microbial treatment of a sandy model soil artificially contaminated with polycyclic aromatic hydrocarbons (PAHs), a large residual pollution was found. The remainig PAHs were sorbed into the micropores of the soil and were therefore not bioavailable. Using a lab-scale precolator, the microbially pretreated soil was subjected to aftertreatment with surfactants with the aim of further degradation of its pollution. Two commercial nonionic surfatants of the polyethoxylate type, Präwozell F1214/5 N and Sapogenat T-300, were used. The surfactants differ both in their physicochemical properties (CMC value, PAH solubilization capacity, adsorption onto soil) and in their microbial degradability. During aftertreatment under permanently aerobic conditions, only a weak PAH accumulation in the liquid phase was observed, which was due to a low solubilization rate as well as to simultaneous microbial degradation of the dissolved PAHs. Temporary anaerobiosis successfully suppressed the microbial degradation of both the surfactant and the solubilized PAHs, resulting in a more intensive PAH accumulation. But the PAH content of the soil - the essential criterion for evaluating the efficiency of surfactant application - was not decreased to a larger extent with surfactants than without them. To find out why the surfactants failed to act, the surfactant and hydrocarbon distribution among the liquid and solid phases was studied in mixtures of phenantherne-spiked solis and Präwozell-containig liquids; at heavy phenanthrene loading, the aqueous phase was saturated with PAH; at weak loading, it was unsaturated. Model-aided data analysis showed that the soil may contain PAH in two fractions: strongly sorbed into soil pores and, in the case of heavy loading, also weakly attached to the soil surface. The latter is easily extractable, resulting in a PAH-saturated liquid, while strongly adsorbed PAH is only partially dissolved due to competition between the micelles and the soil pores for the PAH. The microbially pretreated soil contains only strongly bound PAHs, which are as difficult to extract by surfactants as they are poorly accessible for microbes.
    Additional Material: 8 Ill.
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  • 12
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Autochthonous bacteriocenoses in semiarid soils in Patagonia were found to be capable of rapidly adapting to high contamination with crude oil. This adaptation at community level is due to the selective enrichment of hydrocarbon-utilizing bacteria always present in these soils. Immediately after a heavy contamination with crude oil, the authochthonous bacteriocenosis contained about 28% hydrocarbon-utilizing bacteria which could be classified into eight ecotypes with characteristic metabolic profiles. Mainly n-alkanes were used as growth substrates of representative strains. After seven months' exposure to crude oil, the bacteriocenosis consisted almost entirely of hydrocarbon-utilizing bacteria. At least fourteen ecotypes were distinguishable, and the majority of representative strains were able to metabolize a broad spectrum of aliphatic and aromatic hydrocarbons. Corresponding to the significant alteration of the physiological diversity, drastic changes to the taxonomic diversity were also found. Whereas at the beginning of the study the autochthonous bacteriocenoses were dominated by GRAM-positive genera of the Actinomycetales (Dietzia, Gordona, Nocardia, Rhodococcus, Streptomyces) with high ecological potency, after just two months' exposure to crude oil, GRAM- negative bacteria (especially Pseudomonas stutzeri) became predominant within the hydrocarbon-utilizing bacteriocenoses accompanied by some GRAM-positive genera of the Actinomycetales with a significantly lower abundance. These findings underline the importance of Pseudomonas and some genera of Actinomycetales for processes of natural attenuation and the technically supported in situ bioremediation of soil polluted by crude oil in Patagonia.
    Additional Material: 2 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 149-159 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Some parameters of the production of an alkaline protease by Rhizopus oryzae in the solid state fermentation of wheat bran were optimized. Using the optimum parameters of an inoculum age of 7 days, an incubation time of 9 days, an amount of CZAPEK-DOX (liquid medium) of 6 ml/g bran and an incubation temperature of 33°C, an activity of 50 U/g bran was achieved. The initial pH of the CZAPEK-DOX medium had little effect. Re-incubation of mouldy bran with only fresh CZAPEK-DOX yielded 3 times total activity compared to single-cycle fermentation. As for the effect of the amount CZAPEK-DOX medium, the water constituent contributed more to activity increase than did the salt component. The ARRHENIUS activation energies were 23 and 7.9 kcal/mole below and above the optimum of 33°C, respectively. In all the studies, along with protease production, variation of protein content and specific activity were also observed. Attempts were made to explain the effects and also gauge their implications for large-scale production.
    Additional Material: 4 Ill.
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  • 14
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000) 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 187-187 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 189-201 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Desulfovibrio vulgaris strain PY1 was isolated from a 3-chlorobenzoic acid (3CBA) degrading anaerobic enrichment culture, using anaerobic Percoll density centrifugation. When grown on pyruvate (20 mM), in the absence of sulphate and under strict anaerobic conditions, this organism converted not only the co-substrates benzoate (BA), 3-amino-BA and 3CBA to the corresponding alcohols but also ten other different halogenated benzoic acids, viz., 4-Cl-, 3-Br-, 4-Br-, 3-I-, 3-F-, 4-F-, 2,4-di-Cl-, 2,5-di-Cl-, 3,4-di-Cl- and 3,5-di-Cl-BA. This was verfied with HPLC and GC/MS spectrometric analyses. The yields of the co-substrate converted after 30 days of growth were between 20% and 88%, depending on the compounds which had been added at initial concentrations of 500 μM. Sulphate, sulphite, thiosulphate and disulphite inhibited the formation of 3-Cl-benzyl alcohol (3CBOH), i.e. a 97 to 99% inhibition, and nitrate and sulphur had no effect (a 7-10% inhibition). In cell-free extracts, the reduction of 3CBA to 3CBOH required strict anaerobic conditions, pyruvate or H2 as electron donors and the addition of methylviologen (MV), FAD, FMN or ferredoxin as electron carriers. The specific activity of the reduction of 3CBA to 3CBOH in crude extract was 5.3 nmol/(mg protein min). The reaction was not inhibited by additions of sulphate or sulphite (5 mM), but was completely inhibited at concentrations of 10 mM 3CBA or 50 mM BA. A carboxylic acid reductase (aldehyde dehydrogenase), which acted on non-activated 3CBA and was responsible for the reduction of 3CBA to 3-Cl-benzaldehyde, was found in the solube fraction (94% of the total activity). These results demonstrate that strain PY1 was able to effectively reduce a wide range of halogenated benzoic acids to the corresponding alcohols.
    Additional Material: 3 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 203-218 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The recent upsurge in information technology has provided the international community with an easy access to professional journals (e.g. Electronic Journal of Biotechnology at http://www.ejb.org; etc.), discussion groups (e.g. bioenergy@cret.org; digestion@crest.org; etc.) and recently to electronic international conferences (e.g. ICIBS; http://www.cid.harvard.edu/cidbiotech, etc.) as well as a series of biotechnological information material (e.g. http://www.psrast.org, etc.) to stay in contact and receive up-to-date information in biotechnology. There is no doubt that this new technology will be more cost effective in future and reach more people in communities around the globe.This review reports on one such an electronic conference aiming at bridging the communication gap between developed and developing countries. This conference dealt with integrated biosystems and has provided an excellent forum for more than 100 active participants from all regions of the world. As has been demonstrated in this review, the conference was able to show the very different approaches towards the use of biotechnology in developed and developing countries, cold and tropical climate regions owing to their different ecological, economical and societal problems. It also demonstrated very clearly that the field of molecular genetics and/or genetic engineering is not a priority issue in developing countries, but rather the need for clean technologies, multiproduct formation through socio-economic integrated biosystems, e.g. incorporating microbial waste management into agro-industries, in human activities and their roles in creating better health conditions, a better environment and sustain development.It is hoped that this review will lead to a greater use of the electronic facilities available to inform and educate both the northern and the southern communities more readily of their needs and requirements to improve understanding and efforts for a sustainable future.
    Additional Material: 4 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 275-288 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The purpose and scope of this article is to introduce capable zeolites into downstream processing of natural compounds, especially flavour compounds like 2,5-dimethyl-4-hydroxy-3(2H)-furan-3-one (Furaneol®Furaeol is a registered trademark of FIRMENICH, Ch). The synthesis and the recovery of Furaneol from L-rhamnose are presented. Therefore adsorption isotherms of the zeolites ZSM5 and DAY with varying modules have been determined and adsorption experiments using model and reaction mixtures of Furaneol synthesis were performed and will be discussed.
    Additional Material: 11 Ill.
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  • 20
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: A fermentation process for manufacturing 1,4-piperazinium-(L,L)-dilactate from renewable raw materials and a method for processing this product into L,L-dilactide are described. Lactic acid fermentation with Lactobacillus paracasei was modified in such a way that pH control occurred by using an aqueous solution of piperazine as a correcting agent instead of sodium hydroxide solution. The production of a stoichiometrically composed piperazinium lactate was possible when the pH was 5.0. From 5.0 kg of glucose and 2.15 kg of piperazine, 6.65 kg of 1,4-piperazinium-(L,L)-dilactate were formed in the fermentation process. Separation from fermentation broth, purification and concentration of the product in aqueous solutions were carried out by means of ultrafiltration, nanofiltration and electrodialysis. Total product retention by the membranes used was about 33%. The crystalline salt was obtained by vacuum evaporation. Processing of the 1,4-piperazinium-(L,L)-dilactate into L,L-dilactide was performed in a special glass reactor. A product yield of 70% was achieved. The purified product was characterized by elementary analysis, as well as solubility behaviour, polarity and spectroscopic data. An overall process consisting of the stages fermentation, purification and concentration of piperazinium dilactate as well as cyclization of the latter to dilactide is described.
    Additional Material: 9 Ill.
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  • 21
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Because of the growing utilization of renewable raw materials, the technical use of lignocellulosic fibres from wood and other annual plant materials is becoming increasingly important. The conventional production process of fibreboards is characterized by high-energy consumption and use of ecologically insecure synthetic lesins. Approximately 40 to 45% of the total energy expenditure are used for the thermo-mechanical pulping. Because of high plastication temperatures, an inactive lignin crust on the fibre surface is formed. For that reason, for glueing of the fibres, urea formaldehyde and melamin resins are usually used. The costs for the resin amount to approximately 50% of the entire material costs. In addition, environmental problems are caused. The aim of our investigation is the reduction of energy and resin consumption by enzymatic modification of wood chips and the enzymatic activation of the inherent bonding strength of the material. The first industrial use of fungi for the modification of wood was in the production of “Myco wood”. Pleurothus ostreatus and Trametes versicolor were applied for nonsterile delignification of beech wood. The present investigation of the authors deals with the mycological pre-treatment of wood chips in order to reduce the energy consumption during wood pulping. The screening results favour the brown rotter Gleophyllum trabeum for pinewood (Pinus silvestris) and the white rotter Trametes hirsuta for beech (Fagus silvatica). Both species show resistance against mould fungi. The use of submerged inoculum of these fungi has the advantage over wheat inoculum that the lag phase is less than 12 hours and that the addition of nutrients or fungicides is not necessary. Short-time wood chip incubation results in a 40% decrease of energy consumption during thermo-mechanical pulping and in improved fibreboard properties. Lignin reduction could not be determined by gravimetrical and x-ray microanalysis.Comparative investigations of fibre incubation using laccase, a submerged culture of Trametes versicolor and rape straw fibres show a high increase in bending and tensile strength and an improvement in the hygroscopic properties of glue-free fibre boards for the last two incubation kinds. Similar effects have been obtained incubating pine wood fibres for the production of fibre sheets with enzyme medium of Trichoderma reseei.
    Additional Material: 4 Ill.
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  • 22
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 335-350 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: During the 20th century, important relationships developed between the oil industry and both microbiological and biotechnological research. Basic microbiological research has played an important role in both the exploration and production sectors of the oil industry, but as the maturity of the industry has progressed, such contributions have been relegated with respect to their importance. With respect to refining and petrochemicals manufacture, process routes have been extensively researched, but only rarely have the biotechnological solutions developed satisfied the economic criteria that resulted in major investment. In fact, situations exist where investment has occurred, but project life was unrealistically short, suggesting a need for extreme caution when evaluating biotechnological processes for the oil industry. However, as far as engineered processes for both biotreatment and bioremediation are concerned, the fundamental research that has underpinned other areas of hydrocarbon microbiology will finally prove to be of both technical and economic value, in ensuring that the essential needs of treatment, rather than disposal, and restoration, rather than environmental destruction, can be satisfied by the oil and other industries involved in both geochemical manipulation and natural resource exploitation.
    Type of Medium: Electronic Resource
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  • 23
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The influence of different growth-limiting factors - namely the sources of carbon, nitrogen and phosphorus and the dilution (growth) rate - on the ice-nucleation activity of Pseudomonas syringe CCM 4073 was studied. A higher ice-nucleation activity was observed at a lower dilution (growth) rate (D = 0.1 h-1) than at a higher dilution (growth) rate (D = 0.3 h-1). Remarkable differences in ice-nucleation activity were found in its dependence on the growth-limiting factor. The highest ice-nucleation activity was observed under carbon limitation (T90 = -2.7°C), a medium activity under nitrogen limitation (T90 = -5°C) and lowest activity under phosphorus limitation (T90 = -12.3°C). After the addition of excess nitrogen or phosphorus to steady-state cultures, the ice-nucleation activity was restored.
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  • 24
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Continuous counter-current chromatographic processes have been successfully used in the petrochemical and sugar industry over the last 30 years. Only recently has simulated moving bed (SMB)-technology attracted widespread interest in the pharmaceutical industry, mainly as a very efficient system for chromatographic enantioseparation. The application of this technique to the downstream processing of biotechnological products requires some specific changes to meet the special demands of bioproduct isolation. Production processes are set up on an multi-ton scale, for example, for the purification of fructose with both yield and purity higher than 90%. Examples for other mono- and oligosaccharides are reported. In the purification of fatty acids or fat soluble vitamins, SMB technology under supercritical fluid conditions gives additional benefits and increases the productivity by a factor of four when a pressure gradient is applied. Another field of operation is the isolation of drug compounds from natural sources where different batch- and SMB-chromatographic steps could be successfully combined. First examples are reported for cyclosporine A and paclitaxel isolation. Finally, step-gradient elution modes can be used continuously, as demonstrated for the isolation of monoclonal antibodies.
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  • 25
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 26
    Electronic Resource
    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 65-65 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 27
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 28
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    Electronic Resource
    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 41-52 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Studies were carried out to evaluate the feasibility of using coffee industry residues, viz. coffee husk, coffee leaves and spent coffee ground as substrates in solid state fermentation (SSF) to cultivate edible mushrooms Pleurotus. Eight strains of Pleurotus ostreatus and two strains of Pleurotus sajor-caju were screened on a medium prepared from aqueous extract of coffee husk and agar. Based on best mycelial growth (9.68 mm/day) and biomass production (43.4 mg/plate in 9 days at 24°C), the strain P. ostreatus LPB 09 was selected for detailed studies. SSF was carried out using these substrates under different moisture conditions (45-75%) and spawn rates (2.5-25%). In general, although a 25% spawn rate appeared superior, the 10% spawn rate was recommended for all the three substrates in view of the process economics, as there was not any significant difference in the increase with 10 to 15%. The ideal moisture content for mycelial growth was 60-65% for coffee husk and spent coffee ground, and 60-70% for coffee leaves. The biological efficiency (BE), which is defined as the ratio of the weight of fresh fruiting bodies to the weight of dry substrate, multiplied by 100, and which indicates the fructification ability of the fungus for utilizing the substrate, was best with coffee husk. With coffee husk as the substrate, the first fructification occurred after 20 days of inoculation, and the biological efficiency reached about 97% after 60 days. When coffee leaves were used as the substrate, no fructification was observed even upon prolonged cultivation. With spent ground as the substrate, the first fructification occurred 23 days after inoculation and the biological efficiency reached about 90% in 50 days. There was a significant decrease in the caffeine and tannin contents (61 and 79%, respectively) of coffee husk after 60 days. It was remarkable to observe that caffeine was adsorbed onto the fruiting body (0.157%), indicating that it was not completely degraded by the fungal culture. However, no tannins were found in the fruiting body, indicating that the fungal strain was capable of degrading them. The results showed the feasibility of using coffee husk and spent coffee ground as substrates without any pre-treatment for the cultivation of edible fungi in SSF, and provided one of the first steps towards an economical utilization of these otherwise unutilized or poorly utilized residues.
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  • 29
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 75-81 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Serratia marcescens biovar A2/A6 is able to produce a red pigment as a secondary metabolite which has antimicrobial activity. This paper describes its growth and biopigment formation in batch cultures, in media containing different concentrations of lactic acid and beef extract as carbon and nitrogen sources, respectively. An unstructured model has also been developed to describe its growth, lactic acid uptake and biopigment formation. The comparison of simulated and experimental data shows that the proposed model predicts reasonably well the system behaviour over a range of conditions.
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  • 30
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 97-98 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 31
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The increasing requirements in wastewater treatment have led to the development of new wastewater treatment processes based on the know-how and experience in reaction and process engineering of the chemical industry. Due to their compactness, closed operation and high flexibility, these new processes show a large potential for process integration and significant cost reduction in particular for highly polluted industrial wastewaters.This paper discusses the HCR (high-performance compact reactor) - process, developed at the Mass Transfer Laboratory of the Technical University of Clausthal within the last decade. This process has been realized in more than 30 technical applications with a volume loading of up to 70 kg COD/m3 d and an energy consumption of about 0.4 kWh per kg CODelim.
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  • 32
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 33
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 34
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 161-168 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Five different chemical reagents and γ-rays were tested for the sanitization of immobilized biocatalysts with high penicillin G acylase (PGA) activity. The most effective chemical reagents were N-cetyl-N,N,N-trimethylammonium bromide (CTAB) and 2-isopropyl-5-methylphenol (thymol). The optimum concentration of CTAB for the treatment of the immobilized enzyme was 0.25% [w/v] and 1 h, for immobilized cells 0. [w/v] and 3 h. The optimum concentration of thymol for the immobilized enzyme was found to be 0.1% [w/v] and 1 h, for immobilized cells 0.27% [w/v] and 2 h. The optimum dose of γ-rays for the sanitization of the immobilized enzyme was established as 3.2 kGy, for immobilized cells as 4.5 kGy.
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  • 35
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 169-174 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Nitrogen fixing Anabaena azollae strains isolated from four different Azolla cultures were characterized based on their total protein profile and RAPD profile to study the existing variation among them. As expected, the isolates showed almost similar protein banding patterns, but exhibited differences in 40-70 KDa protein subunits. Polymerase chain reaction of the DNA of the isolates, using four different primers, amplified specific sequences of DNA and showed clear polymorphism among the isolates. The RAPD profile generated the fingerprinting pattern characteristic of each strain based on the sequence of the primers used. Common band sharing observed between the strains A. azollae-RS-KK-SK-AM and A. azollae-RS-KK-SK-RP probably represents maternal inheritance of DNA to the progeny. The polymorphic bands were generated specifically for the isolates A. azollae-RS-KK-SK-RP and A. azollae-RS-KK-SK-AM with primers numbered 2 and 4, respectively, which could be developed as possible markers for these isolates.
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  • 36
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 175-183 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Mature seed-derived callus from an elite Chinese japonica rice cv. Eyl 105 was transformed with a plasmid containing the selectable marker hygromycin phosphotransferase (hpt) and the reporter β-glucuronidase (gusA) genes via particle bombardment. After two rounds of selection on hygromycin (30 mg/l)-containing medium, resistant callus was transferred to hygromycin (30 mg/l)-containing regeneration medium for plant regeneration. Twenty-three independent transgenic rice plants were regenerated from 127 bombarded callus with a transformation frequency of 18.1%. All the transgenic plants contained both gusA and hpt genes, revealed by PCR/Southern blot analysis. GUS assay revealed 18 out of 23 plants (78.3%) proliferated on hygromycin-containing medium had GUS expression at various levels. Genetic analysis confirmed Mendelian segregation of transgenes in progeny. From R2 generations with their R1 parent plants showing 3:1 Mendelian segregation, we identified three independent homozygous transgenic rice lines. The homozygous lines were phenotypically normal and fertile compared to the control plants. We demonstrate that homozygous transgenic rice lines can be obtained via particle bombardment-mediated transformation and through genetic analysis-based selection.
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  • 37
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 202-202 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 38
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 219-233 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The GRAM-positive bacterium Rhodococcus erythropolis K2-3 and the GRAM-negative Ochrobactrum anthropi K2-14 are capable of synergistically degrading 4-(2,4-dichlorophenoxy)butyric acid (2,4-DB). The two strais execute this task in a symbiotic manner, but the nature of the interaction involved in the degradation is only partially understood as yet. An essential first step in elucidating the interaction is to be able to monitor the two strans separately, at the cellular level, within mixed populations. Therefore a method exploiting fluorescently labelled lectin probes was developed. Since Concanavalin A (Con A) binds specifically to R. erythropolis K2-3, it was selected and linked to the fluoresent dye Bodipy 630/650, which has an excitation maximum in the red part of the visible light spectrum. Forward light scatter (FSC) and DNA fluorescence from both strains were also measured to obtain simultaneous information about their physiological states. The three parameters were conveniently monitored by dual and triple excitation flow cytometry in conjunction with double fluorescent staining techniques. In addition, the strains were identified using an epifluorescence microscope. These techniques were found powerful tools for the population analysis of this mixed bacterial system.
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  • 39
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 40
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 235-274 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: A quite unconventional, innovative scientific methodology called “macroscopic pattern analysis” is presented in this paper. This approach is more adequate in the case of complex systems than the well-known microscopic, mechanistic approach. Complex systems are not only attracting more engineering interest, but their scientific treatment is increasingly wanted by society due to the manifold problems in Earth's ecosphere. The macroscopic pattern approach will be explained in depth and illustrated in some case studies from the ecosphere (sustainability, hurricanes and avalanches), where nature serves as a teacher for the solution of the sustainability problem. Then, a series of case studies on macropatterns are described showing the problem-solving capacity for anthropo- and technosphere: sustainability in society with an index of sustainability, the eco-social market economy with eco-tech as an instrument, biokinetics, bioreactor mixing and integrated bioprocessing with models, design of cars and houses and even quality of life as an attempt to quantify macropatterns.The innovations are briefly compared in their problem-solving capacity with known approaches such as the microscopic method in science, technology and society (free market economy), including the evaluation of other indices and cleaner production, industrial ecology and zero emission initiative. Finally, a deeper integration of sciences, ethics, arts and nature will be introduced based on the vision with macroscopic pattern analysis, where the different domains of human life are integratable to effect a reconciliation.
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  • 41
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 334-334 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
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  • 42
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The impact of hydrocarbon remediation on several enzyme activities (catalase, dehydrogenase, lipase, protease, urease, alkaline phosphomonoesterase, fluorescein diacetate hydrolysis) and microbial properties (biomass-C, respiration, N-mineralization, qCO2, microbial counts) was evaluated in a laboratory study over a period of 10 weeks. A pristine soil was contaminated with diesel oil (10 mg/g soil) or with a mixture of phenanthrene and naphthalene (total amount 1 mg/g soil) and supplemented with inorganic nutrients to give a C:N ratio of 20:1. The corresponding controls consisted of uncontaminated nutrient-supplemented soil. Oil contamination caused a significant initial increase of all biological parameters measured. In the presence of PAHs, biomass-C, respiration, protease activity and heterotrophic counts were significantly enhanced, while urease activity was depressed. N-mineralization was initially, however, reversibly inhibited in the presence of oil and PAHs.The measured parameters behaved differently over time: Biomass-C, respiration and alkaline phosphomonoesterase activity reached a maximum activity after about 2-5 weeks, corresponding to the period during which the majority of hydrocarbons disappeared, and declined thereafter to the background level. Activities of catalase and dehydrogenase also followed this pattern, however, were characterized by fluctuations. Activities of lipase, protease, urease and fluorescein diacetate hydrolysis increased and remained almost constant throughout the incubation period.
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  • 43
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    Berlin : Wiley-Blackwell
    Acta Biotechnologica 20 (2000), S. 351-368 
    ISSN: 0138-4988
    Keywords: Life Sciences ; Life Sciences (general)
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: The action resonance theory (ART), a hypothesis based on a logical extension of EINSTEIN's theory of Brownian movement, suggests that the genotype × environment interaction can be modelled as forceful encounters of the gene-products of an organism with its environment. This model has implications for molecular and cell biology, morphogenesis, evolutionary development via mutation, the mechanism of natural selection and overall function of ecosystems, extending SCHRÖDINGER's programme for molecular biology. Action, a thermodynamic property with the same physical dimensions as angular momentum and PLANCK's quantum of action, is proposed to be reversibly generated as a result of the molecular exchange of quanta, which become resonant at equilibrium, corresponding to an optimum degree of entropy and action for living systems. Because the theory can potentially predict solutions to unsolved problems such as the folding of proteins it has strong implications for successful genetic modification of organisms and for biotechnology in general; the design of a programme of research to test this theory is proposed. A key element in this research programme, improving productivity and sustainability, would be the need to select genetically modified strains in the ecological environment or niche in which they are required to function.
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  • 44
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The antibiotic chlorotetracycline (CTC) is used as a fluorescent chelate probe to investigate its active transport in respiring Staphylococcus aureus cells. CTC chelation to magnesium or calcium leads to fluorescence enhancement. This enhancement is further increased when the polarity of its environment is decreased, as occurs when the complex moves from an aqueous environment into a membrane. Upon addition of CTC to a dispersion of S. aureus cells, a time dependent fluorescence enhancement is detected which is a monitor of the transport of the CTC-divalent cation complex into the membrane. This uptake has been shown to be energy dependent and exhibits saturation kinetics with an apparent Km of 107 ± 20 μM by the same technique. The initial rates of antibiotic uptake are shown to have a pH optimum between 5.5 and 6.5. The effects of exogenously added EDTA and paramagnetic Mn2+ indicate that the CTC-divalent cation complex is transported to the inside of the membrane. Exogenously added magnesium inhibits the accumulation process. This implies that the membrane CTC binding site involves a divalent cation sequestered away from the surface of the membrane, and only free CTC is bound to that site. The uptake of CTC is also temperature dependent with a maximal rate at 40°. Arrhenius plots of the initial fluorescence enhancement rates are found to be biphasic with a 27° transition temperature. The break in the plots presumably reflects an order-disorder transition involving the fatty acids of the cell membrane. Thus, transport of the CTC involves movement through the fatty acid region of the membrane. This movement is facilitated by the more fluid state of the membrane above the transition temperature.
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  • 45
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974) 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 46
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 108-120 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 4 Ill.
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  • 47
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 163-165 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 48
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 189-195 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 5 Ill.
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  • 49
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: In part I of this paper (1) we give evidence that the P23-capsoid of τ-particles is transformed in situ into the P23*-capsid of normal phage. Using the polymorphism of phage T4, we have chosen polyheads as representative of P23 assemblies and giant phages as representative of P23* assemblies in order to study their surface crystals by optical filtration of micrographs. We found for polyheads a lattice constant of 112 Å with the typical hexameric, ringlike capsomer and for the giants a lattice constant of 124 Å with quite a different capsomer morphology, of the type (6+1). From the stoichiometry of the proteins composing the normal capsid we conclude that the protomer is a single P23* molecule and that the minor capsid-proteins must be in singular positions on the surface lattice or on the polyhedral head (center of capsomers, vertices, or basal part).We extrapolate the findings on the giant head to the normal head and give a geometric model which is consistent with 1,100 molecules of P23* per capsid.We discuss the part of form inheritance contributed by P23 and the other formgiving gene products and give evidence that morphologic characters are the result of pairs of a reaction chain of interacting gene products. The example we give is the giant head produced by a ts mutant in gene 24 at 36°C.
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  • 50
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 496-511 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Enveloped viruses which form by budding at the cell surface possess a membrane consisting of a lipid bilayer and a small number of virus-coded polypeptides. Since viral polypeptides become integral components of the plasma membrane during assembly, the process of synthesis and incorporation into membranes of these proteins may reflect the pathway of plasma membrane assembly. Electron microscopic studies have suggested that viral envelope proteins are incorporated into discrete, localized regions of the plasma membrane which serve as recognition sites for the viral nucleocapsid. In influenza virus-infected cells, viral polypeptides are associated with cytoplasmic membranes as well as the plasma membrane. The major envelope glycoprotein appears to be synthesized in rough endoplasmic reticulum, and to migrate to smooth membranes after synthesis. Glycosylation is initiated in rough membranes and progresses further in smooth membranes. Unlike the glycoproteins, the major nonglycosylated polypeptide appears to be inserted directly into the plasma membrane. In the presence of 2-deoxyglucose or high concentrations of glucosamine, aberrant viral glycoproteins are detected which appear to be unglycosylated or partially glycosylated; these are associated with membranes and incorporated into virus particles of reduced infectivity. Therefore normal glycosylation is not essential for incorporation of viral glycoproteins into cellular membranes or virus particles, but is required for normal biological activity. The role of the viral neuraminidase in assembly and release has been studied using mutants defective in neuraminidase at restrictive temperature. Under these conditions virus formation occurs, but the progeny form large aggregates at the cell surface. Colloidal iron hydroxide staining indicates that such virus particles contain neuraminic acid, and these residues appear to serve as receptors leading to the extensive aggregation.
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  • 51
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    Journal of Supramolecular Structure 2 (1974), S. 166-177 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The assembly of E. coli ribosomes has been studied through the analysis of a new group of ribosome maturation mutants. These mutants, all blocked in a late stage in the maturation of 50S ribosomes, map at four different sites on the chromosome. These sites are distant from the known ribosomal protein sites at the str-aro E region of the chromosome. The ribosome precursor particles of the mutants contain precursor-type 23S RNA (p23 RNA) and 5S RNA. 43S particles of one of the mutants contain all but one of the normal complement of proteins. Precursor 43S particles from this mutant can be converted to particles with sedimentation values around 50S by incubation with extracts from either the wild-type organism or from other mutants. This in vitro conversion process differs considerably from the process of ribosome reconstitution and indicates a role for extrinsic factors in the maturation of E. coli ribosomes.
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  • 52
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 302-317 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 9 Ill.
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  • 53
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    Journal of Supramolecular Structure 2 (1974), S. 318-328 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: When phage DNA is added to an extract of an induced lambda lysogen, complete phage particles are made that contain the added DNA. The DNA substrate for packaging is a covalently joined polymer of several phage units. Unjoined units must first be joined by DNA ligase in the extract. Therefore DNA cutting is a necessary part of the DNA packaging reaction. The protein product of gene A, called A protein, behaves like the enzyme that cuts DNA and is a necessary component of the extract.Three of the head proteins preassemble into a spherical shell that subsequently combines with DNA. These shells are made of E protein, the major protein of a finished head, and they can be the sole source of that protein. They also contain a few molecules of two processed proteins, fused C-E and cleaved B. The processing may be essential for assembly because other shells that contain C protein not fused and B protein uncleaved are less than 1% as active.Protein A and DNA first react with the protein shells, then D protein, the second most abundant head protein, is added. These new observations are combined with published data to develop a comprehensive view of λ head assembly.
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  • 54
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    Journal of Supramolecular Structure 2 (1974), S. 670-681 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Detergent-solubilized proteins and lipids of mycoplasma membranes reassemble spontaneously into membranous structures on the removal or dilution of the detergent in the presence of divalent cations. The cations seem to function by neutralizing the negatively charged groups on membrane lipids and proteins which interfere by electrostatic repulsion with membrane reassembly. Moreover, salt bridges formed by the divalent cation between acidic groups on membrane proteins and lipids seem to play an important role in the reconstituted membrane stability. Electron transport activity, as measured by the transport of electrons from NADH to oxygen, has been demonstrated in reconstituted Acholeplasma laidlawii membranes. However, restoration of active transport of sugars or ions has not been achieved so far. The conditions for obtaining properly sealed vesicles, which are obligatory for demonstrating transport activity, are still rather poorly defined. The reassembled membranous structures cannot be distinguished from the native membranes in chemical composition, density, and thin sections. However, probe techniques, x-ray diffraction, and freeze-fracturing electron microscopy indicate that the proteins are organized differently in the reassembled membranes, though the lipid bilayer is restored. The results obtained so far leave little hope for successfully reconstituting the molecular organization of membranes as complex as those of mycoplasmas by a single-step reassembly of detergent-solubilized membrane components. The prospects appear brighter with membranes having only a few protein species, such as the outer membrane of gram-negative bacteria. In spite of the failure to reconstitute fully active mycoplasma membranes, the reassembly procedure was found valuable in studying the interactions of detergent-solubilized membrane proteins with lipids, the effects of a hydrophobic environment on hydrophilic enzymes, and the production of “hybrid” membranes having selected membrane components.
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  • 55
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 728-736 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Tritium-labeled cytochalasin B binds rapidly and reversibly to mammalian cells, and a class of high-affinity sites (Kn ≅ 10-7 M) and a class of low-affinity sites (KD ≥ 10-5 M) are detected. In red blood cells, the high-affinity binding sites (about 3 × 105 per cell) are associated with the plasma membrane, and at least 80% of these appear to be intimately related to the glucose transport system. Fractionation of cellular components of platelets by differential centrifugation and gel filtration chromatography reveals that the high-affinity binding sites in these cells are also associated with membranous materials. A substantial number of the low-affinity binding sites can be traced to platelet actin. The binding of cytochalasin B to actin is consistent with the alteration of intrinsic viscosity and morphology of actin filaments in vitro by the compound at concentrations of around 10-5-10-4 M. The interaction of cytochalasin B with actin may account for its inhibitory effect on various forms of cell motility.
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  • 56
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    Journal of Supramolecular Structure 2 (1974), S. 121-137 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 12 Ill.
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  • 57
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    Journal of Supramolecular Structure 2 (1974), S. 150-162 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have purified actin and my osin-like proteins from amoebae of Dictyostelium discoideum. These proteins are very similar in their physical and enzymatic properties to muscle actin and myosin. Most importantly, they form thin and thick filaments, respectively, and Dictyostelium actin activates Dictyostelium myosin ATPase activity. Actin from these amoebae appears to be identical in size to muscle actin. The Dictyostelium myosin consists of two heavy chains of about 210,000 daltons and two classes of light chains, about 18,000 and 16,000 daltons. The heavy chains are slightly larger than those of muscle myosin. Biochemical and structural studies of membrane association of the contractile complex suggests that some of the amoeba actin is membrane-bound and acts as an attachment point for myosin and other actin filaments.
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  • 58
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    Journal of Supramolecular Structure 2 (1974), S. 225-238 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Phage P22 is known to have a linear duplex chromosome which is circularly permuted and terminally repeated. The propagation of these features of the mature phage DNA is accounted for by the fact that phage DNA lengths (headfuls) are cut from an intracellular intermediate form of phage DNA several phage genomes in length (concatemer) as first suggested by Streisinger. Studies with mutant phages show that cutting of concatemer DNA is intimately connected to the morphogenesis of the phage head.We have also found, by constructing a partial denaturation map of mature P22 DNA, that circular permutation in P22 DNA is restricted: all of the ends of the mature DNA fall within 20% of each other on the physical map. The limited distribution of ends can be explained by Streisinger's “headful” packaging model with the additional specifications that: a. the intracellular precursor DNA is no longer than ten times the length of mature phage DNA; b. encapsulation of DNA starts at a unique site; c. encapsulation proceeds sequentially therefrom.This model is supported by the distribution of molecular ends in denaturation maps of two deletion phage DNAs. We found, as expected from our model, that the extent of permutation is a direct function of the length of terminal repetition.
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  • 59
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    Journal of Supramolecular Structure 2 (1974), S. 239-252 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Mutants in gene U of phage λ produce polytails. Those polytails have a tail fiber and a basal part like normal tails, but their major tubular part is longer than that of normal tails and shows a wide length distribution.We established the morphogenetic pathway of the λ tail and found that U gene product (pU) acts throughout the assembly of the major tail protein (pV). Polytails in U- lysate are activated by pU in vitro and form long-tailed phage which are infectious to a small extent.If the formation of the basal part of the tail is blocked, pV (the major tail protein) remains unassembled as long as pU is present in the cell. However, we found that part of pV assembles into giant polytubes of several microns in length in lysates of a double mutant U- · H- in which both the basal part and pU are absent.pV in purified tails can be dissociated into disks (about 10S) or smaller units (about 2.5S) in vitro under extreme conditions. The disks form polytubes efficiently under physiological conditions, but the smaller units do not form polytubes efficiently. The smaller units have in vitro complementation activity with V- lysate. In vitro complementation activities with V-, U-, and Z- lysates are detected in the dialyzed extracts of SDS gel electrophoresis of purified tails. The molecular weights of the polypeptide chains containing those activities are estimated to be 31,000, 14,000 and 20,000 daltons, respectively.
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  • 60
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    Journal of Supramolecular Structure 2 (1974), S. 372-384 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Formation of a flagellar filament of Salmonella from its component protein, flagellin, is in principle a self-assembly process, which proceeds by the addition of flagellin monomers one by one to the distal end of the filament. Upon their polymerization, a conformational change of flagellin molecules occurs, and it confers polarity to the filament. For the initiation of in vitro flagellin assembly in a solution of physiological ionic strength and pH, it is essential to add fragments of flagellar filaments, which work as seeds for the polymerization of flagellin monomers. When an appropriate concentration of some anion known as a good salting-outer is added to the solution, the polymerization begins without addition of seed. Assembly of flagellins in vivo begins at the distal end of each hook. The distal ends of the hooks on the cells of a flagellin-less mutant were shown to initiate the assembly of exogenous flagellin in vitro, although the efficiency was not as high as that of the in vivo initiation. A flagellar filament elongates in vitro at a constant rate as long as a sufficient amount of flagellin is supplied, and the elongation terminates by an error occurring at the growing end of the filament. On the contrary, the rate of in vivo elongation decreases exponentially with increase of the length of the filament. Initial rate of the in vivo elongation depends on growth condition of the bacteria, while decrease of the rate per unit filament length is little affected by the growth condition. The observed limit in length of the flagellar filaments on growing bacteria is expected from the exponential decrease of their rate of elongation. The decrease of the in vivo elongation is correlated with the lowering of the transportation efficiency of flagellin monomers on their passage from the cell body through the central canal of a flagellar filament to the tip.
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  • 61
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    Journal of Supramolecular Structure 2 (1974), S. 393-411 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Tubulin obtained from disassembly of microtubules at 0°C exists in two forms: 6-S tubulin and a larger, curved or ring-shaped filament. These two forms have been separated chromat ographically and their roles in assembly examined. The purified rings reassemble to microtubules with high efficiency by uncoiling and straightening out, to be incorporated directly as protofilaments in the microtubule wall, and are thus identified as preformed protofilaments. Purified 6-S tubulin has not been observed to reassemble into microtubules by itself but will contribute to assembly when mixed with rings. Addition of glycerol at 0°C induces the 6-S tubulin to form rings, and the treated fraction will then reassemble to microtubules. Electron microscope observations indicate that assembly begins with the formation and growth of an incomplete microtubule wall. This wall grows wider by the addition of new protofilaments until the intact, circular microtubule, with 13 protofilaments, is formed. It is suggested here that growth of this wall from individual 6-S tubulin subunits may be energetically unfavorable. The direct incorporation of preformed protofilaments may be much more favorable, in which case the rings would be required for this initial stage of assembly.
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  • 62
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    Journal of Supramolecular Structure 2 (1974), S. 429-450 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Microtubule polymerization in vitro was examined using material purified from porcine brain tissue by a reversible temperature dependent assembly procedure, and was characterized by electron microscopy, viscometry, and sedimentation. The reaction was endothermic, colchicine sensitive, and occurred at neutral pH and moderate ionic strength. Divalent cations (calcium, magnesium) were inhibitory at millimolar concentrations, but stimulated polymerization at the micromolar level. Nucleoside triphosphates were required for assembly of purified subunits. As determined by quantitative sedimentation analyses, the reaction was an equilibrium process. Below a critical concentration of tubulin no assembly occurred. Analytical ultracentrifugation studies indicated that tubulin species with sO20, w of 6S and 30S were in equilibrium with each other, and that both were incorporated into microtubules. Electron microscopic analyses suggested that disc (or ring) structures might be intermediates in assembly, and that they were primarily utilized early in the polymerization process. Assembly could be seeded by mixing microtubular fragments from brain or flagella with brain microtubule subunits; depending on conditions of temperature and protein concentration, addition of subunits occurred either with unipolar or biased polar directionality. The possible significance of these properties of the polymerization reaction for control of assembly is discussed.
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  • 63
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    Journal of Supramolecular Structure 2 (1974), S. 451-465 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Beef brain tubulin isolated by cycles of polymerization and depolymerization contains two components, 6S subunit and a 25-35S boundary containing ring-shaped aggregates of tubulin. The rings disappear during microtubule polymerization, and the incorporation of ring tubulin into microtubules has been investigated by studying the changes in the sedimentation of tubulin which occur during polymerization. The “30S” boundary was separated from the 6S boundary by sedimentation at low temperatures. The temperature was then raised by letting a small amount of air into the vacuum chamber and the changes in sedimentation rate and concentration of each component determined as the tubulin polymerized. The 30S material polymerizes preferentially as determined by its decrease in concentration at polymerizing temperatures. Simultaneously with its decrease in concentration the 30S also decreases in sedimentation rate. The decrease in concentration of the 30S correlates well with polymerization while the decrease in sedimentation rate can occur independently of polymerization. The results indicate that the rings are not transformed directly into microtubules, but break down into subunits or small aggregates and these then assemble into microtubules. The rings may serve as a “storage aggregate” of active subunits. The presence of a possible storage aggregate in a dividing cell, the eggs of the surf clam, Spisula solidissima, has been indicated by measurements of particulate tubulin changes during the cell cycle. Microtubule assembly in vitro in homogenates of these eggs indicates that the amount of tubulin which forms microtubules may be controlled by the functioning of the microtubule organizing center.
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  • 64
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    Journal of Supramolecular Structure 2 (1974), S. 751-768 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Phytochrome (P), a chromoprotein of 120,000 MW, occurs at low concentrations in all higher plants. The chromophore is an open tetrapyrrole. The pigment exists in two light-absorbing forms: Pr, which absorbs at 660 nm, and Pfr, which absorbs at 730 nm. These forms are interconvertible by light. Pr, the physiologically inactive form, exists in dark-grown plants; Pfr, the active form, appears after irradiation with red light, P-mediated responses, of which about 80 are known, range from short-time effects (sec) such as bioelectric potentials, to long-time effects (hr) such as increases in enzymatic activity. Measurements of phototransformation in vivo with polarized light suggest that P is localized in the plasma membrane. Particulate cell fractions contain about 70% of total extractable P if Pfr is present and only 4% if Pr is present. Evidence indicates that the fraction containing Pfr may be the plasma membrane. One can isolate a partially solubilized membrane system, which can be reversibly reconstituted by adding Mg. The reformed vesicles bind Pfr in vitro. Pfr binding increases with decreasing pH and decreases with increasing monovalent cation concentration. Pfr is released from the membrane by far red light (Pr is formed) and by Triton X-100. We suggest that Pfr binding to a membrane induces conformational changes; the functional properties of this membrane are altered, which might lead to the observed phytochrome-mediated responses.
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  • 65
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    Journal of Supramolecular Structure 2 (1974), S. 715-727 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The nitrate reductase of E. coli is an inducible membrane protein with a molecular weight of about 800,000. The enzyme consists of four subunits of 60,000 molecular weight, four subunits of 142,000 molecular weight, four molecules of molybdenum, and nonheme iron. The enzyme may be solubilized by heat extraction, which results from limited digestion by a membrane-bound protease, or by Triton X-1 00. When the enzyme is isolated from Triton-solubilized cytoplasmic membrane by immune precipitation, it contains a third protein of 20,000 molecular weight which may be a cytochrome.Chlorate resistant (chl) mutants of E. coli lack functional nitrate reductase. Mutants of the classes (chl)and chlB have all of the enzyme polypeptides present in the membrane JI intact form, while in classes chlC and chlE the membrane contains degraded fragments of the polypeptides, suggesting proteolysis of a defective enzyme. Reconstitution of nitrate reductase activity occurs when soluble extracts of various classes of mutants are mixed and incubated at 32°C. This reconstitution requires three things: (a) intact enzyme polypeptides in the form of small soluble lipoprotein fragments resulting from fragmentation of the cytoplasmic membrane during cell breakage; (b) a molybdenum factor which is present in the wild-type membrane and which accumulates in the cytoplasm of chlB mutants in soluble form; and (c) a soluble factor or enzyme, presumably the chlB gene product, which adds the molybdenum factor to the enzymeTwo conclusions may be drawn from these observations. First, the enzyme is bound t o the membrane by small, hydrophobic regions on one or more of the subunits. Second, the process of reconstitution from mutant extracts is different from the process involved in de novo synthesis of the enzyme in wild-type E. coli.
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  • 66
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    Journal of Supramolecular Structure 2 (1974), S. 769-774 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Halobacterium halobium carries out photophosphorylation. A rhodopsin-like protein, bacteriorhodopsin, located in the cell membrane mediates the first step in energy transduction, the conversion of light energy into a chemiosmotic gradient. After absorption of a photon, bacteriorhodopsin undergoes a series of fast reactions, returning to its original state in a few milliseconds. In continuous light it cycles continuously at 100 to 200 cps. During a cycle protons are taken up on the cytoplasmic side of the membrane and released on the outer surface, thus generating a chemiosmotic gradient which can drive phosphorylation of ADP to ATP.
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  • 67
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    Journal of Supramolecular Structure 2 (1974), S. 775-780 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Living organisms use light as a source of energy and as a source of information. They have developed highly specialized photoenergy and photosignal transducing devices which serve these functions. Membranes are essential parts of both photosignal and photoenergy transducing systems.In photoenergy transduction a substantial part of the absorbed energy is conserved for times very long compared to the lifetime of excited states and converted finally to chemical free energy of ATP and other forms in which it can be stored for further use by the organism. In photosignal transduction light typically triggers an event which dissipates much more energy than is absorbed in the form of light. The additional energy had been stored previously by the organism through some energy transducing systems.
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  • 68
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    Journal of Supramolecular Structure 2 (1974), S. 1-6 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Previous work has suggested the presence of galactosyltransferases on the outer surface of the plasma membrane of a malignant and a nonmalignant cell line. This paper summarizes data indicating that three other classes of glycosyltransfeases are similarly located on cell surfaces. In addition to the original two cell lines examined, BALB/c 3T3 and BALB/c 3T12, two other lines of BALB/c origin have been investigated. These are the SV40-transformed 3T3 line and one of the revertants of the virally infected cells that is no longer malignant but retains a viral genome.
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  • 69
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    Journal of Supramolecular Structure 2 (1974), S. 7-16 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: As the size of rod membrane fragments was reduced by sonication or by addition of the detergent Emulphogene, the intensity of the circular dichroism (CD) bands (210 and 221 nm) increased progressively with a blue shift in position. The intensity of the visible CD bands (340 and 495 nm) was also increased by sonication. Since the intensity increase of the CD bands was related to a reduction in turbidity, the anomalous CD features of intact membranes could be attributed to optical artifacts caused by the particulate nature of the material.Because the magnitude of the CD bands at 221 nm and 340 nm was essentially identical for the sonic suspension and detergent-clarified solution, the adequacy of sonic suspensions can be assured by checking whether detergent affects the intensity of these bands.Suspensions of sonicated rod membranes, purified on Agarose, contained vesicles of 112 nm in average diameter. The morphology and size of the vesicles did not change upon photobleaching of rhodopsin. The vesicles retained such rod membrane properties as conformational insensitivity to photobleaching of the retinal chromophore, thermal stability, and pigment regenerability. Thus, the physiological integrity of rod membranes was maintained by the sonicated vesicles.From the most reliable estimate of the molecular ellipticity at 221 nm, the helical content of membrane-bound rhodopsin was determined to be approximately 47%.
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  • 70
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    Journal of Supramolecular Structure 2 (1974), S. 71-78 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Bilayers of human erythrocyte apoprotein-lipid complexes were made by dipping a mica plate through monolayers of the complex formed at the air-water interface. Stearic acid and erythrocyte lipid alone served as controls. Freeze-fracture images of the complex at high lipid surface pressures (30 dynes/cm) showed particles (average diameter, 109 Å ± 18 Å) similar to those of erythrocyte ghosts (average diameter, 102 Å ± 19 Å). Control surfaces were smooth. We conclude that part or all of the protein molecule penetrated into the lipid bilayer and that erythrocyte apoprotein-lipid complexes yield fracture faces similar to the native erythrocyte membrane.
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  • 71
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    Journal of Supramolecular Structure 2 (1974), S. 202-224 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: About 250 molecules of the 42,000 molecular weight gene 8 product catalyze the polymerization of the major phage coat protein into a precursor shell temporarily containing both proteins. The resulting prohead appears to be a shell structure with the P8, or scaffolding protein, on the inside, and the coat protein on the outside. In concert with DNA condensation inside the shell, all 250 scaffolding molecules exit from the prohead, without proteolytic cleavage. These molecules then recycle and catalyze the formation of more proheads from newly synthesized coat protein. Such proteins, which catalyze assembly by temporarily associating with an intermediate stage, may represent a general mechanism of macromolecular assembly.
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  • 72
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    Journal of Supramolecular Structure 2 (1974), S. 196-201 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Bacteriophage T4 tail fibers are rodlike structures with a contour length of about 1400 Å, a diameter of about 45 Å, and a total mass of about 600,000 daltons. The assembly of the tail fibers and their subsequent attachment to the phage particle are under the control of 8 phage-induced proteins. The gene control and molecular weight of each protein are known. The sequence of gene-controlled steps has been determined by the characterization of intermediates that accumulate when various steps are blocked by mutation. The protein composition of the fibers and their precursors has been determined by purification and electrophoretic analysis.Four of the eight gene products are structural components of the tail fiber. These proteins are P34 (150,000 daltons, 2 copies), P37 (120,000 daltons, 2 copies), P35 (40,000 daltons, 1 copy), and P36 (24,000 daltons, 2 copies). The wac (whisker antigen control) gene product is a structural component of the phage whiskers. The remaining three gene products, P38, P57, and P63, are not structural components of the phage particle. Both P63 and the wac gene product promote the attachment of tail fibers to the phage particle. P63 has been shown to act catalytically. Both P38 and P57 are somehow involved in the folding of the major tail fiber structural proteins (P37 and P34). The normal requirement for P38 and P57 functions can be bypassed by secondary mutations.
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  • 73
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    Journal of Supramolecular Structure 2 (1974), S. 737-750 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have developed methods for the isolation of Golgi apparatus from a number of mammalian tissues. The Golgi is distinct both chemically and enzymatically from the other membranes of the cell. For both liver and kidney, galactosyltransferase has been found to be a useful marker enzyme for Golgi membranes. This enzyme is involved in the modification of glycoproteins during secretion. In addition to lipoproteins and glycoproteins, the Golgi apparatus of liver is involved in the secretion of albumin, a simple protein. It does not, however, take part in the synthesis of sphingomyelin, lecithin, or triglycerides which are present in the secreted lipoproteins. These lipids appear to be synthesized predominantly by the endoplasmic reticulum. In kidney, which is rich in glycolipids, 3′-phosphoadenosine 5′-phosphosulfate, an enzyme which converts cerebroside to sulfatide, is localized predominantly in the Golgi apparatus. Thus, Golgi functions to modify glycolipids as well as mucopolysaccharides and proteins. Sulfatide constitutes a significant fraction of the total lipid of both Golgi and plasma membranes of kidney. When 35S-sulfate is injected into rats, it is incorporated first into the sulfatides of the Golgi apparatus and later appears in the sulfatides of the plasma membrane. The data are consistent with the view that sulfatides are formed in the Golgi apparatus of kidney and then transported to the plasma membrane.
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  • 74
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    Journal of Supramolecular Structure 2 (1974), S. 385-392 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 5 Ill.
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  • 75
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    Journal of Supramolecular Structure 2 (1974), S. 486-495 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Structural studies of tomato bushy stunt virus and Sindbis virus are discussed in terms of the information they provide about specificity and control in virus and membrane assembly.
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  • 76
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    Journal of Supramolecular Structure 2 (1974) 
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    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 77
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    Journal of Supramolecular Structure 2 (1974), S. 529-537 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 78
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    Journal of Supramolecular Structure 2 (1974), S. 593-608 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: ESR analysis of membranes from cultured animal cells reveals a more complex lipid phase behavior than that displayed by ideal binary lipid systems. When endoplasmic reticulum membranes from LM cells are spin labeled with a nitroxide derivative of decane, 5N10, and scanned by ESR at 1° C-intervals, the partitioning of 5N10 between the hydrocarbon and aqueous portions of the membrane suspension undergoes thermotropic changes at characteristic temperatures of 9°, 16°, 22°, 32°, and 38° C. Lipids extracted from these same membranes, however, exhibit only two characteristic temperatures, 16° and 35° C, and in this respect resemble binary lipid systems. The phase behavior of lipids in animal cell membranes is suggestive of an organized distribution of lipid which is disrupted by extraction. In support of this, mathematical treatment of the partitioning data indicates that four of these characteristic temperatures can define the boundaries (i.e., the t1 and th ) of two independent phase transitions in endoplasmic reticulum membranes. These results are similar to those of a physical treatment of data from plasma membranes of both mouse and chick cells in which the two monolayers appear to exist as independent physical entities with different physical properties. The most probable phase boundaries for the two monolayers of the endoplasmic reticulum membranes studied here are 16° and 32° C for one monolayer and 22° and 38° C for the other.
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    Journal of Supramolecular Structure 2 (1974), S. 617-628 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The physical state of the membrane lipids, as determined by fatty acid composition and environmental temperature, has a marked effect both on the temperature range within which A. laidlawii can grow and on the temperature coefficient of growth within the permissible temperature range. The minimum growth temperature under certain conditions is clearly defined by the lower boundary of the gel-to-liquid-crystalline phase transition of the membrane lipids. The physical state of the membrane lipids can also influence the optimum and maximum growth temperatures. An a brupt increase in the temperature coefficient of growth is noted at temperatures between the phase transition boundaries. Both the absolute rates and the temperature coefficients of cell growth are similar for cells whose membrane lipids exist entirely or predominantly in the liquid-crystalline state, but absolute growth rates decline rapidly and temperature coefficients increase when most of the membrane lipids become solidified. Some cell growth, however, can continue at temperatures at which less than 10% of the total lipid remains in the fluid state. Conversion of the membrane lipid from the liquid-crystalline to the gel state is accompanied by a progressive aggregation of intramembranous protein particles. An appreciable heterogeneity in the physical state of the membrane lipids can apparently be tolerated by this organism without a detectable loss of membrane function.
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  • 80
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 629-645 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Concanavalin A (Con A) binding and Con A-mediated hemadsorption to LM cells were found to decrease significantly at both 5-7°C and 15-19°C. The higher of these critical temperatures responds to a change in state of the membrane lipids and can be increased or decreased in cells where the membrane phospholipids contain less or more double bonds, respectively. The lower critical temperature for Con A binding or Con A-mediated hemadsorption does not respond to these changes in membrane lipid composition. Though the amount of Con A bound to the cell surface is a determinant of Con A-mediated agglutinability, the major components of the decreases in Con A-mediated hemadsorption which occur at both these critical temperatures do not have their origin in the decreases in Con A binding which occur over these same temperature ranges - that is 5-7°C and 15-19°C.Con A-mediated hemadsorption measured at 22°C was dramatically inhibited when LM cells were first incubated at 7°C or less. Reversal of this inhibition required 20-30 min of subsequent incubation at 22°C, indicating that factors other than membrane lipid “fluidity” are determinants of agglutinability. LM cells treated with the microtubule-disrupting alkaloids colchicine, colcemid, or vinblastine at concentrations as low as 10-6 M were as much as fourfold more agglutinable with Con A. By contrast, lumicolchicine, an inactive derivative of colchicine, had a slight inhibitory effect on Con A-mediated hemadsorption. Colchicine, vinblastine, or lumicolchicine treatment of LM cells did not alter the quantitative binding of labeled lectin. The results suggest that membrane lipid “fluidity” and the cell cytoskeleton (microtubule/microfilament system) are important determinants of lectin interactions with cell surfaces. The results are interpreted in terms of a model of cell-cell and cell-lectin interactions which assigns a central role to the Con A receptor.
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  • 81
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    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 2 (1974), S. 695-714 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Additional Material: 15 Ill.
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  • 82
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    Journal of Supramolecular Structure 2 (1974), S. 682-694 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Physical studies on the formation and structure of mixed micelles of the nonionic surfactant Triton X-100 and phospholipids and enzymatic studies on the action of phospholipase A2 toward these mixed micelles are presented. Results of nmr intensity, line width, and T1 determinations, as well as gel chromatography and centrifugation experiments on the interaction of Triton X-100 with egg and dipalmitoyl phosphatidylcholine, are presented and discussed. The structure of mixed micelles is discussed in terms of a working schematic model which is consistent with the experimental results. Kinetic studies on phospholipase A2 (Naja naja) action are then analyzed in terms of this model. The temperature dependence of phospholipase A2 action toward dipalmitoyl phosphatidylcholine is considered in terms of the effect of thermotropic phase transitions on mixed micelle formation. The phospholipase A2-dipalmitoyl phosphatidylcholine-Triton X-100 system is then considered as an artificial model system for studying the effect of lipid phase separations on biological activity.
    Additional Material: 6 Ill.
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  • 83
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    Journal of Supramolecular Structure 2 (1974), S. 349-359 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: groE bacterial mutants of E. coli have been isolated on the basis of their inability to propagate bacteriophage λ. The block exerted on λ growth has been shown to operate at the level of head assembly. Some groE mutations express pleiotropic effects, such as inability to propagate T4 and T5 or inability to form colonies at high temperature. P1 transduction experiments show that these groE mutations map at 83 min on the genetic map of E. coli and that a single mutation is responsible for the pleiotropic effects observed. At 43°C, some of the groE strains are temperature sensitive for growth and form long filamentous structures. Examination of the proteins synthesized at 43° by one of the temperature-sensitive groE strains, groEA44, by SDS gel electrophoresis reveals a pattern of synthesis somewhat different from that exhibited by the gro+ parent strain: some new bands appear, while others disappear.
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  • 84
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    Journal of Supramolecular Structure 2 (1974), S. 337-348 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Satellite phage P4 causes the head proteins of a helper phage, such as P2, to form a small head. This small head is never found in cells infected by the helper virus alone. This finding, coupled with the dominance of P4 over its helper, indicates that the P4 genome has the potential for specific head size determination. Satellite phage P4 codes for a late protein which is found in the P4 head (45 copies/head). This protein may determine head size. Our finding that the small size of P4 DNA does not determine small head size in an in vitro DNA packaging system lends further support to the idea that a P4 protein determines small head size.Formation of P2 headlike structures is accompanied by cleavage of P2 head proteins. Cleavage of the major head protein precursor can be observed in vitro after lysis of infected cells with lysozyme. The rate of this in vitro reaction is not affected by deoxyribonuclease; thus there cannot be a tight coupling between DNA packaging and the cleavage of the major capsid protein.
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  • 85
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    Journal of Supramolecular Structure 2 (1974), S. 466-485 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Long chain glycols augment in size and birefringence the in vivo mitotic apparatus (MA) of marine eggs. Dinitrophenol and caffeine antagonize the effect but they can be balanced by glycols. Caffeine inhibits the phosphodiesterase for cyclic AMP (CAMP) and CAMP levels increase in its presence. However, added dibutyryl CAMP does not affect MAs or cleavage, but is taken up by eggs. Oxygen uptake studies show that caffeine depresses oxidative metabolism but does not affect ATP levels. Action through the pentosephosphate shunt is suggested.Glycols influence the assembly of tubulin. Optical ultracentrifuge patterns of tubulin polymerized without glycol show a 6S and 30S peak. Similar patterns of tubulin polymerized at pH 6.4 in glycol and depolymerized in its absence show 6S, 8-18S, and 30S, peaks. The 8-18S peak appears in equilibrium with the 6S peak. If glycol is added to cold tubulin polymerized without glycol, only 6S and 30S peaks occur. Preparations with no 30S peak do not show 450 Å rings in the EM. Calcium depolymerizes microtubules. In the absence of glycols 450 Å rings are seen. In the presence of glycol, much higher concentrations of calcium are necessary for depolymerization, and few 450 Å rings occur.We suggest that glycols prevent formation of the stable 30S peak, favor an intermediate structure in equilibrium with the 6S peak, and antagonize calcium depolymerization. Their in vivo effects may arise from these interactions.
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  • 86
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    Journal of Supramolecular Structure 2 (1974), S. 79-80 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 87
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    Journal of Supramolecular Structure 2 (1974), S. 99-102 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The structure and self-assembly of collagen and procollagen molecules are reviewed. The registration peptides of procollagen have specific recognition properties which assure (1) selection of component polypeptide chains and (2) registration of their N-termini, facilitating orderly folding into a collagen helix. The stability of this helix relative to body temperature is critically altered by post-ribosomal hydroxylation of proline residues. The registration peptides of procollagen may have additional functions such as preventing intracellular fiber formation.
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  • 88
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The three-dimensional structure of the multisubunit allosteric enzyme, aspartate transcarbamylase, has been determined to 5.5 Å resolution. An unusual feature of the molecule is a large central aqueous cavity 50 Å × 50 Å × 25 Å, into which the active sites face. Access to the central cavity and the active site region is provided by six equivalent channels of 15 Å diameter.A complex C6R4, composed of catalytic trimers C3 and of regulatory dimers R2, has been isolated upon treatment of aspartate transcarbamylase (ATCase, C6R6) by mercurials. The specific catalytic activity of C6R4 is essentially the same as that of ATCase, about 70% of that of the catalytic trimers at 30 mM aspartate and saturating carbamyl phosphate. Allosteric interactions are reduced in C6R4 as compared with those in ATCase. In the homotropic interactions the Hill coefficient is reduced from approximately 3.3 to 2.1 at pH 8.3, while the heterotropic interactions of both cytidine triphosphate (CTP) and adenosine triphosphate (ATP) are reduced substantially but not abolished at pH 8.3. Thus, the allosteric transitions involved in the regulatory mechanisms do not require the intact structure C6R6. Also, this regulation is not simply the control of access of substrates or products to or from the large central aqueous cavity in the ATCase molecule.Comparison of electron density maps at 5.5 Å resolution for ATCase and for the complex of ATCase with CTP shows substantial similarities throughout the three-dimensional electron density maps. Significant differences are seen, however, in the region of the regulatory dimers R2 where CTP adds, and near the active sites in the catalytic trimers C3.
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  • 89
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    Journal of Supramolecular Structure 2 (1974), S. 360-371 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The basal structure of the flagellum controls both activity and assembly. In order to define the steps involved in these processes, genetic analysis was performed. Twenty genes were found to be required for the complete assembly and function of the organelle. FlaE controls the length of the hook, flaA is required both to maintain flagellar structure and for chemotaxis, and flaI plays a role in regulating the synthesis of the entire structure. Mutations mapping close to flal (the cfs mutations) release flagellar synthesis from control by catabolite repression.The basal structure was purified and isolated. On SDS acrylamide gel electrophoresis, it contained at least six distinguishable components. One major band corresponded to the hook subunit with an apparent molecular weight of 42,000 daltons. The others had apparent molecular weights of 60,000, 40,000, 28,000, 25,000, and 18,000 daltons. The genes that correspond to these polypeptides have not been identified.In exploring the role of the mot and che genes, assays were developed for the function of individual flagellar filaments. The filaments were found to rotate and rotation could be modulated by changing their direction. Chemotaxis results from the modulation of flagellar rotation. Using the rotation assay the response of nonmotile cells to attractants and repellents was followed.
    Additional Material: 6 Ill.
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  • 90
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    Journal of Supramolecular Structure 2 (1974), S. 412-428 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The mechanism of microtubule polymerization and depolymerization has been studied with protein purified from extracts of porcine brain. Under polymerizing conditions characteristic microtubules composed of parallel protofilaments are observed in the electron microscope. Under depolymerizing conditions three forms are observed: double rings of outside diameter 49 nm, spirals, and 7-nm globular subunits. Under the same conditions two boundaries are observed in the analytical ultracentrifuge at 6S and 36S, whether depolymerization is accomplished by cooling to 0°C, by addition of 1 mM CaCl2 at 25°C, or by removal of GTP. On polymerization all of the 36S and most of the 6S is converted to a fast-sedimenting form which the electron microscope reveals to be microtubules.The depolymerization mixture may be fractionated by gel chromatography into two fractions, one consisting solely of 6S and the other mostly 36S. Neither fraction regenerates the original equilibrium mixture. The 36S form may be reversibly dissociated into 6S subunits by addition of NaCl. From these and other considerations we have postulated that microtubule protein is composed of two different types of tubulin, both of which participate in polymerization. Studies are reported showing that colchicine does not dissociate microtubule rings but blocks polymerization by interfering with their proper lateral association into a protofilament array within microtubules. The role of GTP in polymerization is also discussed. Electron micrographic evidence is presented suggesting the conversion of protofilaments directly into rings and spirals, and a pathway for microtubule assembly is proposed.
    Additional Material: 12 Ill.
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  • 91
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    Journal of Supramolecular Structure 2 (1974), S. 517-528 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: A brief description of endocytosis and exocytosis is followed by a discussion of the experimental approaches to the study of the initial events of endocytosis, the possible involvement of microfilaments, and in particular the possible role of membrane lipids in the events of membrane fusion. Recently developed model systems are also discussed.
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  • 92
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    Journal of Supramolecular Structure 2 (1974), S. 582-592 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The acetylcholine receptor from Torpedo californica electroplax has been studied at three levels of molecular organization: receptor-rich membrane fragments, solubilized and purified receptor, and reconstituted receptor in phospholipid vesicles. The binding of cholinergic ligands to the membrane-bound and the solubilized material is not cooperative, and the number of ligand sites is less than the number of toxin sites. In addition, the purified macromolecule contains the molecular features necessary for ion-translocation during postsynaptic depolarization, since a chemically excitable membrane can be formed from purified receptor and Torpedo phospholipids.
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  • 93
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    Journal of Supramolecular Structure 2 (1974), S. 609-616 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Lateral phase separations in lipid and lipid-protein systems are discussed with the aid of phase diagrams derived from spin-label measurements. Freeze-fracture data from E. coli membranes and model lipid-protein bilayers indicate that the protein tends to associate with fluid lipid phases.
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  • 94
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    Journal of Supramolecular Structure 2 (1974), S. 646-669 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Presently there is much interest in the relationship between the structure and function of biological membranes. An approach to the understanding of this relationship has been the study of the effect of the modification of the membrane lipids on the function of membrane-associated activities. In our laboratories we have modified the apolar portion of the membrane lipids of unsaturated fatty-acid auxotrophs of Escherichia coli and investigated the effect of such modifications on enzymes of the electron-transport system. From these studies we were able to conclude that E. coli regulates the relative fatty-acid content of its phospholipids and maintains a certain membrane fluidity necessary for proper membrane function (1-3). We have also proposed that lipids are heterogeneously distributed within the membrane in domains of differing fluidity (4). The studies of McConnell, Chapman, and others (5-13) have corroborated these concepts and extended them to other biological and model membranes. In this paper we review some of our previous results and present evidence to show how NADH and D-lactate oxidases of E. coli membranes are influenced by the fluid states of membrane phospholipids. Preliminary evidence is also presented to show that biogenesis of membranes probably occurs by independent insertion into the membranes of lipids and proteins which upon subsequent interaction with each other form the functional lipoprotein units.
    Additional Material: 13 Ill.
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  • 95
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    Journal of Supramolecular Structure 2 (1974), S. 17-31 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: From an analysis of electron micrographs of Alfalfa Mosaic Virus (AMV), evidence has been obtained which favors a cylindrical P6 lattice for the protein coat of the virus. For the analysis use was made of optical diffraction and computer processing of electron images of negatively stained virus particles.The virus coat exhibits polymorphism. Two kinds of structure were found: a stacked and a helical type. In the stacked type of lattice the unit cells are arranged in staggered rings in such a way that two rings comprise a repeat distance of the structure. The selection rule for the optical diffraction patterns of the stacked form is 1 = n + 2m, in which n is an integer multiple of 3. The layerlines are equally spaced at a distance of approximately 1/80 Å-1.In the helical type of lattice these rings of unit cells are transformed into turns of a double helix. The selection rule derived in this case is 1 = 6n - 17m, in which n is an integer multiple of 2. The repeat of the structure is approximately 440 Å.
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  • 96
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    Journal of Supramolecular Structure 2 (1974), S. 81-81 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
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  • 97
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    Journal of Supramolecular Structure 2 (1974), S. 512-514 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The status of research on macromolecular assembly is similar in several respects to that of research on macromolecular synthesis in the late 1950's. The work of that era can teach us some lessons, but it also has left us with some preconceptions that may be misleading us in our attempts to understand assembly mechanisms.
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  • 98
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    Journal of Supramolecular Structure 2 (1974), S. 538-557 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Alamethicin, monazomycin, or EIM induce electrical excitability in lipid bilayers. The voltage-dependent gating displays all the characteristics observed in excitable cells and its basic features can be quantitatively described by the Hodgkin-Huxley equations.A common molecular mechanism of membrane excitation has been postulated. It assumes that in the absence of an electrical field the channel-forming molecules lie at the surface of the membrane. An applied potential tilts them from the surface into the hydrocarbon region of the bilayer. Once in this position the molecules diffuse laterally and form aggregates which act as channels for the flow of ions.In the case of alamethicin we assume that the molecule forms an elongated ellipsoid with two glutamic residues at one end, and a metal ion in four- or five-fold coordination with peptide carbonyl oxygens at the other. An applied field pulls the cationic end through the membrane to the other side, while the glutamic residues hold the other end attached to the original surface. The molecules now span the membrane and aggregate, forming oligomeric channels in which most of the peptide carbonyls face toward the center, and the methyl groups outward.Monomers and dimers do not conduct and an individual channel can have different conductance values depending on the number of monomers in the aggregate and the resulting channel diameter. A quantitative description of this process matches observed gating kinetics, gating currents, and the single channel conductance increments. Without additional assumptions, inactivation follows directly from the aggregation process because with proper rate constants, the average degree of polymerization and therefore number of open channels goes through a maximum in time.The model may also apply to the excitation process of higher cells.
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  • 99
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    Journal of Supramolecular Structure 2 (1974), S. 558-581 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Internal dialysis techniques have been used to examine the influence of external and internal cations on Ca efflux from ATP-depleted squid axons. The main observation is that Ca efflux is promoted by external Na and inhibited by internal Na. The Na0 -dependent Ca efflux appears to be a function of [Na]03, and is also affected by the membrane potential; a 25 mV depolarization may cause as much as an e-fold decrease in Ca efflux. These data are consistent with a counter-transport exchange of 3Na+-for-1Ca2+. A Ca0-dependent Ca efflux has also been observed; it is prominent in Na sea water or Le sea water, and is markedly diminished in choline sea water. This flux is consistent with the idea of a Ca-Ca exchange diffusion process. Taken together, the Na0 - and the Ca0 -dependent Ca effluxes fit a two-site model for carrier-mediated Ca transport; one site binds two Na+ or one Ca2+, while the second site can bind either one Na+ or one Li+. The data reported here suggest that both sites must be filled on the inward journey, but that only the Ca-binding site need be occupied on the outward journey of the carrier. A mechanism of this type could derive sufficient energy from the Na and voltage gradients to maintain a [Ca2+]0/[Ca2+]i concentration ratio of about 104 in the absence of ATP. The present experiments do not, however, rule out the possible participation of a metabolically driven Ca transport mechanism in vivo.
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  • 100
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    Journal of Supramolecular Structure 2 (1974), S. 103-107 
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Disulfide-linked, triple-stranded procollagen (pro γ 112) was isolated from chick embryo skull bones. It was reversibly denatured and renatured as judged by sedimentation properties and susceptibility to digestion with pepsin. Refolding was an intramolecular process and aggregation between molecules did not occur.
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