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  • Chemistry  (3)
  • ACC synthase  (2)
  • DNA sequencing  (2)
  • Ordination  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Molecular & Biochemical Parasitology 59 (1993), S. 15-27 
    ISSN: 0166-6851
    Keywords: DNA sequencing ; HGPRTase ; Leishmania donovani ; OMP ; PCR ; PRPP ; PRS ; Phosphoribosylpyrophosphate ; Phosphoribosylpyrophosphate synthetase ; Purine metabolism ; Pyrimidine metabolism ; hypoxanthine-guanine phosphoribosyltransferase ; orotidylate ; phosphoribosylpyrophosphate ; phosphoribosylpyrophosphate synthetase ; polymerase chain reaction
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Molecular & Biochemical Parasitology 59 (1993), S. 15-27 
    ISSN: 0166-6851
    Keywords: DNA sequencing ; HGPRTase ; Leishmania donovani ; OMP ; PCR ; PRPP ; PRS ; Phosphoribosylpyrophosphate ; Phosphoribosylpyrophosphate synthetase ; Purine metabolism ; Pyrimidine metabolism ; hypoxanthine-guanine phosphoribosyltransferase ; orotidylate ; phosphoribosylpyrophosphate ; phosphoribosylpyrophosphate synthetase ; polymerase chain reaction
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-5028
    Keywords: 1-aminocyclopropane-1-carboxylic acid (ACC) ; ACC synthase ; S-adenosylmethionine (AdoMet) ; ethylene ; polymerase chain reaction (PCR) ; Vigna radiata
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The polymerase chain reaction (PCR) was used to produce 3 putative clones for ACC synthase from etiolated mung bean (Vigna radiata Rwilcz cv. Berken) hypocotyls. This was accomplished by utilizing genomic DNA from mung bean and degenerate primers made from information derived from highly conserved regions of ACC synthase from different plant tissues. The total length of pMAC-1, pMAC-2 and pMAC-3 are 308, 321, and 326 bp, respectively, all of which code for 68 amino acids. The introns for pMAC-1, pMAC-2 and pMAC-3 are 92, 105, and 110 bp, respectively. The degrees of homology at the DNA level for each of these clones is ca. 80% in their coding region and ca. 50% in their respective introns. This is the first report providing evidence that there are at least 3 genes for ACC synthase in etiolated mung bean.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-5028
    Keywords: 1-aminocyclopropane-1-carboxylic acid (ACC) ; ACC synthase ; indole-3-acetic acid (IAA) ; ethylene ; Vigna radiata
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 1-Aminocyclopropane-1-carboxylate (ACC) synthase (EC 4.4.1.14) is the key regulatory enzyme in the ethylene biosynthetic pathway. The identification and characterization of a full-length cDNA (pAIM-1) 1941 bp in length for indole-3-acetic acid (IAA)-induced ACC synthase is described in this paper. The pAIM-1 clone has an 87 bp leader and a 402 bp trailing sequence. The open reading frame is 1452 bp long encoding for a 54.6 kDa polypeptide (484 amino acids) which has a calculated isoelectric point of 6.0. In vitro transcription and translation experiments support the calculated molecular weight and show that the enzyme does not undergo processing. Eleven of the twelve amino acid residues which are conserved in aminotransferases are found in pAIM-1. The sequence for pMAC-1 which is one of the 5 genes we have identified in mung bean is contained in pAIM-1. pAIM-1 shares between 52 to 65% homology with previously reported sequences for ACC synthase at the protein level. There is little detectable pAIM-1 message found in untreated mung bean tissues; however, expression is apparent within 30 min following the addition of 10 μM IAA reaching a peak after approximately 5 h with a slight decrease in message after 12 h. These changes in message correlate with changes in ACC levels found in these tissues following treatment with 10 μM IAA.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 13 (1990), S. 567-569 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Mass spectrometry ; Oxazaphosphorines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 29 (1987), S. 176-179 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Eight chemically modified cellulose supports were tested for their ability to absorb components of the Aspergillus niger cellulase system. At least two of the most effective adsorbents, aminoethyl cellulose and carboxymethyl cellulose, were shown to be useful for the fractionation of cellulases. These supports apparently owe their resolving capacity to both ion exchange and biospecific binding effects; however, the relative importance of each effect is unknown. These observations form the basis for a new cellulase fractionation technique, combined ion exchange-affinity chromatography.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Plant ecology 51 (1983), S. 141-155 
    ISSN: 1573-5052
    Keywords: Correlation matrix ; Dispersion matrix ; Forest model ; Hierarchical structure ; Ordination ; Principal components analysis ; Simulation ; Succession
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A model of a 1/12th ha forest stand, FORET, generated 10 000 years of simulated species succession. Approximately the first third of these results were analyzed by principal component analysis as if they were collected field data to give the trajectory of the community particle in a collapsed species space. The ordination axis orientation was performed on a dispersion matrix and correlation matrix between species. In both cases, however, the eigen vectors were applied to the data matrix which had not been transformed to unit species variance. This facilitated comparison of species dispersion and correlation structure; it emerged they were very different. Correlation structure gave large weights to understory species while dispersion emphasized the dominant overstory species. This implies a decomposition of simulated stand behavior into overstory and understory, even though such decomposition was not formally built into the model. This decomposition would seem to pertain to real vegetation. Principal component analysis was able to express insightful differences between data structure with and without the unit variance transformation implicit in the correlation matrix. This flexibility of the ordination method proved valuable in uncovering unsuspected ordering principles in the model. Complex simulated data allow the ordination technique to demonstrate its capacity to generate new hypotheses, which hypotheses can then be simply validated by a return to the structure of the model but with the hindsight of the analysis. The generation of new hypotheses is not possible if the simulation is of a simple coenocline; on the other hand, ordination of test field data does not allow the simple validation of new hypotheses, for in the field there is not a defined algorithm to which the researcher can return.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Plant ecology 56 (1984), S. 147-160 
    ISSN: 1573-5052
    Keywords: Data transformation ; Ordination ; Phytoplankton ; Principal components analysis ; Scale
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Data transformation is seen here as an aspect of scaling such that we are less interested in the quirks and properties of each transformation but are more concerned with the general scaling properties and trends of suites of transformations. Over two years of daily phytoplankton abundance data for 30 species from a temperate lake (Llyn Maelog, North Wales) were subjected to a series of scale-ordered transformations. Two major classes of transformation were systematically varied: binary and smoothing. Binary transformation scaled the cutoff threshold between ‘presence’ and ‘absence’ of a species to various levels of abundance. With successively smaller universes and smoothing windows and successive species exclusion, ordinations of sample dates revealed smaller scaled structures in the order: annual cycles of species turnover, seasonal areas of attraction and uniqueness of individual sample dates. Gradual increases in the length of the smoothing window resulted in gradual shifts in the positions of points in sample data ordination, but not necessarily in the species ordinations. Thus sample data structures are more stable with change in scale than are species data structures. These differences in stability are discussed in the context of filtering characteristics of data collection and data analysis. Transformations producing similar species statistics (means, variances and skews) did not generally give similar ordination results, while some transformations giving similar ordinations differed in species statistical parameters.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fidelity achieved in first derivative profiles of DNA thermal denaturation is shown to depend on a number of factors including the thermal increment of data gathering, the precision of absorbance readings, and the manner in which data are smoothed prior to calculating the derivative of hyperchromicity. The closeness with which thermal denaturation data can be fitted by a cubic polynomial is carefully considered, and a derivation is presented for the estimated error in calculated values of the derivative of hyperchromicity with respect to temperature. After reviewing both theoretical and experimental evidence for the expected minimum width of a thermal transition in DNA, we conclude that thermal increments of 0.05°C or less are required for an adequate representation of transitions in naturally occurring DNA's.Data gathered under conditions meeting the requirements suggested here for quantitative recording of thermal denaturation profiles (Vizard and Ansevin, submitted for publication) show that virtually all of the high-resolution thermal denaturation profile of a simple, naturally occuring DNA may consist of small subtransitions, which we call thermalites. The finding of substransitions is consistent with current theories of DNA melting. A particularly well-resolved thermalite of λ bacteriophage DNA has a breadth of only 0.30°C (2σ width), and thus is narrower than previously reported thermal transitions for DNA. For this thermalite, the combination of width, shape, and position in the profile suggests that the substransitions observed in accurately recorded DNA thermal denaturation profiles are not described satisfactorily by existing theories.Knowledge of the requirements for the quantitative recording of thermal denaturation profiles should greatly favor the usefulness of denaturation experiments for physical genomic analysis.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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