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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für Lebensmittel-Untersuchung und -Forschung 206 (1998), S. 323-328 
    ISSN: 1431-4630
    Keywords: Key words Collagen ; D-Amino acids ; Hydroxyproline stereoisomers ; Racemisation ; Food proteins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract  Using capillary gas chromatography on chiral stationary phases total hydrolysates of gelatins were investigated for their amounts of D-amino acids (D-AAs). Gelatins of different quality and origin were analysed including gelatin-containing final products like candies and meat products. In gelatins manufactured by stepwise extraction (first to fifth extract) with water of increasing temperature (ca. 55–95°C) amounts of 2.7–4.8% of D-aspartic acid (D-Asp) were determined in extracts obtained at ≤ 85°C. The amounts D-Asp were as high as 28.1% in fifth extracts obtained at 95°C (data corrected for 4.3% of D-Asp determined in native collagen as a result of acid-induced epimerisation of L-Asp during total hydrolysis). Epimerisation of aspartyl or asparaginyl residues of proteins in general on heating in water is assumed to proceed via formation of aspartyl succinimide, tautomerisation and release of D-Asp on total hydrolysis. The other AA residues of gelatin showed only a slight increase of epimerisation with increasing thermal treatment. Furthermore, amounts of 3–4% of cis-4-D-hydroxyproline, formed from native trans-4-L-hydroxyproline in collagen on hydrolysis, were detected in total hydrolysates of all gelatins.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für Lebensmittel-Untersuchung und -Forschung 207 (1998), S. 400-409 
    ISSN: 1431-4630
    Keywords: Key words d-Amino acids ; Chemical markers ; Acetic fermentation ; Aceto balsamico ; Authenticity control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract  Twenty-five vinegars were examined quantitatively for their content of free amino acid (AA) enantiomers using chiral gas chromatography/mass spectrometry. Vinegars manufactured from grape must contained l-proline (l-Pro) as the major AA. Balsamic vinegars (aceto balsamico di Modena), with one exception, contained the highest amounts of l-AAs (861–2000 mg l–1) as well as d-AAs (46–361 mg l–1). The amounts of d-Pro and d-alanine (d-Ala) increased in the course of maturation. Sherry vinegars had a AA pattern similar to that of balsamic vinegars but with much lower amounts: concentrations of l-AAs were 244 mg l–1 and 456 mg l–1 and of d-AAs were 18 mg l–1 and 19 mg l–1. The l-AA content of cider vinegars was very low (34 mg l–1 and 44 mg l–1) and only traces of d-AAs (〈2 mg l–1) were found. In spirit vinegars few d-AAs and low amounts of most l-AAs were detected, with the exception of l-glutamic acid (l-Glu) (210–847 mg l–1), probably added as a flavour enhancer. The AA content of spirit vinegars blended with wine vinegar was influenced by the portion of wine vinegar added. Rice vinegars had concentrations of l-AAs from as low as 36 mg l–1 to as high as 6860 mg l–1, and the concentrations of d-AAs ranged from 6 mg l–1 to 531 mg l–1. All vinegars declared as "produced by microbial fermentation" contained d-Ala, d-aspartic acid, and d-Glu as typical bacterial markers. From the data it is concluded that chiral AA analysis can be used to distinguish among fermented and synthetic vinegars and to identify raw materials used for their production. In particular, the amount of d-Pro can be used as proof of the maturation process of balsamic vinegar.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für Lebensmittel-Untersuchung und -Forschung 208 (1999), S. 424-428 
    ISSN: 1431-4630
    Keywords: Key words Amino acid epimerization ; Infant formulae ; Food proteins ; Hydroxyproline stereoisomers ; Gas chromatography-mass spectrometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract  Aqueous solutions (5 g/100 ml) of commercial preparations of (a) an enzymatic partial hydrolysate of gelatin and (b) type A gelatin were subjected to threefold heating to boiling in a domestic microwave oven at 750 W and to conventional heating. Then samples were totally hydrolyzed (6 M hydrochloric acid, 110  °C, 24 h) and investigated for the presence of eight possible stereoisomers of 3- and 4-hydroxyproline (Hyp) using capillary gas chromatography. Amino acids were analyzed as N(O)-trifluoroacetyl 2-propyl esters on Chirasil-l-Val and detected by selected ion monitoring mass spectrometry. Blanks of (a) and (b) were analyzed in parallel. Relative amounts of 5.0±0.2% cis-4-d-Hyp were generated from native trans-4-l-Hyp as a result of total hydrolysis in all samples and independent of previous treatment. Notably, neither cis-3-l-Hyp nor cis-4-l-Hyp could be detected in either of the gelatin samples. Thus a report on the generation of antifibrotic and therefore potentially hazardous cis-3-l-Hyp and cis-4-l-Hyp from protein-bonded native trans-3-l-Hyp and trans-4-l-Hyp on microwave heating of infant formulae could not be confirmed.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1420-9071
    Keywords: Trichoderma reesei ; molds ; paracelsin ; 13C NMR spectroscopy ; circular dichroism ; antibiotics ; polypeptide ; mycotoxins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Paracelsin, a hemolytic and membrane active polypeptide antibiotic of the peptaibol class which is excreted by the moldTrichderma reesei, was obtained by a simplified and isolation procedure utilziing hydrophobic adsorber resin. Investigation by13C nuclear magnetic resonance spectroscopy and circular dichroism revealed considerable helical portions in solution, and the very recently accomplished sequence determination of paracelsin allows the discussion of the results with regard to the closely related analogues, alamethicin and suzukacillin. A selective cleavage of the peptide was achieved by careful treatment with various acids, and a buffer of pH 8.25 and of high ionic strength made possible the quantitative determination of the C-terminal phenylalaninol released by means of ion-exchange chromatography. The significance of the production of paracelsin and related mycotoxins of the peptaibol class, exhibiting various kinds of biological activity, is discussed with respect to the extensive effort being made towards biotechnological applications of species, strains and cellulolytically highly active mutants of the fungusTrichoderma.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 174 (1991), S. 878-884 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    Journal of metamorphic geology 14 (1996), S. 0 
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Ion probe traverses across garnets from peridotites of the Caledonides of Norway and the Variscides of Poland show zoning patterns for Y, V, Zr, Cr, Ti and the REE. The complexly zoned patterns of garnets from the Bystrzyca Górna peridotite, Poland, are interpreted in terms of a changing P–T history (isobaric cooling followed by decompression and cooling). Weak rimward gradients in REE concentrations in garnets from the Almklovdalen and Sandvika peridotites, Norway, may be relicts of the original growth history of the garnets, but the nearly flat Y, V, Zr, Cr and Ti profiles from the same garnets imply a later period of near-homogenization at uniform P–T. Crushed garnet separates from each body were separated into three or more fractions on the assumption that density and magnetic susceptibility vary with Fe/Mg ratio, and Fe/Mg ratios change from garnet core to rim. Sm-Nd garnet–clinopyroxene ‘ages’ were determined for each fraction to determine whether they are also zoned. Four garnet fractions from the Góry Sowie peridotite give nearly the same ages (397–412 Ma) that are believed to span the interval of garnet growth. Garnet fractions from the Norwegian peridotites define scattered ages (816–1350 Ma) that are suspect, but hint at a Sveconorwegian equilibration event. The data indicate the Variscan and Norwegian peridotites had different histories, despite superficial mineralogical and tectonic similarities. Norwegian garnet peridotites had a long pre-Caledonian history and were extracted from a relatively cold mantle whereas the Variscan garnet peridotites had a comparatively short pre- or Eo-Variscan history and were extracted from a hot mantle.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: New petrographic evidence and a review of the latest radiometric age data are taken to indicate that formation of the ultra-high pressure (UHP) eclogites within the Western Gneiss Region of Norway probably occurred within the 400–410 Ma time frame. Thus, this event took place significantly later than the previous, widely accepted age of c. 425 Ma for the timing of the high pressure metamorphism in this part of the Scandinavian Caledonides. Garnet growth under UHP (coesite-stable) conditions is recognised as a discrete, younger event following on from earlier garnet formed under firstly amphibolite facies then quartz-stable, eclogite facies conditions. Currently, the best constrained and most precise age, specifically for UHP mineral growth, is the 402 ± 2 Ma U–Pb age for metamorphic zircon (some of which retain coesite inclusions) from the Hareidland eclogite. Exhumation must have followed shortly thereafter and, based on synoptic pressure–temperature and depth–time curves, must have been very fast. Our data and those of others indicate an initial fast exhumation to about 35 km depth by about 395 Ma at a mean rate of about 10 mm a−1. This rapid exhumation rate may have been driven by the appreciable residual buoyancy of the deeply subducted continental crustal slab due to incomplete eclogitization of the dominant Proterozoic orthogneisses during the short-lived UHP event. Subsequent exhumation to 8–10 km depth by about 375 Ma occurred at a much slower mean rate of about 1.3 mm a−1 with the late-stage extensional collapse of the Caledonian orogen playing an increasingly important role, especially in the final unroofing of the Western Gneiss Region with some remarkably preserved UHP rocks.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Journal of oral rehabilitation 32 (2005), S. 0 
    ISSN: 1365-2842
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: summary  The aim of this in vitro study was to determine the thermal mechanical properties of veneering composites after polymerization with the appropriate polymerization device. Fracture tests were performed to investigate the effect on fixed partial dentures (FPDs).Dynamic mechanical thermal analysis was used to determine the temperature-dependent mechanical properties. To approximate the clinical situation, the fracture resistance of three-unit metal-based FPDs with different composite veneering was investigated after a simulated 5-year oral wearing period. The restorations were made of a high gold alloy and veneered with three different composites. To determine the influence of fabrication, one composite was used in a light-polymerizing and a heat/pressure-curing version and, in addition, a newly developed heat protection paste was used. After a 5-year simulation period, the fracture resistance was determined.The storage modulus varied between 14268 N mm−2 (Belleglass) and 6616 N mm−2 (Sinfony). Adoro showed no significant differences between light curing (9155 N mm−2) and heat curing (8184 N mm−2) variations. The Adoro-veneering with the heat protection paste showed the highest median fracture strength (1700 N), followed by Adoro LC (1555 N), Belleglass (1051 N), Adoro HP (1150 N) and Sinfony (909 N). The most common failure type occurring in all FPDs was a cracking of the composite, exposing the metal framework. All FPDs showed stress cracking of the composite. The heat protection paste seemed to reduce the crack formation after fabrication and increased the fracture resistance of the composite veneering. Stress cracking after thermal cycling and mechanical loading affected all composites, but all veneered three-unit alloy FPDs showed a fracture resistance sufficient for posterior application.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 4339-4344 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Scanning optical microscopy with uncoated dielectric silica probe is used in the near field to investigate the propagation of optical modes along tapered integrated semiconductor optical amplifier devices and at larger working distances to study the electromagnetic intensity profile in the focal plane of various microlensed fibers. We show how this technique provides images of the mode structure of optoelectronic devices and profiled optical fibers with typical sizes in the range 2–10 μm, with an accuracy of 0.2 μm in beamwaist measurements. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Mass Spectrometry and Ion Processes 121 (1992), S. 201-240 
    ISSN: 0168-1176
    Keywords: negative thermal ion mass spectrometry ; secondary ion mass spectrometry ; sputter-induced resonance ionization mass spectrometry. ; thermal ion mass spectrometry
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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