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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Analytical Biochemistry 91 (1978), S. 158-165 
    ISSN: 0003-2697
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Enzyme and Microbial Technology 16 (1994), S. 795-801 
    ISSN: 0141-0229
    Keywords: Lysozyme ; electrosynthesis ; tyrosine
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Thin Solid Films 244 (1994), S. 1012-1017 
    ISSN: 0040-6090
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Biotechnology letters 7 (1985), S. 581-584 
    ISSN: 1573-6776
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Cultures ofAspergillus fumigatus IMI 246651, ATCC 46324 produced extracellular xylanase when grown on xylans, grasses and cereal straws. The activity was separable into three main groups of proteins by gel-filtration chromatography, the type and amount of each one depending upon the growth substrate.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Biotechnology letters 4 (1982), S. 459-464 
    ISSN: 1573-6776
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Phosphoric acid swollen cellulose has been reduced with3H-KBH4 and the resulting radioactive amorphous cellulose is broken down by a number of cellulolytic bacteria and fungi with accumulation of radioactive label in the culture filtrate. This is detected by scintillation counting. Non-cellulolytic microorganisms do not behave in a similar manner.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 8 (1998), S. 47-52 
    ISSN: 1057-9257
    Keywords: ligand gated ; channel protein ; biomembrane ; biosensor ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: We demonstrate a novel protective configuration for a gated channel biosensor. The bilayer membrane containing the channel proteins is formed by a simple self-assembly technique ensuring continuous coverage of the interface between two slabs of agarose gel by a biomimetic lamella in a fluid state. The gel protects both membrane surfaces from mechanical shock and contact with low-energy media while allowing diffusion of biomolecules up to 10 MDa in weight. The technique has been demonstrated using both dioleoyl-phosphatidylcholine (DOPC) and a phosphatidylcholine lipid cross-linked with a short polysiloxane chain (PSPC). The conductance per unit area of the channel-free membrane produced by this method was less than 25 S m-2 for DOPC and 2 S m-2 for PSPC, and the bilayer nature of the barrier in both cases has been demonstrated by measurement of the capacitance. The applicability to sensors has been confirmed using gramicidin-D, a 1·1 kDa unilamellar lipid bilayer pore former, and partially confirmed using valinomycin, a selective ion transporter. On incorporation of gramicidin the membrane conductance increased by over an order of magnitude. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 8 (1998), S. 101-105 
    ISSN: 1057-9257
    Keywords: biosensor ; protein immobilisation ; protein modification ; electrochemistry ; nitrotyrosine ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: Use of electrosynthetic methodology allows the production of hen egg-white lysozyme (HEWL) either mononitrated at tyrosine 23 or bisnitrated at tyrosines 20 and 23, but never nitrated at tyrosine 53. This is a different sequence from that obtained by the chemical nitrating agent tetranitromethane, and when reduced by dithionite, the selectively modified enzyme can be anchored at pH 5 via the unique aromatic amino group to magnetic beads or other suitable matrices. HEWL so immobilised loses less than 10% of cell-wall lytic activity compared with the approximately 50% loss of activity when immobilised by conventional methodology at pH 9 via essentially random reaction at lysine residues and other functionalities which are nucleophilic at this pH. This result offers promise as a general method for selective protein immobilisation in biosensors and similar applications. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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