Gebundene Ausgabe. VI, 238 Seiten; Innen wie außen ein sehr gutes Exemplar. Die Leseseiten sind tadellos, sauber und ohne Anstreichungen. Sehr guter Zustand. 9783540649670 Sprache: Englisch Gewicht in Gramm: 1000.
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In den WarenkorbZustand: Used. pp. 252 52:B&W 6.14 x 9.21in or 234 x 156mm (Royal 8vo) Case Laminate on White w/Gloss Lam.
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Sprache: Englisch
Verlag: Springer Berlin Heidelberg, 1998
ISBN 10: 3540649670 ISBN 13: 9783540649670
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In den WarenkorbGebunden. Zustand: New. This review series covers actual trends in modern biologyAll aspects of this interdisciplinary technology, where knowledge, methods and expertise are required from chemistry, biochemistry, microbiology, genetics, chemical engineering and computerscience.
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In den WarenkorbHardcover. Zustand: Brand New. 9.75x6.50x0.75 inches. In Stock.
Sprache: Englisch
Verlag: Springer, Berlin, Springer, 1998
ISBN 10: 3540649670 ISBN 13: 9783540649670
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Buch. Zustand: Neu. Neuware - The immobilized biocatalyst (IMB) is a key component of biotransformation systems that are used to transform substrates to desired products. The impro- ment of biocatalyst properties has a direct influence on the overall effectiveness of the process based on the biotransformation. The basic catalytic characte- stics of biocatalyst that are followed include kinetic properties, pH optima, stability,and inhibition. The investigation of catalytic properties of immobilized enzymes is still a time consuming procedure and is not always simple. In the 1980s,a major effort was made to standardize the rules by which IMB is char- terized. The Working Party of EFB on immobilized biocatalysts has formul- ed principles of individual methods, among them the requirement of kinetic characterization [1]. It was recommended to use a packed-bed reactor,equipped with temperature control and with infinite flow circulation. The system should be equipped with a post-column unit to measure the time-dependence of the product or substrate concentration [2, 3], the most commonly used analytical methods being spectrophotometry, chemiluminiscence, automatic titration, bioluminiscence, chromatography, polarimetry, and biosensors based on the oxygen electrode. There are two main drawbacks to the application of these methods: 1. The need to vary the analytical principles, depending on the chemical and physical-chemical properties of analytes; 2. In some cases, mainly in the study of hydrolytic enzymes, the natural s- strate must be replaced by an artificial one,that is chromolytic,chromogenic, chemiluminiscent,bioluminiscent,or fluorescent.