Titlebook: Enzyme Engineering; Volume 5 Howard H. Weetall,Garfield P. Royer Book 1980 Springer Science+Business Media New York 1980 Fermentation.Gluco

FLIT

狂热文化

Comparative Quantitative Physiology of High Cellulase Producing Strains of ,a, QM 9414, C 30 (7) and MCG 77 (3). These strains were then compared in terms of specific enzyme productivity, the nutrient requirements and economics, the nature of cellulase components, and the stability and utilization efficiency of cellulase.

Foment

Bacterial Exo-Enzyme and Exo-Toxin Exporte releasing protease respectively, with this penicillinase and other exo-proteins suggest a common export mechanism for proteins. However, recent findings on the nature of the exo-penicillinase precursor cast doubt on this mechanism and its ubiquity.

Pde5-Inhibitors

Enzyme Purification by Liquid-Liquid Extraction were used for constituting the two-phase systems. Using the latter which show a rather high rate of phase separation we are trying to enhance the effectivity of the phase partition method by developing continuous countercurrent procedures.

accrete

Continuous Isolation of Yeast-Lytic Enzymes from Citophaga hand, enzymic lysis can also complement mechanical cell disruption by producing the degradation and solubilization of the cell wall. For this, a suitable enzyme has to be efficiently produced and isolated.

自由职业者

Immobilized Tannin as Protein Adsorbent-Preparation, Characteristics, and Applicationsnorganic compounds together with proteins. We feel that if an adsorbent that specifically adsorbed proteins could be prepared, it would be of great advantage in many scientific fields. To design this adsorbent, we chose tannin as our ligand.

VEN

Aminoalkylpolysaccharide Sorbents in Purification of Enzymesons play an important role. These electrostatic forses may be of the same or the oppsite sign. As a result of these interaction, the factors such as of sorbion-elution medium, all effect the sorbtion of the protein.

Frequency

冥界三河

裂口

Jörg Neugebauer,Chris G. Van de Walleell (1–6). Our interest has been in the direct type enzyme fuel cell, with the glucose oxidase-flavin cofactor system as a model anoidc catalyst. The objective of this paper is to discuss the chemical modification of the electrode surface, as an approach to improved enzyme catalyzed fuel cells, with special emphasis on flavin cofactor systems.