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Ammonium bacterial

Inhibitors as well as substrates bind in this crevice between the domains. From the numerous studies of different inhibitors bound to serine pro-teinases we have chosen as an illustration the binding of a small peptide inhibitor, Ac-Pro-Ala-Pro-Tyr-COOH to a bacterial chymotrypsin (Figure 11.9). The enzyme-peptide complex was formed by adding a large excess of the substrate Ac-Pro-Ala-Pro-Tyr-CO-NHz to crystals of the enzyme. The enzyme molecules within the crystals catalyze cleavage of the terminal amide group to produce the products Ac-Pro-Ala-Pro-Tyr-COOH and NHs. The ammonium ions diffuse away, but the peptide product remains bound as an inhibitor to the active site of the enzyme. [Pg.211]

There is evidence the drug acts as an antimetabolite for the i ira-aminobenzoic acid required for bacterial metabolism.) One oT the more recent of the many preparations for this drug involves carboxylation of meta-aminophenol (6) by means of ammonium i.ii bonate under high pressure. ... [Pg.109]

Ohara M, Y Katayama, M Tsuzaki, S Nakamoto, H Kuraishi (1990) Paracoccus kocurii sp. nov., a tetramethyl-ammonium-assrmilating bacterium. Int J Syst Bacterial 40 292-296. [Pg.332]

Forward approach, to qualitative reliability analysis, 26 984 Forward-roll coaters, 7 12-13 method summarized, 7 5t shear rates, 7 32t Fosamine-ammonium, 13 320 Fosfomycin, bacterial resistance mechanisms, 3 32t... [Pg.378]

The dried bacteria also contain invertase and this hydrolytic enzyme competes with the sucrose phosphorylase for sucrose. However, it is possible to eliminate most of the invertase from the bacterial preparations by several precipitations with ammonium sulfate. Using a partially purified sucrose phosphorylase preparation and a mixture of... [Pg.46]

The last paper in this category describes monitoring of a submerged filamentous bacterial cultivation.38 Arnold et al. studied a 12-1 stirred tank where a strain of Streptomyces fradiae was used for fermentation. They followed ammonium, methyl oleate, glucose, and glutamate concentrations over time in the production of tylosin. [Pg.392]

A potentiometric determination of lysozyme is based on a system similar to a bacterial electrode [11]. The cells of the bacteria, Mcrococcus lysodeicticus, readily accept trimethylphenyl ammonium ions (TMPA ) from the solution. Lysozyme decomposes the cell membranes and TMPA is liberated. The rate... [Pg.204]

Biooxidation by cometabolization with methane or ammonium Removal by ferrous or manganese ions produced by bacterial reduction of Fe(III) and Mn(IV)... [Pg.138]

The amoimt of ammonium sulfate resulting from the previous precipitation has to he taken into consideration Data from Jones GL, Hebert GA, Cherry WB (1978) Flnorescent antibody techniqnes and bacterial applications. H.E.W. Pnbl., Atlanta... [Pg.146]

Initially, the antibodies should be purified prior to prepare the immunoaffinity column. Precipitation with ammonium sulfate, ion-exchange chromatography, gel filtration chraoma-tography or affinity chromatography may be employed with the aim of antibody purification. Activated beads which are coated with bacterial proteins A or G may be used as the support material. Some parameters may be changed for the elution of the sample solution for example the ionic conditions of mobile phase may be changed or chaotropic buffers may be used [11]. [Pg.89]


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