ACYLATION OF THE ENZYMATIC SITE OF δ-CHYMOTRYPSIN BY ESTERS, ACID ANHYDRIDES, AND ACID CHLORIDES
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چکیده
منابع مشابه
Mechanisms of acylation of chymotrypsin by phenyl esters of benzoic acid and acetic acid.
The kinetics of the acylation of alpha-chymotrypsin by a series of substituted phenyl p-nitrobenzoates have been studied by stopped flow and conventional spectrophotometry. Electron withdrawal in the leaving group accelerates the rate of acylation, and the p value obtained for eight esters is +1.96. The pH- and pD-independent acylation rate constants are, respectively, 1.40 X 10(4) M-1S-1 and 1...
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چکیده ندارد.
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Trialkylamine-mediated intramolecular cyclization of pent-4-enoyl chlorides was studied. Substitution with a tertiary alkyl group at the 2-position gave cyclopent-2-en-1-ones, while substitution with an aromatic group gave enol esters, which were formed by O-acylation of initially formed 3-chlorocyclopentanones with ketenes.
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Enzymatic synthesis of sugar fatty acid esters was performed in an organic solvent using an immobilized Candida antartica lipase and various sugars and oleic acid as substrates. A high solubility of the sugar in the solvent was needed for a high sugar ester yield. Among the sugars and solvents tested in this study, the highest yield (98 %) was obtained when xylitol and 2-methyl 2-butanol were u...
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ژورنال
عنوان ژورنال: Journal of Biological Chemistry
سال: 1957
ISSN: 0021-9258
DOI: 10.1016/s0021-9258(18)64900-2