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Substituent Effects in the Carboxypeptidase A Catalyzed Hydrolysis of Substituted L,.beta.-Phenyllactate Esters

✍ Scribed by Osumi, Alan; Rahmo, Abdulkader; King, Stephen W.; Przystas, Theodore J.; Fife, Thomas H.

Book ID: 127306798
Publisher: American Chemical Society
Year: 1994
Tongue: English
Weight: 928 KB
Volume: 33
Category: Article
ISSN: 0006-2960
DOI: 10.1021/bi00253a013

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Results of a previous study on the hydrolysis of \(O\)-( \(\alpha\)-acylamino-cinnamoyl)-L- \(\beta\)-phenyllactates \(E 1\) and \(\mathbf{E} 2\) catalyzed by carboxypeptidase \(A(C P A)\) supported the anhydride mechanism for the action of CPA. Since these esters are hydrolyzed very slowly by CPA,