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PMID: 1069272 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mechanism of action of carboxypeptidase A in ester hydrolysis.

Makinen MW, Yammura K, Kaiser ET

Abstract

The reaction of carboxypeptidase A (peptidyl-L-amino-acid hydrolase; EC 3.4.12.2) with the specific ester substrate O-(trans-p-chlorocinnamoyl)-L-beta-phenyllactate has been investigated in the temperature range 25 degrees to -40 degrees with use of organic-aqueous cosolvent mixtures. In the subzero temperature range the hydrolysis reaction is characterized by a biphasic decrease in absorbance specific for the substrate. The kinetic data can be unambigously analyzed as two consecutive first-order reactions with formation of a covalent acyl-enzyme intermediate. Deacylation of the covalent intermediate is shown to be rate-limiting in the subzero temperature range, and near -60 degrees it is sufficiently stable for spectral characterization. Consideration of the structure of the active site and of the catalytically functional residues of the enzyme leads to the conclusion that the intermediate is a mixed anhydride in which the gamma-carboxylate of glutamate-270 is acylated by the substrate. The temperature dependence of the rate constants of the acylation and deacylation steps explains why the intermediate of this enzyme-catalyzed reaction is observed only at low temperatures.

MeSH Terms
Binding Sites Carboxypeptidases/metabolism Catalysis Cold Temperature Kinetics
Chemicals
Carboxypeptidases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Makinen M W
Yammura K
Kaiser E T
References (11)
11 references, click to expand
  1. Spectrophotometric identification of acyl enzyme intermediates.
    Biochemistry. 1965 Jun;4(6):1108-18 PMID: 5839997
  2. Enzymology at sub-zero temperatures.
    Mol Cell Biochem. 1973 May 11;1(1):15-27 PMID: 4154398
  3. A potent reversible inhibitor of carboxypeptidase A.
    J Biol Chem. 1972 Jan 25;247(2):606-8 PMID: 5061899
  4. Ionic strength and protonic activity of supercooled solutions used in experiments with enzyme systems.
    J Biol Chem. 1973 Jul 10;248(13):4649-54 PMID: 4718738
  5. pH dependence of the nitrotyrosine-248 and arsanilazotyrosine-248 carboxypeptidase A catalyzed hydrolysis of O-(trans-p-chlorocinnamoyl)-L-beta-phenyllactate.
    J Am Chem Soc. 1976 Mar 31;98(7):1940-7 PMID: 3540
  6. Environment and conformation dependent sensitivity of the arsanilazotyrosine-248 carboxypeptidase A chromophore.
    Biochemistry. 1975 Feb 25;14(4):649-60 PMID: 234737
  7. Carboxypeptidase A: a protein and an enzyme.
    Adv Protein Chem. 1971;25:1-78 PMID: 4946703
  8. Circular dichroism-inhibitor titrations of arsanilazotyrosine-248 carboxypeptidase A.
    Biochemistry. 1976 Jan 27;15(2):296-303 PMID: 1247518
  9. A search for an intermediate in carboxypeptidase A catalyzed ester hydrolyses.
    J Am Chem Soc. 1970 Oct 7;92(20):6046-9 PMID: 5459197
  10. pPH dependence and competitive product inhibition of the carboxypeptidase A catalyzed hydrolysis of O-(trans-cinnamoyl)-L-beta-phenyllactate.
    J Am Chem Soc. 1969 Jan 15;91(2):485-91 PMID: 5782503
  11. pH dependence of the hydrolysis of O-acetyl-L-mandelate catalyzed by carboxypeptidase A. A critical examination.
    J Am Chem Soc. 1966 Mar 20;88(6):1212-23 PMID: 5905604
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1976-11-00
Pages
3882-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC431251
Subset
IM
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