Literature DB >> 3626585

Progress curves of reactions catalyzed by unstable enzymes. A theoretical approach.

R G Duggleby.   

Abstract

When an enzyme is incubated with its substrate, the rate of catalysis will decline with time due to the combined effects of substrate utilization and product accumulation. These effects will be superimposed upon a progressive loss of catalytic activity if the enzyme is unstable, either spontaneously or as a result of an added reagent. In this report, the effect of enzyme inactivation on the progress curve for an enzyme-catalyzed reaction is considered. It is shown that under most circumstances catalysis will stop before the substrate is totally exhausted and that the amount of substrate remaining is related to the inactivation rate constants for various intermediates on the catalytic pathway. A graphical method for estimating these inactivation rate constants is suggested for several situations, including one which encompasses the effect of a suicide substrate. Expressions for the half time of the reaction are also given for some special cases.

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Year:  1986        PMID: 3626585     DOI: 10.1016/s0022-5193(86)80236-3

Source DB:  PubMed          Journal:  J Theor Biol        ISSN: 0022-5193            Impact factor:   2.691


  8 in total

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Authors:  Peter V Vrzheshch; Elena A Batanova; Alevtina T Mevkh; Sergei D Varfolomeev; Irina G Gazaryan; Roger N F Thorneley
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2.  Kinetics of inactivation of bovine pancreatic ribonuclease A by bromopyruvic acid.

Authors:  M H Wang; Z X Wang; K Y Zhao
Journal:  Biochem J       Date:  1996-11-15       Impact factor: 3.857

3.  Mechanism and kinetics of inducible nitric oxide synthase auto-S-nitrosation and inactivation.

Authors:  Brian C Smith; Nathaniel B Fernhoff; Michael A Marletta
Journal:  Biochemistry       Date:  2012-01-24       Impact factor: 3.162

4.  Resistance to inactivation by EGTA of the enzyme-substrate and enzyme-phosphate complexes of alkaline phosphatase.

Authors:  S J Pike; R G Duggleby
Journal:  Biochem J       Date:  1987-06-15       Impact factor: 3.857

5.  Kinetic analysis of a Michaelis-Menten mechanism in which the enzyme is unstable.

Authors:  C Garrido-del Solo; F García-Cánovas; B H Havsteen; R Varón-Castellanos
Journal:  Biochem J       Date:  1993-09-01       Impact factor: 3.857

6.  Kinetics of an enzyme reaction in which both the enzyme-substrate complex and the product are unstable or only the product is unstable.

Authors:  C Garrido-del Solo; F García-Cánovas; B H Havsteen; E Valero; R Varón
Journal:  Biochem J       Date:  1994-10-15       Impact factor: 3.857

7.  Mutations of penicillin acylase residue B71 extend substrate specificity by decreasing steric constraints for substrate binding.

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Journal:  Biochem J       Date:  2003-04-01       Impact factor: 3.857

Review 8.  Time-dependent enzyme inactivation: Numerical analyses of in vitro data and prediction of drug-drug interactions.

Authors:  Jaydeep Yadav; Erickson Paragas; Ken Korzekwa; Swati Nagar
Journal:  Pharmacol Ther       Date:  2019-12-11       Impact factor: 12.310

  8 in total

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