Literature DB >> 8053906

Interactions of plant acetohydroxy acid isomeroreductase with reaction intermediate analogues: correlation of the slow, competitive, inhibition kinetics of enzyme activity and herbicidal effects.

R Dumas1, C Cornillon-Bertrand, P Guigue-Talet, P Genix, R Douce, D Job.   

Abstract

N-Hydroxy-N-isopropyloxamate (IpOHA) is known to inhibit extremely tightly (Ki of 22 pM) the bacterial acetohydroxy acid isomeroreductase (EC 1.1.1.86) [Aulabaugh and Schloss (1990) Biochemistry 29, 2824-2830], the second enzyme of the branched-chain-amino-acid-biosynthetic pathway. Yet, although the same pathway exists in plant cells, this compound presents only very poor herbicidal action. Towards the goal of gaining a better understanding of this behaviour, we have studied the mechanism of interaction of this compound with a highly purified acetohydroxy acid isomeroreductase of plant origin, i.e. the spinach (Spinacia oleracea) chloroplast enzyme. IpOHA behaved as a nearly irreversible inhibitor of the enzyme. Encounter complex formation was very slow (association rate constant 1.9 x 10(3) M-1.s-1) and involved a single bimolecular step. Since inhibition was competitive with respect to acetohydroxy acid substrates, the time needed to achieve substantial (90%) inhibition in vitro of enzyme activity in the simultaneous presence of substrates and inhibitors was extremely long (for example of the order of hours at 1 microM IpOHA and 100 microM acetohydroxy acid substrates). Thus, under in vivo conditions, binding of the inhibitor may be so slow that it may delay considerably the time required for inhibition of the target enzyme. Simialr kinetic behaviour was observed with another reaction intermediate analogue described by Schulz, Spönemann, Köcher and Wengenmayer [(1988) FEBS Lett. 238, 375-378], 2-dimethyl-phosphinoyl-2-hydroxyacetic acid (Hoe 704), which displays a higher herbicide activity than IpOHA. The herbicidal potency of these two compounds appeared to be correlated with their rates of association with the plant acetohydroxy acid isomeroreductase, since the bimolecular rate constant for Hoe 704 (2.2 x 10(4) M-1.s-1) was higher than that for IpOHA.

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Year:  1994        PMID: 8053906      PMCID: PMC1137060          DOI: 10.1042/bj3010813

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  26 in total

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Authors:  J Ricard; J Buc; J C Meunier
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2.  Purification and properties of the acetohydroxy acid isomeroreductase of Salmonella typhimurium.

Authors:  S M Arfin; H E Umbarger
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3.  Kinetic aspects of regulation of metabolic processes. The hysteretic enzyme concept.

Authors:  C Frieden
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Authors:  K E Neet; G R Ainslie
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

5.  Kinetics of the reversible inhibition of enzyme-catalysed reactions by tight-binding inhibitors.

Authors:  J F Morrison
Journal:  Biochim Biophys Acta       Date:  1969

6.  Isolation, characterization and sequence analysis of a full-length cDNA clone encoding acetohydroxy acid reductoisomerase from spinach chloroplasts.

Authors:  R Dumas; M Lebrun; R Douce
Journal:  Biochem J       Date:  1991-07-15       Impact factor: 3.857

7.  Purification and characterization of acetohydroxyacid reductoisomerase from spinach chloroplasts.

Authors:  R Dumas; J Joyard; R Douce
Journal:  Biochem J       Date:  1989-09-15       Impact factor: 3.857

8.  Isolation and kinetic properties of acetohydroxy acid isomeroreductase from spinach (Spinacia oleracea) chloroplasts overexpressed in Escherichia coli.

Authors:  R Dumas; D Job; J Y Ortholand; G Emeric; A Greiner; R Douce
Journal:  Biochem J       Date:  1992-12-15       Impact factor: 3.857

9.  Nucleotide sequence and characterization of a cDNA encoding the acetohydroxy acid isomeroreductase from Arabidopsis thaliana.

Authors:  G Curien; R Dumas; R Douce
Journal:  Plant Mol Biol       Date:  1993-02       Impact factor: 4.076

10.  Branched-chain-amino-acid biosynthesis in plants: molecular cloning and characterization of the gene encoding acetohydroxy acid isomeroreductase (ketol-acid reductoisomerase) from Arabidopsis thaliana (thale cress).

Authors:  R Dumas; G Curien; R T DeRose; R Douce
Journal:  Biochem J       Date:  1993-09-15       Impact factor: 3.857

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2.  The crystal structure of plant acetohydroxy acid isomeroreductase complexed with NADPH, two magnesium ions and a herbicidal transition state analog determined at 1.65 A resolution.

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4.  Metabolic effects of inhibitors of two enzymes of the branched-chain amino acid pathway in Salmonella typhimurium.

Authors:  S Epelbaum; D M Chipman; Z Barak
Journal:  J Bacteriol       Date:  1996-02       Impact factor: 3.490

5.  Molecular annotation of ketol-acid reductoisomerases from Streptomyces reveals a novel amino acid biosynthesis interlock mediated by enzyme promiscuity.

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Journal:  Microb Biotechnol       Date:  2014-10-09       Impact factor: 5.813

6.  NADH/NADPH bi-cofactor-utilizing and thermoactive ketol-acid reductoisomerase from Sulfolobus acidocaldarius.

Authors:  Chin-Yu Chen; Tzu-Ping Ko; Kuan-Fu Lin; Bo-Lin Lin; Chun-Hsiang Huang; Cheng-Hung Chiang; Jia-Cherng Horng
Journal:  Sci Rep       Date:  2018-05-08       Impact factor: 4.379

7.  Dihydroxy-Acid Dehydratases From Pathogenic Bacteria: Emerging Drug Targets to Combat Antibiotic Resistance.

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Journal:  Chemistry       Date:  2022-06-16       Impact factor: 5.020

  7 in total

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