Separation of the two reactions, oxidation and isomerization, catalyzed by Streptomyces cholesterol oxidase

Mitsuo Yamashita, Mitsutoshi Toyama, Hisayo Ono, Isao Fujii, Noriaki Hirayama, Yoshikatsu Murooka

Research output: Contribution to journalArticle

37 Citations (Scopus)

Abstract

Site-directed mutagenesis was used to identify key amino acid residues of the cholesterol oxidase from Streptomyces sp., which catalyzes the oxidation of cholesterol and the isomerization of 5-cholesten-3-one. Eight mutant enzymes were constructed and the following amino acid substitutions were identified: N318A, N318H, E356A, E356D, H441A, H441N, N480A and N480Q. Mutants N318A and N318H retained both oxidation and isomerization activities. The mutant E356D retained oxidation but not isomerization activity. On the other hand, mutants N480A and N480Q showed no oxidation activity but retained their isomerization activities. The two catalytic reactions, oxidation and isomerization, in cholesterol oxidase were thus successfully separated. When the H441A or H441N mutation was introduced, both the oxidase and isomerase activities were completely lost. The H441, E356 and N480 residues thus appear to participate in the catalysis of cholesterol oxidase, whereas N318 does not. An analysis of the products of these mutant enzymes suggested that the previously proposed 6-hydroxylation reaction by cholesterol oxidase is actually autooxidation from 5-cholesten-3-one. Kinetic studies of the purified wild-type and mutant enzymes showed that the k(cat)/K(m) values for oxidation in E356D and for isomerization in N480A increased six- and threefold, respectively, over those in the wild-type. These mutational effects and the reaction mechanisms are discussed in terms of the three-dimensional structure of the enzyme constructed on the basis of homology modeling.

Original languageEnglish
Pages (from-to)1075-1081
Number of pages7
JournalProtein Engineering
Volume11
Issue number11
Publication statusPublished - 1998 Nov
Externally publishedYes

Fingerprint

Cholesterol Oxidase
Cholesterol
Isomerization
Oxidation
Thermodynamic properties
Enzymes
Amino acids
Amino Acids
Isomerases
Hydroxylation
Mutagenesis
Catalysis
Oxidoreductases
Substitution reactions
Kinetics

Keywords

  • Cholesterol oxidase
  • Reaction mechanism
  • Separation of reactions
  • Streptomyces
  • Structural characterization

ASJC Scopus subject areas

  • Molecular Biology
  • Biochemistry

Cite this

Yamashita, M., Toyama, M., Ono, H., Fujii, I., Hirayama, N., & Murooka, Y. (1998). Separation of the two reactions, oxidation and isomerization, catalyzed by Streptomyces cholesterol oxidase. Protein Engineering, 11(11), 1075-1081.

Separation of the two reactions, oxidation and isomerization, catalyzed by Streptomyces cholesterol oxidase. / Yamashita, Mitsuo; Toyama, Mitsutoshi; Ono, Hisayo; Fujii, Isao; Hirayama, Noriaki; Murooka, Yoshikatsu.

In: Protein Engineering, Vol. 11, No. 11, 11.1998, p. 1075-1081.

Research output: Contribution to journalArticle

Yamashita, M, Toyama, M, Ono, H, Fujii, I, Hirayama, N & Murooka, Y 1998, 'Separation of the two reactions, oxidation and isomerization, catalyzed by Streptomyces cholesterol oxidase', Protein Engineering, vol. 11, no. 11, pp. 1075-1081.
Yamashita, Mitsuo ; Toyama, Mitsutoshi ; Ono, Hisayo ; Fujii, Isao ; Hirayama, Noriaki ; Murooka, Yoshikatsu. / Separation of the two reactions, oxidation and isomerization, catalyzed by Streptomyces cholesterol oxidase. In: Protein Engineering. 1998 ; Vol. 11, No. 11. pp. 1075-1081.
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