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. 1981 Mar 1;193(3):819–823. doi: 10.1042/bj1930819

Evidence that the lack of high catalytic activity of thiolsubtilisin towards specific substrates may be due to an inappropriately located proton-distribution system. Demonstration of highly nucleophilic character of the thiol group of thiolsubtilisin in the catalytically relevant ionization state of the active centre by use of a two-protonic-state reactivity probe.

K Brocklehurst, J P Malthouse
PMCID: PMC1162672  PMID: 6272719

Abstract

The active centre of the semi-synthetic enzyme thiolsubtilisin was investigated by studying the kinetics of the reaction of the thiol group of cysteine-221 with the thiol-specific two-protonic-state reactivity probe 2,2'-dipyridyl disulphide. The three-states criterion [Brocklehurst (1974) Tetrahedron 30, 2397-2407] was used to provide definitive evidence of the existence of a thiol--imidazole interactive system in acidic media in which the sulphur atom possesses highly nucleophilic character. The lack of catalytic competence of thiolsubtilisin despite its possession of the requisite nucleophilic capability is discussed. The exceedingly high rate of reaction of thiolsubtilisin with 2,2'-dipyridyl disulphide at pH 4--5 is shown to constitute a rapid and convenient active-site titration in which intact thiol--imidazole interaction is detected even in the presence of other thiols.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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