Conversion of the coenzyme specificity of isocitrate dehydrogenase by module replacement

The coenzyme specificity of isocitrate dehydrogenase from an extreme thermophilic bacterium was converted from NADP-dependent to NAD-dependent by replacing a "module" involved in the coenzyme binding site. The conversion was not possible with the replacement of a few residues that interact...

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Veröffentlicht in:Journal of biochemistry (Tokyo) 1996-05, Vol.119 (5), p.1014-1018
Hauptverfasser: Yaoi, T, Miyazaki, K, Oshima, T, Komukai, Y, Go, M
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Sprache:eng
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Zusammenfassung:The coenzyme specificity of isocitrate dehydrogenase from an extreme thermophilic bacterium was converted from NADP-dependent to NAD-dependent by replacing a "module" involved in the coenzyme binding site. The conversion was not possible with the replacement of a few residues that interact with the coenzyme. In addition, the module-replaced mutant dehydrogenase was as stable as the original, wild type enzyme. The results support a previous hypothesis that a module is a structural and functional unit of a protein.
ISSN:0021-924X
1756-2651
DOI:10.1093/oxfordjournals.jbchem.a021316