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Identification and Characterization of a Mycobacterial (2R,3R)-2,3-Butanediol Dehydrogenase
Author(s) -
Minoru Takeda,
Takahiro Muranushi,
Sawako Inagaki,
Takuya Nakao,
Shigekazu Motomatsu,
Ichirō Suzuki,
Junichi Koizumi
Publication year - 2011
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1271/bbb.110607
Subject(s) - dehydrogenase , 2,3 butanediol , orfs , enzyme , biochemistry , alcohol dehydrogenase , homology (biology) , strain (injury) , biology , stereochemistry , gene , chemistry , open reading frame , peptide sequence , fermentation , anatomy
Bacterial strain B-009, capable of using racemic 1,2-propanediol (PD), was identified as a rapid-growing member of the genus Mycobacterium. The strain is phylogenetically related to M. gilvum, but has slightly different physiological characteristics. An NAD(+)-dependent enantioselective alcohol dehydrogenase, which acts on R-PD, was purified from the strain. The enzyme was a homodimer of a peptide coded by a 1047-bp gene (mbd1). A highly conserved sequence for medium-chain dehydrogenase/reductases with a preference for secondary alcohols was found in the gene. Hydroxyacetone was produced from R-PD by an enzymatic reaction, indicating that position 2 of the substrate was oxidized. The enzyme activity was highest for (2R,3R)-2,3-butanediol (R,R-BD), enabling the enzyme to be identified as (2R,3R)-2,3-butanediol dehydrogenase (R,R-BD-DH). A homology search revealed M. gilvum, M. vanbaalenii, and M. semegmatis to have ORFs similar to mbd1, suggesting the widespread distribution of genes encoding R,R-BD-DH among mycobacterial strains.

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