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- W2018980750 abstract "Abstract A 3-kbp DNA fragment including the l -2,3-butanediol dehydrogenase ( l -BDH) gene ( bud C) from the chromosomal DNA of Brevibacterium saccharolyticum C-1012 was cloned in Escherichia coli JM109 after its insertion into pBluescript II SK + , and the resulting plasmid was named pLBD-SK. The bud C had an open reading frame consisting of 774 bp and encoded 258 amino acids. It was not included in a 2,3-butanediol operon such as is seen in the case of the meso -BDH gene ( bud C) of Klebsiella pneumoniae . For the expression of the bud C, the deletion plasmid pLBD2-119 was prepared from pLBD-SK. E. coli JM109/pLBD2-119 had higher l -BDH activity than that of Br. saccharolyticum C-1012. The l -BDH appeared as two bands on disc-PAGE. Isopropyl-β- d -thiogalacto-pyranoside (IPTG) influenced the quantity radio of the electrophoretic isoenzymes of l -BDH from E. coli JM109/pLBD2-119 that is, a higher relative mobility band with weak substrate specificity was abundantly produced by IPTG. The BDH was considered to belong to the short-chain dehydrogenase/reductase (SDR) family on the basis of the following distinctive features: it possessed two conservative sequences GXXXGXG and YXXXK, and it consisted of about 250 amino acids. As a result of a phylogenetic analysis of SDR family enzymes, the BDHs were considered to comprise a cluster independent from the other SDR enzymes." @default.
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- W2018980750 date "1998-01-01" @default.
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- W2018980750 title "Cloning, expression and nucleotide sequence of the l-2,3-butanediol dehydrogenase gene from Brevibacterium saccharolyticum C-1012" @default.
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