RRC ID |
27480
|
著者 |
Isotani K, Kurokawa J, Suzuki F, Nomoto S, Negishi T, Matsuda M, Itoh N.
|
タイトル |
Gene cloning and characterization of two NADH-dependent 3-quinuclidinone reductases from Microbacterium luteolum JCM 9174.
|
ジャーナル |
Appl Environ Microbiol
|
Abstract |
We used the resting-cell reaction to screen approximately 200 microorganisms for biocatalysts which reduce 3-quinuclidinone to optically pure (R)-(-)-3-quinuclidinol. Microbacterium luteolum JCM 9174 was selected as the most suitable organism. The genes encoding the protein products that reduced 3-quinuclidinone were isolated from M. luteolum JCM 9174. The bacC gene, which consists of 768 nucleotides corresponding to 255 amino acid residues and is a constituent of the bacilysin synthetic gene cluster, was amplified by PCR based on homology to known genes. The qnr gene consisted of 759 nucleotides corresponding to 252 amino acid residues. Both enzymes belong to the short-chain alcohol dehydrogenase/reductase (SDR) family. The genes were expressed in Escherichia coli as proteins which were His tagged at the N terminus, and the recombinant enzymes were purified and characterized. Both enzymes showed narrow substrate specificity and high stereoselectivity for the reduction of 3-quinuclidinone to (R)-(-)-3-quinuclidinol.
|
巻・号 |
79(4)
|
ページ |
1378-84
|
公開日 |
2013-2-1
|
DOI |
10.1128/AEM.03099-12
|
PII |
AEM.03099-12
|
PMID |
23263947
|
PMC |
PMC3568593
|
MeSH |
Actinomycetales / enzymology*
Actinomycetales / genetics
Amino Acid Sequence
Cloning, Molecular
Coenzymes / metabolism*
DNA, Bacterial / chemistry
DNA, Bacterial / genetics
Escherichia coli / genetics
Molecular Sequence Data
NAD / metabolism*
Oxidoreductases / genetics*
Oxidoreductases / metabolism*
Quinuclidines / metabolism*
Recombinant Fusion Proteins / genetics
Recombinant Fusion Proteins / isolation & purification
Sequence Alignment
Sequence Analysis, DNA
Substrate Specificity
|
IF |
4.016
|
引用数 |
10
|
WOS 分野
|
BIOTECHNOLOGY & APPLIED MICROBIOLOGY
MICROBIOLOGY
|
リソース情報 |
一般微生物 |
JCM 3705
JCM 9171
JCM 9174 |