CLONING OF THE ALDEHYDE REDUCTASE GENE FROM A RED YEAST, SPOROBOLOMYCES SALMONICOLOR, AND CHARACTERIZATION OF THE GENE AND ITS PRODUCT

Citation
K. Kita et al., CLONING OF THE ALDEHYDE REDUCTASE GENE FROM A RED YEAST, SPOROBOLOMYCES SALMONICOLOR, AND CHARACTERIZATION OF THE GENE AND ITS PRODUCT, Applied and environmental microbiology, 62(7), 1996, pp. 2303-2310
Citations number
35
Categorie Soggetti
Microbiology,"Biothechnology & Applied Migrobiology
ISSN journal
00992240
Volume
62
Issue
7
Year of publication
1996
Pages
2303 - 2310
Database
ISI
SICI code
0099-2240(1996)62:7<2303:COTARG>2.0.ZU;2-3
Abstract
An NADPH-dependent aldehyde reductase (ALR) isolated from a red yeast, Sporobolomyces salmonicolor, catalyzes the reduction of a variety of carbonyl compounds. To investigate its primary structure, we cloned an d sequenced the cDNA coding for ALR. The aldehyde reductase gene (ALR) comprises 969 bp and encodes a polypeptide of 35,232 Da. The deduced amino acid sequence showed a high degree of similarity to other member s of the aldo-keto reductase superfamily. Analysis of the genomic DNA sequence indicated that the ALR gene was interrupted by six introns (t wo in the 5' noncoding region and four in the coding region). Southern hybridization analysis of the genomic DNA from S. salmonicolor indica ted that there was one copy of the gene. The ALR gene was expressed in Escherichia coli under the control of the tac promoter. The enzyme ex pressed in E. coli was purified to homogeneity and showed the same cat alytic properties as did the enzyme from S. salmonicolor.