CLONING AND EXPRESSION IN SACCHAROMYCES-CEREVISIAE OF THE NAD(P)H-DEPENDENT XYLOSE REDUCTASE-ENCODING GENE (XYL1) FROM THE XYLOSE-ASSIMILATING YEAST PICHIA-STIPITIS

被引:114
作者
AMORE, R [1 ]
KOTTER, P [1 ]
KUSTER, C [1 ]
CIRIACY, M [1 ]
HOLLENBERG, CP [1 ]
机构
[1] HEINRICH HEINE UNIV,INST MIKROBIOL,UNIV STR 1,W-4000 DUSSELDORF 1,GERMANY
关键词
GENE FUSION; TAC-XYL1-PROMOTER FUSION; HETEROLOGOUS GENE EXPRESSION; RECOMBINANT DNA; YEAST; ALDOSE REDUCTASE; PROTEIN SEQUENCE COMPARISON; XYLOSE FERMENTATION;
D O I
10.1016/0378-1119(91)90592-Y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The XYL1 gene of the yeast Pichia stipitis has been isolated from a genomic library using a specific cDNA probe, and its nucleotide (nt) sequence has been determined. In the 5' noncoding region of the P. stipitis XYL1 gene a TATAAA element (known to be necessary for transcription initiation in most yeast genes) is found at nt -81, and two CCAAT recognition motifs (often referred to as the CCAAT box) are present at nt -146 and -106. The XYL1 encodes a polypeptide of 35 927 Da that constitutes a NADH/NADPH-dependent xylose reductase (XR). The enzyme is part of the xylose-xylulose pathway that is absent or only weakly expressed in Saccharomyces cerevisiae. Extensive homology is found to the N terminus of the XR of Pachysolen tannophilus and Candida shehatae. None of the known cofactor binding domains found in many NAD-dependent dehydrogenases are present in the protein. Transformants of S. cerevisiae containing XYL1 of P. stipitis synthesize an active XR. Fusion of XYL1 with the prokaryotic tac promoter leads to a gene that can be expressed in S. cerevisiae and Escherichia coli.
引用
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页码:89 / 97
页数:9
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