Cloning, expression and regulation of Schizosaccharomyces pombe gene encoding thioltransferase

被引:10
作者
Cho, YW
Kim, HG
Park, EH
Fuchs, JA
Lim, CJ [1 ]
机构
[1] Kangweon Natl Univ, Coll Nat Sci, Div Life Sci, Chunchon 200701, South Korea
[2] Sookmyung Womens Univ, Coll Pharm, Seoul 140742, South Korea
[3] Univ Minnesota, Dept Biochem Mol Biol & Biophys, St Paul, MN 55108 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2000年 / 1517卷 / 01期
关键词
cloning; fission yeast; thioltransferase; Schizosaccharomyces pombe;
D O I
10.1016/S0167-4781(00)00242-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genomic DNA encoding thioltransferase was isolated from Schizosaccharomyces pombe using the polymerase chain reaction. The amplified DNA fragment was confirmed by Southern hybridization, completely digested with HindIII and BamHI, and then ligated into the yeast-Escherichia coli shuttle vector pRS316, which resulted in plasmid pEH1. The insert of plasmid pEH1 was transferred into the multicopy vector YEp357 to generate plasmid pYEH1. The determined nucleotide sequence harbors an open reading frame consisting of four exons and three introns, which encodes a polypeptide of 101 amino acids with a molecular mass of 11 261 Da. Thioltransferase activity was increased 1.6-fold in Saccharomyces cerevisiae containing plasmid pYEH1, and 1.8- and 2.7-fold in S. pombe containing plasmid pEH1 and pYEH1, respectively. The upstream sequence and the region encoding the N-terminal six amino acids were fused into promoterless beta -galactosidase gene of the shuttle vector YEp357R to generate the fusion plasmid pYEHR1. Synthesis of beta -galactosidase from the fusion plasmid was found to be enhanced by zinc and NO-generating S-nitroso-N-acetylpenicillamine. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:171 / 175
页数:5
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