首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Cloning, expression and regulation of Schizosaccharomyces pombe gene encoding thioltransferase
【24h】

Cloning, expression and regulation of Schizosaccharomyces pombe gene encoding thioltransferase

机译:巯基转移酶编码粟酒裂殖酵母基因的克隆,表达及调控

获取原文
获取原文并翻译 | 示例
       

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 β-galactosidase gene of the shuttle vector YEp357R to generate the fusion plasmid pYEHRl. Synthesis of β-galactosidase from the fusion plasmid was found to be enhanced by zinc and NO-generating S-nitroso-N-acetylpenicillamine.
机译:使用聚合酶链反应从粟酒裂殖酵母中分离出编码巯基转移酶的基因组DNA。通过Southern杂交确认扩增的DNA片段,用HindIII和BamHI完全消化,然后连接到酵母-大肠杆菌穿梭载体pRS316中,得到质粒pEH1。将质粒pEH1的插入片段转移到多拷贝载体YEp357中以产生质粒pYEH1。所确定的核苷酸序列具有由四个外显子和三个内含子组成的开放阅读框,其编码101个氨基酸的多肽,分子量为11 261 Da。在含有质粒pYEH1的酿酒酵母中,巯基转移酶活性分别提高了1.6倍,在含有质粒pEH1和pYEH1的粟酒裂殖酵母中分别提高了1.8倍和2.7倍。将上游序列和编码N末端六个氨基酸的区域融合到穿梭载体YEp357R的无启动子β-半乳糖苷酶基因中,以产生融合质粒pYEHR1。发现由融合质粒合成β-半乳糖苷酶可被锌和生成NO的S-亚硝基-N-乙酰青霉胺增强。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号