Suppr超能文献

芽孢杆菌α-淀粉酶基因在酵母中的表达。

Expression of a Bacillus alpha-amylase gene in yeast.

作者信息

Pretorius I S, Laing E, Pretorius G H, Marmur J

机构信息

Department of Microbiology, University of Stellenbosch, South Africa.

出版信息

Curr Genet. 1988 Jul;14(1):1-8. doi: 10.1007/BF00405846.

Abstract

A recombinant plasmid, pSR11.3, containing the alpha-amylase gene (AMY) of Bacillus amyloliquefaciens was characterized and expressed in Bacillus subtilis. A 2.3 kilobase BamHI-BglII fragment carrying AMY was cloned into pBR322 (pEL322) and in both orientations into a multi-copy Escherichia coli-yeast shuttle vector YEp13 (pAM13) and expressed in E. coli HB101 and various Saccharomyces stains. We report on the successful secretion of an active bacterial enzyme in yeast without using yeast promoter and secretory signals. Enzyme production in B. subtilis 1A297(pSR11.3), E. coli HB101(pEL322) and Saccharomyces JM2773-15B(pAM13) transformants was measured as 125, 22 and 123 U/ml, respectively. The molecular weight of the purified alpha-amylase secreted by B. subtilis 1A297(pSR11.3) and Saccharomyces JM2773-15B-(pAM13) was estimated to be 55 kDa. The pH and temperature optima for the alpha-amylase activities of the transformants were 6.5 to 8.0 and 50 to 65 degrees C, respectively. Amylose hydrolysis profiles of the alpha-amylases secreted by B. subtilis 1A297(pSR11.3) and Saccharomyces JM2773-15B(pAM13) indicate effective meso-thermostable hydrolytic enzymes with maltotriose and maltose, respectively, as major end products.

摘要

对含有解淀粉芽孢杆菌α-淀粉酶基因(AMY)的重组质粒pSR11.3进行了表征,并在枯草芽孢杆菌中进行了表达。将携带AMY的2.3千碱基BamHI - BglII片段克隆到pBR322(pEL322)中,并以两种方向克隆到多拷贝大肠杆菌 - 酵母穿梭载体YEp13(pAM13)中,并在大肠杆菌HB101和各种酿酒酵母菌株中表达。我们报道了在不使用酵母启动子和分泌信号的情况下,在酵母中成功分泌活性细菌酶。枯草芽孢杆菌1A297(pSR11.3)、大肠杆菌HB101(pEL322)和酿酒酵母JM2773 - 15B(pAM13)转化体中的酶产量分别测定为125、22和123 U/ml。枯草芽孢杆菌1A297(pSR11.3)和酿酒酵母JM2773 - 15B - (pAM13)分泌的纯化α-淀粉酶的分子量估计为55 kDa。这些转化体α-淀粉酶活性的最适pH和温度分别为6.5至8.0和50至65℃。枯草芽孢杆菌1A297(pSR11.3)和酿酒酵母JM2773 - 15B(pAM13)分泌的α-淀粉酶的直链淀粉水解谱表明,它们分别是有效的中温稳定水解酶,主要终产物分别是麦芽三糖和麦芽糖。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验