Suppr超能文献

肉葡萄球菌TM300中Sau3AI限制与修饰基因的克隆、表达及特性分析

Cloning, expression and characterization of the Sau3AI restriction and modification genes in Staphylococcus carnosus TM300.

作者信息

Seeber S, Kessler C, Götz F

机构信息

Mikrobielle Genetik, Universität Tübingen, F.R.G.

出版信息

Gene. 1990 Sep 28;94(1):37-43. doi: 10.1016/0378-1119(90)90465-4.

Abstract

The genes encoding the restriction enzyme (ENase) and modification enzyme (MTase) of Staphylococcus aureus 3A (recognition sequence 5'-GATC-3') have been cloned in Staphylococcus carnosus TM300 using the vector pCA44. Clones carrying both genes were isolated from DNA libraries prepared with MboI + BamHI. The DNA region encoding M.Sau3AI was subcloned on a 3.66-kb EcoRV fragment in vector pT181mcs. Plasmids purified from the clones were resistant to digestion with Sau3AI, indicating that the sau3AIM gene was expressed and the product was functional in S. carnosus. Cell lysates of clones with both activities encoded on plasmid pSEM7, cut DNA with the same pattern as Sau3AI, showing that the sau3AIR gene was also expressed and the ENase was functional in S. carnosus. Sequence analysis shows that both genes are transcribed in the same direction and encode polypeptides with calculated Mrs of 56,477 for R.Sau3AI and 47,300 for M.Sau3AI. Efforts to clone one or both genes in Escherichia coli have so far failed.

摘要

金黄色葡萄球菌3A(识别序列5'-GATC-3')的限制性内切酶(ENase)和甲基化酶(MTase)编码基因已使用载体pCA44克隆到肉葡萄球菌TM300中。携带这两个基因的克隆是从用MboI + BamHI制备的DNA文库中分离出来的。编码M.Sau3AI的DNA区域亚克隆到载体pT181mcs中的一个3.66 kb的EcoRV片段上。从克隆中纯化的质粒对Sau3AI消化具有抗性,表明sau3AIM基因已表达且产物在肉葡萄球菌中具有功能。在质粒pSEM7上编码两种活性的克隆的细胞裂解物,切割DNA的模式与Sau3AI相同,表明sau3AIR基因也已表达且ENase在肉葡萄球菌中具有功能。序列分析表明,这两个基因都以相同方向转录,并且编码的多肽,R.Sau3AI的计算分子量为56,477,M.Sau3AI的计算分子量为47,300。到目前为止,在大肠杆菌中克隆一个或两个基因的努力均告失败。

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