Suppr超能文献

产肠毒素大肠杆菌的定居因子抗原II(CFA/II):CS3决定簇的分子克隆

Colonization factor antigen II (CFA/II) of enterotoxigenic Escherichia coli: molecular cloning of the CS3 determinant.

作者信息

Manning P A, Timmis K N, Stevenson G

出版信息

Mol Gen Genet. 1985;200(2):322-7. doi: 10.1007/BF00425443.

Abstract

The genes for the cell surface associated antigen CS3, produced by CFA/II type enterotoxigenic Escherichia coli, have been cloned in the plasmid vector pBR322 to produce a family of recombinant plasmids. These plasmids contain a series of HindIII fragments of which a fragment of 4.6 kb is common to all those expressing CS3. One of these plasmids, pPM474, has been subjected to mutagenesis with Tn1725 and deletions generated using Bal31. This has defined a minimum region of 3.75 kb necessary for the production of CS3 on the cell surface and implying genetic complexity as has been observed with other fimbrial antigens. Analysis of the plasmid encoded proteins in E. coli K-12 minicells has confirmed this complexity.

摘要

由CFA/II型产肠毒素大肠杆菌产生的细胞表面相关抗原CS3的基因已被克隆到质粒载体pBR322中,以产生一系列重组质粒。这些质粒含有一系列HindIII片段,其中4.6 kb的片段对于所有表达CS3的质粒来说是共同的。其中一个质粒pPM474已用Tn1725进行诱变,并使用Bal31产生缺失。这确定了在细胞表面产生CS3所需的最小区域为3.75 kb,这意味着其遗传复杂性与其他菌毛抗原中观察到的情况一样。对大肠杆菌K-12微小细胞中质粒编码蛋白的分析证实了这种复杂性。

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