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大肠杆菌K1荚膜生物合成基因的克隆与分析:与B群脑膜炎奈瑟菌DNA序列缺乏同源性。

Cloning and analysis of the K1 capsule biosynthesis genes of Escherichia coli: lack of homology with Neisseria meningitidis group B DNA sequences.

作者信息

Echarti C, Hirschel B, Boulnois G J, Varley J M, Waldvogel F, Timmis K N

出版信息

Infect Immun. 1983 Jul;41(1):54-60. doi: 10.1128/iai.41.1.54-60.1983.

Abstract

Genes coding for production of the K1 polysaccharide capsule of Escherichia coli have been cloned. Complementation, insertion, and deletion analyses were used to localize the K1 genes and demonstrated that a minimum of 9 kilobases of DNA split into at least two gene blocks is involved in synthesis and assembly of the capsule. One of the gene blocks is responsible for biosynthesis of the polysaccharide, and the other is responsible for extracellular appearance of capsular material. Using cloned K1 genes as probes in Southern blot experiments, we detected homology to DNA from strains of E. coli capsular types K92, K7, and K100. In contrast, no homology was apparent between K1 genes and DNA from meningococcus group B, although the K1 and group B capsules are chemically and immunologically identical.

摘要

编码大肠杆菌K1多糖荚膜产生的基因已被克隆。通过互补、插入和缺失分析来定位K1基因,结果表明至少9千碱基的DNA分成至少两个基因块参与荚膜的合成和组装。其中一个基因块负责多糖的生物合成,另一个负责荚膜物质的细胞外呈现。在Southern印迹实验中使用克隆的K1基因作为探针,我们检测到与大肠杆菌荚膜类型K92、K7和K100菌株的DNA具有同源性。相比之下,尽管K1和B群脑膜炎球菌的荚膜在化学和免疫方面相同,但K1基因与B群脑膜炎球菌的DNA之间没有明显的同源性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdea/264742/1363063c7bf4/iai00136-0066-a.jpg

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