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编码人肠产毒性大肠杆菌CS1菌毛主要亚基的基因。

Gene encoding the major subunit of CS1 pili of human enterotoxigenic Escherichia coli.

作者信息

Perez-Casal J, Swartley J S, Scott J R

机构信息

Department of Microbiology and Immunology, Emory University Health Sciences Center, Atlanta, Georgia 30322.

出版信息

Infect Immun. 1990 Nov;58(11):3594-600. doi: 10.1128/iai.58.11.3594-3600.1990.

Abstract

Some enterotoxigenic strains of Escherichia coli (ETEC) utilize the CS1 pilus for colonization of human intestinal epithelium. We have cloned the gene which encodes the major CS1 subunit and called it cooA (for coli surface antigen one). Hybridization showed that the ETEC strain from which it was cloned carried cooA on a plasmid different from the one encoding its positive regulator, rns. Based on the cooA DNA sequence, cleavage with signal peptidase would be expected to produce a mature protein of 15.2 kDa; a 16-kDa polypeptide that reacted with CS1-specific antiserum was observed on electrophoresis. At the protein level, there was 92% similarity and 55% identity between cooA and cfaB, the major colonization factor antigen I (CFA/I) antigen. However, CS1-specific antisera did not react with CfaB. No hybridization was seen between either of two different cooA probes and total DNA from ETEC strains expressing AFA-1, CFA/I, CS2, CS3, CS4, CS5, or CS6.

摘要

一些产肠毒素大肠杆菌(ETEC)菌株利用CS1菌毛定殖于人肠道上皮细胞。我们克隆了编码主要CS1亚基的基因,并将其命名为cooA(代表大肠杆菌表面抗原1)。杂交显示,克隆该基因所用的ETEC菌株携带cooA的质粒与编码其正调控因子rns的质粒不同。根据cooA的DNA序列,预期信号肽酶切割后会产生一个15.2 kDa的成熟蛋白;电泳时观察到一条与CS1特异性抗血清反应的16 kDa多肽。在蛋白质水平上,cooA与主要定殖因子抗原I(CFA/I)抗原cfaB之间有92%的相似性和55%的同一性。然而,CS1特异性抗血清不与CfaB反应。两种不同的cooA探针与表达AFA-1、CFA/I、CS2、CS3、CS4、CS5或CS6的ETEC菌株的总DNA之间均未观察到杂交。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab2/313703/e44baedda315/iai00059-0140-a.jpg

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