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大肠杆菌K5抗原基因簇1区的分子分析:一个编码参与荚膜多糖细胞表面表达相关蛋白的区域。

Molecular analysis of region 1 of the Escherichia coli K5 antigen gene cluster: a region encoding proteins involved in cell surface expression of capsular polysaccharide.

作者信息

Pazzani C, Rosenow C, Boulnois G J, Bronner D, Jann K, Roberts I S

机构信息

Department of Microbiology, University of Leicester, England.

出版信息

J Bacteriol. 1993 Sep;175(18):5978-83. doi: 10.1128/jb.175.18.5978-5983.1993.

Abstract

The nucleotide sequence of region 1 of the K5 antigen gene cluster of Escherichia coli was determined. This region is postulated to encode functions which, at least in part, participate in translocation of polysaccharide across the periplasmic space and onto the cell surface. Analysis of the nucleotide sequence revealed five genes that encode proteins with predicted molecular masses of 75.7, 60.5, 44, 43, and 27 kDa. The 27-kDa protein was 70.7% homologous to the CMP-2-keto-3-deoxyoctulosonic acid synthetase enzyme encoded by the E. coli kdsB gene, indicating the presence of a structural gene for a similar enzyme within the region 1 operon. The 43-kDa protein was homologous to both the Ctrb and BexC proteins encoded by the Neisseria meningitidis and Haemophilus influenzae capsule gene clusters, respectively, indicating common stages in the expression of capsules in these gram-negative bacteria. However, no homology was detected between the 75.7, 60.5-, and 44-kDa proteins and any of the proteins so far described for the H. influenzae and N. meningitidis capsule gene clusters.

摘要

测定了大肠杆菌K5抗原基因簇区域1的核苷酸序列。推测该区域编码的功能至少部分参与多糖穿过周质空间并转运到细胞表面的过程。核苷酸序列分析揭示了五个基因,它们编码的蛋白质预测分子量分别为75.7、60.5、44、43和27 kDa。27 kDa的蛋白质与大肠杆菌kdsB基因编码的CMP-2-酮-3-脱氧辛酸合成酶有70.7%的同源性,表明区域1操纵子内存在一个类似酶的结构基因。43 kDa的蛋白质分别与脑膜炎奈瑟菌和流感嗜血杆菌荚膜基因簇编码的Ctrb和BexC蛋白同源,表明这些革兰氏阴性菌在荚膜表达上有共同阶段。然而,75.7、60.5和44 kDa的蛋白质与流感嗜血杆菌和脑膜炎奈瑟菌荚膜基因簇迄今描述的任何蛋白质之间均未检测到同源性。

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