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介导对哺乳动物细胞甘露糖抗性黏附的大肠杆菌SS142菌毛的特性

Properties of pili from Escherichia coli SS142 that mediate mannose-resistant adhesion to mammalian cells.

作者信息

Mett H, Kloetzlen L, Vosbeck K

出版信息

J Bacteriol. 1983 Feb;153(2):1038-44. doi: 10.1128/jb.153.2.1038-1044.1983.

Abstract

We isolated pili from Escherichia coli SS142. These pili had a diameter of 6 nm and an average length of 400 nm. They were composed of subunits with a molecular weight of 18,000. Their amino acid composition was determined; methionine and proline were not detected. The isolated pili retained mannose-resistant hemagglutinating activity. Proteolytic digestion and glutaraldehyde fixation led to partial or complete loss of the hemagglutinating activity of the pili without causing any detectable damage to their supramolecular structure, which was only disintegrated by treatment with hot sodium dodecyl sulfate. The hemagglutinating activity of E. coli SS142 was inhibited by the glycoproteins fetuin and Tamm-Horsfall protein, as well as by the glycolipids phytyl lactoside, dansyl-sphingosine lactoside, and digalactosyl diglyceride. Isolated pili inhibited the adhesion of the homologous strain E. coli SS142 to Intestine 407 cell monolayers, but did not inhibit the adhesion of E. coli strain B-413, B-506, or 2699. This indicates that E. coli SS142 binds to a receptor different from those recognized by the other strains and that mannose-resistant adhesion to tissue culture cells can be classified into different subtypes.

摘要

我们从大肠杆菌SS142中分离出菌毛。这些菌毛直径为6纳米,平均长度为400纳米。它们由分子量为18,000的亚基组成。测定了它们的氨基酸组成;未检测到甲硫氨酸和脯氨酸。分离出的菌毛保留了抗甘露糖血凝活性。蛋白水解消化和戊二醛固定导致菌毛的血凝活性部分或完全丧失,而对其超分子结构未造成任何可检测到的损伤,只有用热十二烷基硫酸钠处理才会使其解体。大肠杆菌SS142的血凝活性受到糖蛋白胎球蛋白和Tamm-Horsfall蛋白以及糖脂植基乳糖苷、丹磺酰鞘氨醇乳糖苷和二半乳糖基甘油二酯的抑制。分离出的菌毛抑制同源菌株大肠杆菌SS142对肠407细胞单层的黏附,但不抑制大肠杆菌B-413、B-506或2699菌株的黏附。这表明大肠杆菌SS142与其他菌株识别的受体不同,并且对组织培养细胞的抗甘露糖黏附可分为不同的亚型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af01/221728/dc7f2bf33422/jbacter00249-0470-a.jpg

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