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大肠杆菌的多糖荚膜:其大小、结构及合成位点的显微镜研究

Polysaccharide capsule of Escherichia coli: microscope study of its size, structure, and sites of synthesis.

作者信息

Bayer M E, Thurow H

出版信息

J Bacteriol. 1977 May;130(2):911-36. doi: 10.1128/jb.130.2.911-936.1977.

Abstract

This report describes the structure, size, and shape of the uncollapsed polysaccharide capsule of Escherichia coli strain Bi 161/42 [O9:K29(A):H-], its ultrastructural preservation as well as the filamentous components of the isolated capsular material. In a temperature-sensitive mutant, sites were localized at which capsular polysaccharide is "exported" to the cell surface. The highly hydrated capsule of the wild-type cells was visible in the uncollapsed state after freeze-etching, whereas dehydration in greater than or equal to 50% acetone or alcohol caused the capsule to collapse into thick bundles. This was prevented by pretreatment of the cell with capsule-specific immunoglobulin G; the capsule appeared as a homogeneous layer of 250- to 300-nm thickness. The structural preservation depended on the concentration of the anti-capsular immunoglobulin G. Temperature-sensitive mutants, unable to produce capsular antigen at elevated temperatures, showed, 10 to 15 min after shift down to permissive temperature, polysaccharide strands with K29 specificity appearing at the cell surface at roughly 20 sites per cell; concomitantly, capsule-directed antibody started to agglutinate the bacteria. The sites at which the new antigen emerged were found in random distribution over the entire surface of the organism. Spreading of purified polysaccharide was achieved on air-water interfaces; after subsequent shadow casting with heavy metal, filamentous elements were observed with a smallest class of filaments measuring 250 nm in length and 3 to 6 nm in width. At one end these fibers revealed a knoblike structure of about 10-nm diameter. The slimelike polysaccharides from mutants produced filamentous bundles of greater than 100-microns length, with antigenic and phage-receptor properties indistinguishable from those of the wild-type K29 capsule antigen.

摘要

本报告描述了大肠杆菌菌株Bi 161/42 [O9:K29(A):H-]未塌陷的多糖荚膜的结构、大小和形状,其超微结构保存情况以及分离出的荚膜物质的丝状成分。在一个温度敏感突变体中,确定了荚膜多糖“输出”到细胞表面的位点。野生型细胞高度水合的荚膜在冷冻蚀刻后以未塌陷状态可见,而在大于或等于50%的丙酮或酒精中脱水会导致荚膜塌陷成粗束。用荚膜特异性免疫球蛋白G对细胞进行预处理可防止这种情况发生;荚膜呈现为厚度为250至300纳米的均匀层。结构保存取决于抗荚膜免疫球蛋白G的浓度。温度敏感突变体在高温下无法产生荚膜抗原,在转移到允许温度后10至15分钟,每个细胞表面大约20个位点出现具有K29特异性的多糖链;与此同时,针对荚膜的抗体开始使细菌凝集。新抗原出现的位点在生物体整个表面随机分布。在空气-水界面上实现了纯化多糖的铺展;随后用重金属进行投影后,观察到丝状成分,最小一类丝的长度为250纳米,宽度为3至6纳米。这些纤维的一端呈现出直径约为10纳米的球状结构。突变体产生的黏液样多糖形成了长度大于100微米的丝状束,其抗原性和噬菌体受体特性与野生型K29荚膜抗原无法区分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60a9/235297/2f9bd80e9c84/jbacter00306-0353-a.jpg

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