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噬菌体介导的解聚作用在大肠杆菌K36血清型荚膜多糖结构研究中的应用

The use of bacteriophage-mediated depolymerisation in the structural investigation of the capsular polysaccharide from Escherichia coli serotype K36.

作者信息

Parolis H, Parolis L A, Stanley S M

机构信息

School of Pharmaceutical Sciences, Rhodes University, Grahamstown, South Africa.

出版信息

Carbohydr Res. 1988 Apr 1;175(1):77-83. doi: 10.1016/0008-6215(88)80157-5.

Abstract

The structure of the repeating unit of the capsular polysaccharide from Escherichia coli serotype K36 has been established from the results of spectroscopic and chemical analyses of (a) P1, the tetrasaccharide obtained on depolymerisation of the polysaccharide with a bacteriophage-borne endo-galactosidase, (b) P1-alditol, and (c) the original polysaccharide. The repeating unit, which is identical to that reported for Klebsiella K57, has the following structure. (Formula: see text).

摘要

通过对以下物质进行光谱分析和化学分析,确定了大肠杆菌血清型K36荚膜多糖重复单元的结构:(a) P1,用噬菌体携带的内切半乳糖苷酶使多糖解聚得到的四糖;(b) P1-木糖醇;(c) 原始多糖。该重复单元与报道的肺炎克雷伯菌K57的重复单元相同,具有以下结构。(分子式:见正文)

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