Finke A, Bronner D, Nikolaev A V, Jann B, Jann K
Max-Planck-Institut für Immunobiologie, Freiburg, Federal Republic of Germany.
J Bacteriol. 1991 Jul;173(13):4088-94. doi: 10.1128/jb.173.13.4088-4094.1991.
Biosynthesis of the capsular K5 polysaccharide of Escherichia coli, which has the structure 4)-beta GlcA-1,4-alpha GlcNAc-(1, was studied with membrane preparations from an E. coli K5 wild-type strain and from a recombinant K-12 strain expressing the K5 capsule. Polymerization occurs at the inner face of the cytoplasmic membrane without the participation of lipid-linked oligosaccharides. The serological K5 specificity of the in vitro product was determined with a K5-specific monoclonal antibody in an antigen-binding assay. The K5 polysaccharide, as obtained from the membranes after an in vitro incubation, has 2-keto-3-deoxyoctulosonic acid as the reducing sugar, which indicates that the polysaccharide grows by chain elongation at the nonreducing end.
对大肠杆菌荚膜K5多糖(其结构为4)-β-D-葡萄糖醛酸-1,4-α-D-乙酰氨基葡萄糖-(1)的生物合成进行了研究,所用的膜制剂来自大肠杆菌K5野生型菌株和表达K5荚膜的重组K-12菌株。聚合反应发生在细胞质膜的内表面,无需脂连接寡糖的参与。通过抗原结合试验,用K5特异性单克隆抗体测定了体外产物的血清学K5特异性。体外孵育后从膜中获得的K5多糖,其还原糖为2-酮-3-脱氧辛糖酸,这表明多糖是在非还原端通过链延长而生长的。