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肺炎链球菌中荚膜多糖合成基因簇的多样性

Diversity of capsular polysaccharide synthesis gene clusters in Streptococcus pneumoniae.

作者信息

Kolkman M A, van der Zeijst B A, Nuijten P J

机构信息

Department of Bacteriology, Institute of Infectious Diseases and Immunology, School of Veterinary Medicine, Universiteit Utrecht, P.O. Box 80.165, 3508 TD Utrecht, The Netherlands.

出版信息

J Biochem. 1998 May;123(5):937-45. doi: 10.1093/oxfordjournals.jbchem.a022028.

Abstract

Streptococcus pneumoniae comprises 90 serotypes, each one having its own specific polysaccharide capsule. In order to explore the diversity of capsular polysaccharide synthesis (cps) gene clusters in S. pneumoniae, we performed cross-hybridizations between the 12 cps genes of S. pneumoniae serotype 14 and chromosomal DNA of 26 strains comprising 26 different capsule types. Large variations in the hybridization patterns were observed. The genes cps14A to cps14D are conserved in most serotypes. Sequences homologous to cps14I to cps14L were only observed in the four types of serogroup 15, which all have a capsule structure similar to that of type 14. By using a cps14E knock-out construct, cpsE mutants of the pneumococcal types 9N, 13, and 15B were obtained. These mutants were unencapsulated and showed reduced glycosyltransferase activity, indicating that the pneumococcal types 9N, 13, and 15B express a glucosyl-1-phosphate transferase which is homologous to Cps14E. Glycosyltransferase assays showed that among 21 pneumococcal types which contain glucose in the core of their capsule polysaccharide, 19 types express glucosyl-1-phosphate transferase activity. However, not all of these types hybridized strongly with Cps14E, the type 14 glucosyl-1-phosphate transferase gene. Thus, pneumococci possess glucosyltransferase genes distinct from cps14E, but encoding enzymes with identical activity. All serotypes which synthesized lipid-linked lactose intermediates in glycosyltransferase activity assays (type 11B, 13, 15F, 15A, 15B, 15C) hybridized with cps14G. This gene encodes a galactosyltransferase which catalyzes the addition of 1,4-linked beta-galactose to lipid-linked glucose. The cps14G homologues in type 11B, 13, 15F, 15A, 15B, and 15C may encode a similar beta-galactosyltransferase activity as cps14G in type 14.

摘要

肺炎链球菌有90种血清型,每种血清型都有其特定的多糖荚膜。为了探究肺炎链球菌中荚膜多糖合成(cps)基因簇的多样性,我们对肺炎链球菌14型的12个cps基因与包含26种不同荚膜类型的26株菌株的染色体DNA进行了交叉杂交。观察到杂交模式存在很大差异。基因cps14A至cps14D在大多数血清型中是保守的。仅在血清群15的四种类型中观察到与cps14I至cps14L同源的序列,这四种类型的荚膜结构均与14型相似。通过使用cps14E基因敲除构建体,获得了肺炎球菌9N型、13型和15B型的cpsE突变体。这些突变体无荚膜,且糖基转移酶活性降低,这表明肺炎球菌9N型、13型和15B型表达一种与Cps14E同源的葡糖基-1-磷酸转移酶。糖基转移酶测定表明,在其荚膜多糖核心中含有葡萄糖的21种肺炎球菌类型中,有19种具有葡糖基-1-磷酸转移酶活性。然而,并非所有这些类型都与14型葡糖基-1-磷酸转移酶基因Cps14E强烈杂交。因此,肺炎球菌拥有与cps14E不同但编码具有相同活性的酶的葡糖基转移酶基因。在糖基转移酶活性测定中合成脂质连接乳糖中间体的所有血清型(11B型、13型、15F型、15A型、15B型、15C型)均与cps14G杂交。该基因编码一种半乳糖基转移酶,可催化将1,4-连接的β-半乳糖添加到脂质连接的葡萄糖上。11B型、13型、15F型、15A型、15B型和15C型中的cps14G同源物可能编码与14型中的cps14G相似的β-半乳糖基转移酶活性。

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