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首页> 外文期刊>Molecular Microbiology >CAPSULAR POLYSACCHARIDE SYNTHESIS IN STREPTOCOCCUS PNEUMONIAE SEROTYPE 14 - MOLECULAR ANALYSIS OF THE COMPLETE CPS LOCUS AND IDENTIFICATION OF GENES ENCODING GLYCOSYLTRANSFERASES REQUIRED FOR THE BIOSYNTHESIS OF THE TETRASACCHARIDE SUBUNIT
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CAPSULAR POLYSACCHARIDE SYNTHESIS IN STREPTOCOCCUS PNEUMONIAE SEROTYPE 14 - MOLECULAR ANALYSIS OF THE COMPLETE CPS LOCUS AND IDENTIFICATION OF GENES ENCODING GLYCOSYLTRANSFERASES REQUIRED FOR THE BIOSYNTHESIS OF THE TETRASACCHARIDE SUBUNIT

机译:肺炎链球菌血清型14中的荚膜多糖合成-完整CPS分子的分子分析和编码糖基亚基生物合成所需的糖基转移酶的基因的鉴定

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摘要

We have reported previously on seven genes (cps14B-H) of Streptococcus pneumoniae serotype 14, which are part of the type 14 capsular polysaccharide synthesis (cps14) locus, This study describes the cloning and sequencing of the remaining part of the cps14 locus. The entire cps14 gene cluster consists of 12 open reading genes (cps14A to cps14L), which appear to be arranged as a single transcriptional unit, The flanking regions of the cps14 locus contain vestiges of insertion elements. Moreover, a 115-bp-long repeated DNA element, which is also present in several other intergenic regions on the pneumococcal chromosome, has been identified upstream of cps14A. All 12 open reading frames (ORFs) were inactivated by the insertion of a tetracycline resistance cassette. The cps14A to cps14J and cps14L mutants were unencapsulated, whereas only a limited amount of capsular polysaccharide was expressed by a cps14K insertion mutant. Comparison with DNA and protein sequences available in databases allowed us to predict functions for four out of the five new cps14 gene products, The biosynthetic function of Cps14I was determined experimentally by analysis of intermediates in the synthesis of the type 14 tetrasaccharide subunit, catalysed by membrane preparations of Escherichia coli expressing pneumococcal glycosyltransferases. [References: 46]
机译:我们以前曾报道过肺炎链球菌血清型14的七个基因(cps14B-H),它们是14型荚膜多糖合成(cps14)基因座的一部分,这项研究描述了cps14基因座其余部分的克隆和测序。整个cps14基因簇由12个开放阅读基因(cps14A至cps14L)组成,这些基因似乎排列为单个转录单位。cps14基因座的侧翼区域包含插入元件的痕迹。此外,已经在cps14A的上游发现了一个115 bp长的重复DNA元件,该元件也存在于肺炎球菌染色体上的其他几个基因间区域。通过插入四环素抗性盒使所有12个开放阅读框(ORF)失活。 cps14A到cps14J和cps14L突变体未封装,而cps14K插入突变体仅表达有限量的荚膜多糖。通过与数据库中可用的DNA和蛋白质序列进行比较,我们可以预测五种新的cps14基因产物中四种的功能。通过分析膜催化的14型四糖亚基合成中的中间体,实验确定了Cps14I的生物合成功能。表达肺炎球菌糖基转移酶的大肠杆菌的制剂。 [参考:46]

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