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首页> 外文期刊>Infection and immunity >Molecular analysis of lipooligosaccharide biosynthesis in Neisseria gonorrhoeae.
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Molecular analysis of lipooligosaccharide biosynthesis in Neisseria gonorrhoeae.

机译:淋病奈瑟氏球菌中脂寡糖生物合成的分子分析。

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A HindIII gene bank of Neisseria gonorrhoeae MUG116 was constructed in the cosmid vector pHC79. A cosmid (pSY81) was isolated that was able to convert N. gonorrhoeae FA5100 to reactivity with monoclonal antibody (MAb) 2-1-L8. Several MAb-reactive transformants were isolated and characterized with respect to lipooligosaccharide (LOS) production as analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, their ability to react with two other LOS-specific MAbs (3F11 and O6B4), and Southern blot analysis. Escherichia coli containing the clone had altered lipopolysaccharide expression as determined by electrophoretic analysis; however, no reactivity was seen with gonococcus-specific MAbs. The introduction of pSY81 into FA5100 had a pleiomorphic effect, giving rise to transformants having the full parental phenotype or transformants lacking reactivity to a combination of LOS-specific MAbs. Southern blot analysis indicated that the LOS biosynthetic mutation in FA5100 was not due to chromosomal rearrangement or large deletions.
机译:在粘粒载体pHC79中构建了淋病奈瑟氏球菌MUG116的HindIII基因库。分离出能够将淋病奈瑟氏球菌FA5100转化为与单克隆抗体(MAb)2-1-L8具有反应性的粘粒(pSY81)。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳,与其他两种LOS特异性MAb(3F11和O6B4)反应的能力以及Southern印迹分析,分离并表征了几种MAb反应性转化体,并描述了脂寡糖(LOS)的产生。如电泳分析所示,含有该克隆的大肠杆菌改变了脂多糖的表达。但是,没有针对性针对特定的球菌的单克隆抗体。将pSY81引入FA5100具有多态性作用,产生具有完全亲本表型的转化子或对LOS特异性MAb的组合缺乏反应性的转化子。 Southern印迹分析表明,FA5100中的LOS生物合成突变不是由于染色体重排或大的缺失。

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