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Identification of additional genes required for O-antigen biosynthesis in Vibrio cholerae O1.

机译:鉴定霍乱弧菌O1中O抗原生物合成所需的其他基因。

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The cloning and expression of the genes encoding the Vibrio cholerae O1 lipopolysaccharide O antigen in a heterologous host have been described previously (P. A. Manning, M. W. Heuzenroeder, J. Yeadon, D. I. Leavesley, P. R. Reeves, and D. Rowley, Infect. Immun. 53:272-277, 1986). It was thus assumed that all the genes required for O-antigen expression were located on a 20-kb SacI restriction fragment. We present evidence for a number of other as yet undescribed genes that are essential for O-antigen biosynthesis in V. cholerae O1 and that these genes are somehow complemented in Escherichia coli K-12. The two genes termed Vibrio cholerae rfbV and rfbU are transcribed in the opposite orientation from the rest of the rfb operon, whereas the galE dehydratase and rfbP (Salmonella enterica) homologs, designated ORF35x7 and rfbW, respectively, are transcribed in the same orientation. The evidence presented here, using chromosomal insertion mutants, clearly shows that the three genes now designated rfbV, rfbU, and rfbW appear to be accessory rfb genes and are essential for O-antigen biosynthesis in V. cholerae but that ORF35x7 is not.
机译:先前已经描述了在异源宿主中编码霍乱弧菌O1脂多糖O抗原的基因的克隆和表达(PA Manning,MW Heuzenroeder,J. Yeadon,DI Leavesley,PR Reeves和D.Rowley,Infect。Immun。53 :272-277,1986)。因此,假定O-抗原表达所需的所有基因都位于20kb SacI限制性片段上。我们提供了许多其他尚未证实的基因的证据,这些基因对于霍乱弧菌O1的O抗原生物合成至关重要,并且这些基因在某种程度上在大肠杆菌K-12中得到了补充。分别以与其余rfb操纵子相反的方向转录称为霍乱弧菌rfbV和rfbU的两个基因,而分别命名为ORF35x7和rfbW的galE脱水酶和rfbP(肠炎沙门氏菌)同系物以相同的方向转录。此处提供的使用染色体插入突变体的证据清楚地表明,现在命名为rfbV,rfbU和rfbW的三个基因似乎是辅助rfb基因,对于霍乱弧菌的O抗原生物合成必不可少,但ORF35x7不是。

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