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Identification of Escherichia coli region III flagellar gene products and description of two new flagellar genes.

机译:鉴定大肠杆菌III区鞭毛基因产物并描述两个新鞭毛基因。

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Region III flagellar genes in Escherichia coli are involved with the assembly and rotation of the flagella, as well as taxis. We subcloned the flaB operon from a lambda fla transducing phage onto plasmid pMK2004. Two additional genes were found at the flaB locus, and we subdivided the flaB gene into flaB1, flaBII, and flaBIII. The cheY suppressor mutations which have previously been mapped to flaB were further localized to flaB11 (Parkinson et al., J. Bacteriol. 155:265-274, 1983). Until now, gene product identification has not been possible for these genes because of their low levels of gene expression. Overexpression of the flagellar genes was accomplished by placing the flaB operon under the control of the lacUV5 or tac promoters. Plasmid-encoded proteins were examined in a minicell expression system. By correlating various deletions and insertions in the flaB operon with the ability to complement specific flagellar mutants and code for polypeptides, we made the following gene product assignments: flaB 1, 60 kilodaltons; flaB 11, 38 kilodaltons; flaB111, 28 kilodaltons; flaC, 56 kilodaltons; fla0, 16 kilodaltons; and flaE, 54 kilodaltons.
机译:大肠杆菌中的III区鞭毛基因与鞭毛以及滑行的组装和旋转有关。我们从λfla转导噬菌体到质粒pMK2004亚克隆了flaB操纵子。在flaB基因座处发现了两个其他基因,我们将flaB基因细分为flaB1,flaBII和flaBIII。先前已定位到flaB的cheY抑制剂突变进一步定位于flaB11(Parkinson等,细菌学杂志(J.Bacteriol。)155:265-274,1983)。到目前为止,由于这些基因的基因表达水平较低,因此尚无法鉴定这些基因的基因产物。通过将flaB操纵子置于lacUV5或tac启动子的控制下,可以完成鞭毛基因的过表达。在小细胞表达系统中检查质粒编码的蛋白。通过将flaB操纵子中的各种缺失和插入与补充特定鞭毛突变体并编码多肽的能力相关联,我们进行了以下基因产物分配:flaB 1,60千道尔顿; 11、38道尔顿; flaB111,28道尔顿; flaC,56千道尔顿; fla0,16千道尔顿;和flE,54道尔顿。

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