Bartlett D H, Matsumura P
J Bacteriol. 1984 Nov;160(2):577-85. doi: 10.1128/jb.160.2.577-585.1984.
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.
大肠杆菌中的III区鞭毛基因与鞭毛的组装、旋转以及趋化性有关。我们将来自λfla转导噬菌体的flaB操纵子亚克隆到质粒pMK2004上。在flaB位点发现了另外两个基因,我们将flaB基因细分为flaB1、flaBII和flaBIII。先前已定位到flaB的cheY抑制突变进一步定位到flaB11(帕金森等人,《细菌学杂志》155:265 - 274,1983)。到目前为止,由于这些基因的表达水平较低,还无法对其基因产物进行鉴定。通过将flaB操纵子置于lacUV5或tac启动子的控制之下,实现了鞭毛基因的过表达。在一个小细胞表达系统中检测了质粒编码的蛋白质。通过将flaB操纵子中的各种缺失和插入与互补特定鞭毛突变体的能力以及编码多肽的能力相关联,我们进行了以下基因产物的分配:flaB 1,60千道尔顿;flaB 11,38千道尔顿;flaB111,28千道尔顿;flaC,56千道尔顿;fla0,16千道尔顿;以及flaE,54千道尔顿。