Komeda Y
J Bacteriol. 1982 Apr;150(1):16-26. doi: 10.1128/jb.150.1.16-26.1982.
Previous studies have defined 29 genes necessary for synthesis of the Escherichia coli flagellar apparatus. This study analyzed the transcriptional control of flagellar genes, using Mu d (Apr lac) phage to generate flagellar mutants by insertion. These mutants contained operon fusions of flagellar genes to the lac genes of the Mu d phage and allowed the measurement of flagellar operon expression by detection of beta-galactosidase activity. These fusion mutants expressed the enzyme activity constitutively, and an autogenous regulation mechanism was not revealed. Lambda transducing phages carrying these chromosomal fla-lac fusions were also isolated and used to examine the effect of different fla mutations on expression of each flagellar operon. The results showed that flagellar operons are divided into six classes; (class 1) the flbB operon, which controls all of the other flagellar operons; (class 2) the flaU and flbC operons, which are controlled by the flbB operon gene products and are not required for the expression of other Fla operons; (class 3) the flbA, flaG, flaD, flaN, flaB, and flaA operons, which are under flbB operon control and are required for the expression of other fla operons; (class4) the flaZ operon, which is controlled by the gene products of the group 1 and 3 operons and is required for hag transcription; (class 5) the mocha and flaS operons, which are controlled by the gene products of the group 1 and 3 operons; and (class 6) the hag operon. These results are discussed with respect to the possible assembly sequence of the fla gene products.
先前的研究已经确定了大肠杆菌鞭毛装置合成所必需的29个基因。本研究利用Mu d(Apr lac)噬菌体通过插入来产生鞭毛突变体,从而分析鞭毛基因的转录控制。这些突变体包含鞭毛基因与Mu d噬菌体的lac基因的操纵子融合,并通过检测β-半乳糖苷酶活性来测量鞭毛操纵子的表达。这些融合突变体组成型地表达酶活性,未揭示出自生调节机制。还分离出携带这些染色体fla-lac融合的λ转导噬菌体,并用于研究不同fla突变对每个鞭毛操纵子表达的影响。结果表明,鞭毛操纵子分为六类;(第1类)flbB操纵子,它控制所有其他鞭毛操纵子;(第2类)flaU和flbC操纵子,它们受flbB操纵子基因产物的控制,并且其他Fla操纵子的表达不需要它们;(第3类)flbA、flaG、flaD、flaN、flaB和flaA操纵子,它们受flbB操纵子的控制,并且其他fla操纵子的表达需要它们;(第4类)flaZ操纵子,它受第1类和第3类操纵子基因产物的控制,并且是hag转录所必需的;(第5类)mocha和flaS操纵子,它们受第1类和第3类操纵子基因产物的控制;以及(第6类)hag操纵子。针对fla基因产物可能的组装顺序对这些结果进行了讨论。