Beutin L, Manning P A, Achtman M, Willetts N
J Bacteriol. 1981 Feb;145(2):840-4. doi: 10.1128/jb.145.2.840-844.1981.
The mechanisms whereby mutations in Escherichia coli K-12 genes sfrA and sfrB reduce expression of the transfer functions of sex factor F have been examined by assaying the levels of tra messenger ribonucleic acid and of tra proteins. The sfrA product was necessary for efficient transcription of the control gene traJ and, directly or indirectly, for transcription of the traY leads to Z operon. In the absence of sfrA, reduced levels of the traJ and traT proteins were observed in the outer membrane. The sfrB product was needed to prevent premature transcription at one or more rho-dependent termination sites. sfrB mutations also reduced synthesis of full-length lipopolysaccharide molecules, of several chromosomally determined outer membrane proteins, and of functional flagella. Thus, the sfrB product may act as an antiterminator in transcription of several operons encording cell envelope components.
通过检测tra信使核糖核酸和tra蛋白的水平,研究了大肠杆菌K-12基因sfrA和sfrB中的突变降低性因子F转移功能表达的机制。sfrA产物对于控制基因traJ的有效转录是必需的,并且直接或间接地对于traY到Z操纵子的转录是必需的。在没有sfrA的情况下,在外膜中观察到traJ和traT蛋白水平降低。sfrB产物是防止在一个或多个ρ依赖性终止位点过早转录所必需的。sfrB突变还减少了全长脂多糖分子、几种染色体决定的外膜蛋白和功能性鞭毛的合成。因此,sfrB产物可能在编码细胞包膜成分的几个操纵子的转录中充当抗终止子。