Enomoto M, Stocker B A
Genetics. 1975 Dec;81(4):595-614. doi: 10.1093/genetics/81.4.595.
A fla mutant of E. coli K12 was given fla+ and H1-i by phage P1kc cotransduction from S. typhimurium, then made Fla- by transduction of ah1 from S. typhimurium. Motile clones expressing a Salmonella phase-2 antigen, e,n,x or 1,2, were obtained from the K12 i ah1 (therefore Fla-) line by P1kc transduction of flagellin-specifying genes, H2-e,n,x or H2-1,2, from Salmonella donors. Of eighteen such transductants sixteen failed to show phase variation, and on transduction back to Salmonella each structural gene for a phase-2 flagellin (or at least for its antigenically determinant part) now behaved as an allele of H1, presumably in consequence of incorporation in the hag region of the K12 recipient, in place of H1-i ah1. The e,n,x- and 1,2-specifying genes were shown to have been integrated in the K12 chromosome without the linked H1-repressor gene or the adjacent vh2 gene (controlling rate of phase-variation) and they responded to the repressing activity of an H2 allele elsewhere in the cell, in this respect resembling H1 alleles of Salmonella or hag alleles of E. coli. Two K12 e,n,x transductants had flagellin-specifying genes which when transduced back to Salmonella were integrated at H2; they are inferred to have resulted from integration of H2-e,n,x in the K12 chromosome elsewhere than the hag region. These two clones showed phase variation, between a Fla+ phase, with antigen e,n,x, and a Fla- phase (with e,n,x determinant in the nonactive state and the determinant of antigen i inactivated by ah1). The two integrated e,n,x genes when in the "active" state retained the ability to repress expression of exogenote H1 alleles, which indicates that the closely linked H1-repressor gene also was integrated. One of the two exceptional transductants derived its e,n,x gene from a Salmonella donor with the linked vh2- gene, which in Salmonella almost entirely prevents change of phase, and transduction of this e,n,x gene back to Salmonella recipients proved that vh2- had been incorporated into the E. coli chromosome along with the e,n,x determinant and the H1-repressor gene. The high frequency of change of phase (Fla+ in equilibrium Fla-) in the K12 e,n,x vh2- transductant concerned suggests that vh2- fails to prevent frequent change of state of the phase-determined part of H2 when vh2- and H2 are incorporated in the E. coli chromosome.
通过噬菌体P1kc从鼠伤寒沙门氏菌共转导,给大肠杆菌K12的一个fla突变体赋予了fla⁺和H1⁻i,然后通过从鼠伤寒沙门氏菌转导ah1使其变为Fla⁻。通过从沙门氏菌供体P1kc转导鞭毛蛋白指定基因H2 - e,n,x或H2 - 1,2,从K12 i ah1(因此是Fla⁻)品系中获得了表达沙门氏菌2相抗原e,n,x或1,2的运动性克隆。在这18个这样的转导子中,有16个没有表现出相变异,并且当转导回沙门氏菌时,每个2相鞭毛蛋白的结构基因(或至少其抗原决定部分)现在表现为H1的等位基因,大概是由于整合到了K12受体的hag区域,取代了H1 - i ah1。已表明e,n,x和1,2指定基因已整合到K12染色体中,没有与H1抑制基因或相邻的vh2基因(控制相变异速率)相连,并且它们对细胞中其他位置的H2等位基因的抑制活性有反应,在这方面类似于沙门氏菌的H1等位基因或大肠杆菌的hag等位基因。两个K12 e,n,x转导子具有鞭毛蛋白指定基因,当转导回沙门氏菌时,这些基因在H2处整合;推测它们是由于H2 - e,n,x在K12染色体上hag区域以外的其他位置整合所致。这两个克隆表现出相变异,在具有抗原e,n,x的Fla⁺相和Fla⁻相之间(在非活性状态下具有e,n,x决定簇,并且抗原i的决定簇被ah1灭活)。当处于“活性”状态时,这两个整合的e,n,x基因保留了抑制外基因H1等位基因表达的能力,这表明紧密相连的H1抑制基因也已整合。这两个异常转导子之一的e,n,x基因来自带有相连vh2⁻基因的沙门氏菌供体,在沙门氏菌中vh2⁻几乎完全阻止相的改变,并且将这个e,n,x基因转导回沙门氏菌受体证明vh2⁻已与e,n,x决定簇和H1抑制基因一起整合到大肠杆菌染色体中。所涉及的K12 e,n,x vh2⁻转导子中相(Fla⁺与Fla⁻平衡)的高频率变化表明,当vh2⁻和H2整合到大肠杆菌染色体中时,vh2⁻无法阻止H2相决定部分状态的频繁改变。