Scheeren-Groot E P, Rodenburg K W, den Dulk-Ras A, Turk S C, Hooykaas P J
Institute of Molecular Plant Sciences, Clusius Laboratory, Leiden University, The Netherlands.
J Bacteriol. 1994 Nov;176(21):6418-26. doi: 10.1128/jb.176.21.6418-6426.1994.
To find VirG proteins with altered properties, the virG gene was mutagenized. Random chemical mutagenesis of single-stranded DNA containing the Agrobacterium tumefaciens virG gene led with high frequency to the inactivation of the gene. Sequence analysis showed that 29% of the mutants contained a virG gene with one single-base-pair substitution somewhere in the open reading frame. Thirty-nine different mutations that rendered the VirG protein inactive were mapped. Besides these inactive mutants, two mutants in which the vir genes were active even in the absence of acetosyringone were found on indicator plates. A VirG protein with an N54D substitution turned out to be able to induce a virB-lacZ reporter gene to a high level even in the absence of the inducer acetosyringone. A VirG protein with an I77V substitution exhibited almost no induction in the absence of acetosyringone but showed a maximum induction level already at low concentrations of acetosyringone.
为了找到具有改变性质的VirG蛋白,对virG基因进行了诱变。对含有根癌农杆菌virG基因的单链DNA进行随机化学诱变,高频导致该基因失活。序列分析表明,29%的突变体在开放阅读框的某处含有一个具有单碱基对替换的virG基因。绘制了39个使VirG蛋白失活的不同突变位点。除了这些无活性突变体,在指示平板上还发现了两个即使在没有乙酰丁香酮的情况下vir基因仍具有活性的突变体。结果表明,具有N54D替换的VirG蛋白即使在没有诱导剂乙酰丁香酮的情况下也能高水平诱导virB-lacZ报告基因。具有I77V替换的VirG蛋白在没有乙酰丁香酮的情况下几乎没有诱导作用,但在低浓度乙酰丁香酮时就显示出最大诱导水平。