Fortin C, Marquis C, Nester E W, Dion P
Département de Phytologie, Faculté des Sciences de l'Agriculture et de l'Alimentation, Université Laval, Québec, Canada.
J Bacteriol. 1993 Aug;175(15):4790-9. doi: 10.1128/jb.175.15.4790-4799.1993.
Agrobacterium tumefaciens C58F is a variant of strain C58 which generates a high proportion of avirulent mutants in the presence of the virulence (vir) gene inducer acetosyringone. These mutants are altered in the Ti plasmid and do not respond to the acetosyringone signal (C. Fortin, E. W. Nester, and P. Dion, J. Bacteriol. 174:5676-5685, 1992). The physical organization of the Ti plasmid was compared in strain C58 and its variant. One feature distinguishing pTiC58F from its parent plasmid was the presence of the insertion element IS426. Three copies of this element were detected in the strain C58 chromosome, whereas two additional copies were found in strain C58F, including one copy in the Ti plasmid. This particular copy of IS426 was associated with the region of arginine and nopaline catabolism of pTiC58F. Most of the avirulent mutants recovered following growth of strain C58F in the presence of acetosyringone were complemented by clones carrying either virA or virG. Element IS426 was no longer found in the arginine and nopaline catabolism region of the Ti plasmids from the virA and virG mutants, but it resided in the particular KpnI fragment containing the modified vir locus. Behavior of a strain C58F derivative, which was inactivated in a chromosomal component required for the response to acetosyringone, was consistent with the possibility that vir gene induction is essential to the massive production of avirulent mutants.
根癌土壤杆菌C58F是C58菌株的一个变体,在毒性(vir)基因诱导剂乙酰丁香酮存在的情况下会产生高比例的无毒突变体。这些突变体在Ti质粒中发生了改变,并且对乙酰丁香酮信号没有反应(C. 福尔坦、E. W. 内斯特和P. 迪翁,《细菌学杂志》174:5676 - 5685,1992年)。对C58菌株及其变体中的Ti质粒的物理结构进行了比较。区分pTiC58F与其亲本质粒的一个特征是插入元件IS426的存在。在C58菌株染色体中检测到该元件的三个拷贝,而在C58F菌株中发现了另外两个拷贝,包括Ti质粒中的一个拷贝。IS426的这个特定拷贝与pTiC58F的精氨酸和胭脂碱分解代谢区域相关。在乙酰丁香酮存在的情况下C58F菌株生长后获得的大多数无毒突变体可被携带virA或virG的克隆互补。在来自virA和virG突变体的Ti质粒的精氨酸和胭脂碱分解代谢区域中不再发现元件IS426,但它存在于包含修饰的vir位点的特定KpnI片段中。C58F菌株衍生物的行为,该衍生物在对乙酰丁香酮反应所需的染色体组分中失活,这与vir基因诱导对于大量产生无毒突变体至关重要的可能性是一致的。