Klapwijk P M, Schilperoort R A
J Bacteriol. 1979 Aug;139(2):424-31. doi: 10.1128/jb.139.2.424-431.1979.
The regulatory system that controls the expression of the Ti plasmid-borne octopine degradation (uad) and transfer (tra) genes in Agrobacterium tumefaciens was studied. A deletion mutant derived from the cointegrate plasmid R702::Ti-B6S3 was isolated, which was compatible with a wild-type Ti plasmid and which had retained the uad genes. By means of this mutant plasmid pAL116, it was possible to make cells diploid for the uad genes. pAL116 was introduced into Rec- strains that contained different types of regulation mutants for the uad and tra genes. The repression pattern that was found in this complementation analysis indicated that the uad and tra operons are controlled by a common repressor system. Several results indicated that there may be additional transcriptional relations between both operons. The corresponding genes of the non-tumorigenic octopine plasmid pAt-AG60 appeared to be controlled by a repressor related to that of the octopine Ti plasmid.
对控制根癌土壤杆菌中Ti质粒携带的章鱼碱降解(uad)和转移(tra)基因表达的调控系统进行了研究。分离得到了一个源自共整合质粒R702::Ti-B6S3的缺失突变体,它与野生型Ti质粒相容并保留了uad基因。借助该突变体质粒pAL116,有可能使细胞对于uad基因成为二倍体。将pAL116导入含有不同类型uad和tra基因调控突变体的Rec-菌株中。在这种互补分析中发现的阻遏模式表明,uad和tra操纵子受一个共同的阻遏系统控制。几个结果表明,两个操纵子之间可能存在其他转录关系。非致瘤性章鱼碱质粒pAt-AG60的相应基因似乎受一种与章鱼碱Ti质粒的阻遏物相关的阻遏物控制。