Characterization of the Agrobacterium octopine-cucumopine catabolic plasmid pAtAg67

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY
Marjolein J.G. Hooykaas, Shuai Shao , Paul J.J. Hooykaas
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引用次数: 1

Abstract

In addition to tumor-inducing agrobacteria, non-pathogenic strains are often isolated from crown gall tumors. Such non-pathogenic strains sometimes contain catabolic plasmids that allow them to take advantage of the opines produced in the tumors. Here we characterize for the first time an octopine catabolic plasmid, pAtAg67, which is derived from an Agrobacterium strain isolated from a grapevine tumor in Crete. By sequence analysis, we deduce that pAtAg67 enables its host to catabolize not only octopine, but also cucumopine and agrocinopine-like compounds. We found that a highly similar set of catabolic genes was present in the Ti plasmids of tumorigenic octopine-cucumopine grapevine strains such as pTiAg57. However, the catabolic genes in octopine-cucumopine Ti plasmids were interrupted by a T-DNA segment. As no T-DNA remnants, virulence genes or border repeats were found in pAtAg67, catabolic plasmid pAtAg67 does not appear to be a degenerate octopine-cucumopine Ti plasmid. In line, plasmid pAtAg67 was found to be compatible with incRh1 octopine Ti plasmids, but to be incompatible with the incRh2 agropine Ti plasmid pTiBo542, forming cointegrates by recombination in the homologous trb genes.

八爪农杆菌-黄瓜分解代谢质粒pAtAg67的鉴定
除了诱导肿瘤的农杆菌外,非致病性菌株也经常从冠瘿肿瘤中分离出来。这种非致病性菌株有时含有分解代谢质粒,使它们能够利用肿瘤中产生的嘌呤。在这里,我们首次描述了一种章鱼分解代谢质粒,pAtAg67,它来源于从克里特岛葡萄肿瘤中分离的一株农杆菌。通过序列分析,我们推断出pAtAg67不仅能使其宿主分解章鱼碱,还能分解黄瓜碱和农业碱样化合物。我们发现在致瘤性章鱼-黄瓜葡萄菌株(如pTiAg57)的Ti质粒中存在一组高度相似的分解代谢基因。然而,章鱼-黄瓜Ti质粒中的分解代谢基因被一个T-DNA片段打断。由于在pAtAg67中没有发现T-DNA残余物、毒力基因或边界重复序列,因此分解代谢质粒pAtAg67似乎不是退化的章鱼-黄瓜Ti质粒。结果表明,质粒pAtAg67与incRh1八肽Ti质粒相容,而与incRh2 agropine Ti质粒pTiBo542不相容,在同源trb基因中重组形成共整合体。
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来源期刊
Plasmid
Plasmid 生物-遗传学
CiteScore
4.70
自引率
3.80%
发文量
21
审稿时长
53 days
期刊介绍: Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.
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