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由直接重复元件介导的嗜碱假单胞菌NH9中3-氯苯甲酸酯分解代谢质粒的重组

Recombination of a 3-chlorobenzoate catabolic plasmid from Alcaligenes eutrophus NH9 mediated by direct repeat elements.

作者信息

Ogawa N, Miyashita K

机构信息

National Institute of Agro-Environmental Sciences, Ibaraki, Japan.

出版信息

Appl Environ Microbiol. 1995 Nov;61(11):3788-95. doi: 10.1128/aem.61.11.3788-3795.1995.

Abstract

Alcaligenes eutrophus NH9 was isolated from soil. This strain can utilize 3-chlorobenzoate (3-CB) as a sole source of carbon and energy. Most of the 3-CB-negative segregants had lost one of the plasmids present in the parent strain. The genes for catabolism of 3-CB were located within a 9.2-kb SacI fragment of this plasmid (pENH91). The genes were found to hybridize with genes for components of the modified ortho cleavage pathway from Pseudomonas putida. In one of the 3-CB-negative segregants, the plasmid had undergone the deletion of a segment with a size of about 12.5 kb that covered the catabolic genes. The deletion event seemed to be the result of reciprocal recombination between two highly homologous sequences with sizes of 2.5 kb that were present as a direct repeat at the two ends of the region that included the catabolic genes. Nucleotide sequence analysis of homologous fragments revealed a structure that resembled an insertion sequence and relatedness to IS21. During repeated subculturing of NH9 on liquid media with 3-CB, the culture was taken over by a derivative strain (designated NH9A) in which the degradative plasmid carried a duplicate copy of the 12.5-kb region that contained the catabolic genes. The duplication of these genes seemed again to have been mediated by recombination between the direct repeat sequences.

摘要

嗜碱产碱杆菌NH9是从土壤中分离得到的。该菌株能够利用3 - 氯苯甲酸(3 - CB)作为唯一的碳源和能源。大多数3 - CB阴性分离株丢失了亲代菌株中存在的一种质粒。3 - CB分解代谢基因位于该质粒(pENH91)的一个9.2 kb的SacI片段内。发现这些基因与恶臭假单胞菌改良邻位裂解途径的组分基因杂交。在其中一个3 - CB阴性分离株中,质粒发生了约12.5 kb片段的缺失,该片段包含分解代谢基因。缺失事件似乎是两个大小为2.5 kb的高度同源序列之间相互重组的结果,这两个序列以正向重复的形式存在于包含分解代谢基因的区域两端。同源片段的核苷酸序列分析揭示了一种类似于插入序列的结构,并且与IS21相关。在含有3 - CB的液体培养基上对NH9进行反复传代培养时,培养物被一个衍生菌株(命名为NH9A)取代,在该衍生菌株中,降解性质粒携带了包含分解代谢基因的12.5 kb区域的重复拷贝。这些基因的重复似乎再次是由正向重复序列之间的重组介导的。

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