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巴西固氮螺菌基因座的分离与鉴定,这些基因座可校正苜蓿根瘤菌的exoB和exoC突变

Isolation and characterization of Azospirillum brasilense loci that correct Rhizobium meliloti exoB and exoC mutations.

作者信息

Michiels K W, Vanderleyden J, Van Gool A P, Signer E R

机构信息

F. A. Janssens Memorial Laboratory for Genetics, Catholic University of Leuven, Heverlee, Belgium.

出版信息

J Bacteriol. 1988 Nov;170(11):5401-4. doi: 10.1128/jb.170.11.5401-5404.1988.

Abstract

The occurrence in Azospirillum brasilense of genes that code for exopolysaccharide (EPS) synthesis was investigated through complementation studies of Rhizobium meliloti Exo- mutants. These mutants are deficient in the synthesis of the major acidic EPS of Rhizobium species and form empty, non-nitrogen-fixing root nodules on alfalfa (J. A. Leigh, E. R. Signer, and G. C. Walker, Proc. Natl. Acad. Sci. USA 82:6231-6235, 1985). We demonstrated that the exoC mutation of R. meliloti could be corrected for EPS production by several cosmid clones of a clone bank of A. brasilense ATCC 29145. However, the EPS produced differed in structure from the wild-type R. meliloti EPS, and the symbiotic deficiency of the exoC mutation was not reversed by any of these cosmid clones. The exoB mutation could be corrected not only for EPS production but also for the ability to form nitrogen-fixing nodules on alfalfa by one particular cosmid clone of A. brasilense. Tn5 insertions in the cloned DNA were isolated and used to construct Azospirillum mutants with mutations in the corresponding loci by marker exchange. It was found that these mutants failed to produce the wild-type high-molecular-weight EPS, but instead produced EPSs of lower molecular weight.

摘要

通过对苜蓿根瘤菌(Rhizobium meliloti)Exo - 突变体的互补研究,调查了巴西固氮螺菌(Azospirillum brasilense)中编码胞外多糖(EPS)合成的基因的存在情况。这些突变体在根瘤菌属主要酸性EPS的合成方面存在缺陷,并且在苜蓿上形成空的、不固氮的根瘤(J. A. Leigh、E. R. Signer和G. C. Walker,《美国国家科学院院刊》82:6231 - 6235,1985年)。我们证明,苜蓿根瘤菌的exoC突变可以通过巴西固氮螺菌ATCC 29145克隆文库的几个黏粒克隆来校正EPS的产生。然而,产生的EPS在结构上与野生型苜蓿根瘤菌EPS不同,并且这些黏粒克隆都没有逆转exoC突变的共生缺陷。exoB突变不仅可以通过巴西固氮螺菌的一个特定黏粒克隆校正EPS的产生,还可以校正其在苜蓿上形成固氮根瘤的能力。分离克隆DNA中的Tn5插入片段,并通过标记交换构建相应位点发生突变的固氮螺菌突变体。发现这些突变体不能产生野生型高分子量EPS,而是产生较低分子量的EPS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7852/211624/3c36aeaf49d3/jbacter00189-0410-a.jpg

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