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枝动胶菌I-16-M胞外多糖生物合成基因的分离及该区域内不稳定性的证据。

Isolation of Zoogloea ramigera I-16-M exopolysaccharide biosynthetic genes and evidence for instability within this region.

作者信息

Easson D D, Sinskey A J, Peoples O P

机构信息

Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

J Bacteriol. 1987 Oct;169(10):4518-24. doi: 10.1128/jb.169.10.4518-4524.1987.

Abstract

The genetics of the biosynthesis of an exocellular polysaccharide (EPS) from Zoogloea ramigera I-16-M is being investigated. Tn5 insertion mutants deficient in EPS production were isolated by screening for the absence of fluorescence on plates containing the dye Cellufluor (Polysciences Chemicals). Complementation of these mutations was achieved with a Z. ramigera I-16-M gene library constructed in a broad-host-range cosmid vector and introduced into the I-16-M mutants by conjugation. Four recombinant plasmids able to restore EPS production to all of these mutants were found to contain at least 14 kilobases of common insert DNA. Subcloning of the common region and restriction mapping the locations of Tn5 insertions have identified two complementation groups contained within a chromosomal segment of DNA that is between 4.6 and 6.5 kilobases in size. We have clearly demonstrated genetic instability in this region which leads to spontaneous deletions and possibly rearrangements resulting in the loss of EPS production.

摘要

正在研究来自生枝动胶菌I-16-M的一种胞外多糖(EPS)生物合成的遗传学。通过在含有染料Cellufluor(Polysciences Chemicals)的平板上筛选无荧光的情况,分离出了EPS产生缺陷的Tn5插入突变体。用构建在广宿主范围黏粒载体中的生枝动胶菌I-16-M基因文库对这些突变进行互补,并通过接合将其导入I-16-M突变体中。发现四个能够将EPS产生恢复到所有这些突变体的重组质粒含有至少14千碱基的共同插入DNA。对共同区域进行亚克隆并对Tn5插入位置进行限制酶切图谱分析,已确定在一个大小为4.6至6.5千碱基的染色体DNA片段中包含两个互补组。我们已经清楚地证明了该区域的遗传不稳定性,这会导致自发缺失并可能发生重排,从而导致EPS产生的丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5563/213816/421b1ae81410/jbacter00200-0114-a.jpg

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