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鱼腥藻属PCC 7120菌株中不能在有氧条件下以二氮生长的突变体的分离与互补

Isolation and complementation of mutants of Anabaena sp. strain PCC 7120 unable to grow aerobically on dinitrogen.

作者信息

Wolk C P, Cai Y, Cardemil L, Flores E, Hohn B, Murry M, Schmetterer G, Schrautemeier B, Wilson R

机构信息

MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing 48824.

出版信息

J Bacteriol. 1988 Mar;170(3):1239-44. doi: 10.1128/jb.170.3.1239-1244.1988.

Abstract

Mutants of Anabaena sp. strain PCC 7120 unable to grow aerobically on dinitrogen were isolated by mutagenesis with UV irradiation, followed by a period of incubation in yellow light and then by penicillin enrichment. A cosmid vector, pRL25C, containing replicons functional in Escherichia coli and in Anabaena species was constructed. DNA from wild-type Anabaena sp. strain PCC 7120 was partially digested with Sau3AI, and size-fractionated fragments about 40 kilobases (kb) in length were ligated into the phosphatase-treated unique BamHI site of pRL25C. A library of 1,054 cosmid clones was generated in E. coli DH1 bearing helper plasmid pDS4101. A derivative of conjugative plasmid RP-4 was transferred to this library by conjugation, and the library was replicated to lawns of mutant Anabaena strains with defects in the polysaccharide layer of the envelopes of the heterocysts. Mutant EF116 was complemented by five cosmids, three of which were subjected to detailed restriction mapping; a 2.8-kb fragment of DNA derived from one of the cosmids was found to complement EF116. Mutant EF113 was complemented by a single cosmid, which was also restriction mapped, and was shown to be complemented by a 4.8-kb fragment of DNA derived from this cosmid.

摘要

通过紫外线诱变,随后在黄光下培养一段时间,再经青霉素富集,分离得到了鱼腥藻PCC 7120菌株中无法在有氧条件下以二氮生长的突变体。构建了一种黏粒载体pRL25C,其含有在大肠杆菌和鱼腥藻属中具有功能的复制子。用Sau3AI对野生型鱼腥藻PCC 7120菌株的DNA进行部分消化,将长度约40千碱基(kb)的大小分级片段连接到经碱性磷酸酶处理的pRL25C的唯一BamHI位点。在携带辅助质粒pDS4101的大肠杆菌DH1中产生了一个包含1054个黏粒克隆的文库。通过接合将接合性质粒RP - 4的一个衍生物转移到该文库中,并将该文库复制到异形胞包膜多糖层有缺陷的突变鱼腥藻菌株的菌苔上。突变体EF116由五个黏粒互补,其中三个进行了详细的限制性图谱分析;发现来自其中一个黏粒的2.8 kb DNA片段可互补EF116。突变体EF113由一个单一黏粒互补,该黏粒也进行了限制性图谱分析,并显示由来自该黏粒的4.8 kb DNA片段互补。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4033/210898/680881fd571d/jbacter00181-0225-a.jpg

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