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噬菌体抗性质粒pTR2030在乳酸乳球菌中形成高分子量多聚体。

The bacteriophage resistance plasmid pTR2030 forms high-molecular-weight multimers in lactococci.

作者信息

Hill C, Miller L A, Klaenhammer T R

机构信息

Department of Food Science, Southeast Dairy Foods Research Center, North Carolina State University, Raleigh 27695-7625.

出版信息

Plasmid. 1991 Mar;25(2):105-12. doi: 10.1016/0147-619x(91)90021-n.

Abstract

Lactococcus lactis ME2 can transfer a 46-kb plasmid, pTR2030, which encodes abortive phage infection (Hsp) and restriction/modification (R/M) activities. pTR2030 can be detected as a monomeric plasmid in transconjugants at low copy number, but not in ME2. pTR2030-specific probes were cloned and used to determine the location of the element in ME2. No homology was observed between these pTR2030-specific probes and the CsCl-purified plasmid content of ME2. However, probes specific for pTR2030 hybridized strongly to a high-molecular-weight moiety, and not to chromosomal DNA, in total DNA isolated by a gentle lysis procedure. The absence of junction fragments indicates that pTR2030 forms high-molecular-weight multimers in lactococci. A phage-sensitive derivative of ME2, L. lactis N1, is cured of pTR2030 and no longer possesses the high-molecular-weight species. When pTR2030 was reintroduced to N1 via conjugation, an ME2-like phage-insensitive phenotype was restored. pTR2030 could remain as a detectable monomeric plasmid in the N1 transconjugants or could revert to the high-molecular-weight structure.

摘要

乳酸乳球菌ME2能够转移一个46 kb的质粒pTR2030,该质粒编码流产噬菌体感染(Hsp)和限制/修饰(R/M)活性。在转接合子中,pTR2030可以以低拷贝数的单体质粒形式被检测到,但在ME2中则不然。克隆了pTR2030特异性探针,并用于确定该元件在ME2中的位置。这些pTR2030特异性探针与ME2经氯化铯纯化的质粒含量之间未观察到同源性。然而,在通过温和裂解程序分离的总DNA中,pTR2030特异性探针与高分子量部分强烈杂交,而不与染色体DNA杂交。连接片段的缺失表明pTR2030在乳球菌中形成高分子量多聚体。ME2的噬菌体敏感衍生物乳酸乳球菌N1不含pTR2030,也不再具有高分子量物质。当通过接合将pTR2030重新引入N1时,恢复了类似ME2的噬菌体不敏感表型。pTR2030可以作为可检测的单体质粒保留在N1转接合子中,也可以恢复为高分子量结构。

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