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染色体整合后回收的复制缺陷型RP4质粒。

Replication defective RP4 plasmids recovered after chromosomal integration.

作者信息

Grinter N J

出版信息

Plasmid. 1984 Jan;11(1):65-73. doi: 10.1016/0147-619x(84)90008-8.

Abstract

pHH6000 is a composite replicon made by the in vitro ligation of the IncP plasmid RP4 to a fragment of bacteriophage lambda capable of autonomous replication. Derivatives were selected in which it had integrated into the Escherichia coli chromosome by homologous recombination with the resident lambda prophage, and plasmids were subsequently regenerated from the integrated molecules. Although of the same molecular size as pHH6000, all had altered properties: those recovered from the chromosome of cells simultaneously carrying a distinguishable autonomous IncP plasmid showed a 100- to 1000-fold reduction in their ability to become established in a lambda lysogen; those regenerated from cells with no autonomous IncP plasmid were no longer RP4 replicons, now being dependent on replication functions encoded by the lambda DNA they carry and therefore unable to form a plasmid in a lambda lysogen. This second class of plasmids still exhibited normal RP4 incompatibility and stability even though neither property is encoded by the lambda replicator DNA. It was concluded that expression of RP4 incompatibility and partitioning control do not require an intact RP4 replicon. The data also suggest that the presence in the chromosome of a normal RP4 molecule may be deleterious to the host, although the manner in which the integrated molecules were obtained allows other explanations. The composite plasmids replicating from cloned lambda genes should be useful in analysis of the regulated distribution of RP4 molecules at cell division.

摘要

pHH6000是一种复合复制子,它由IncP质粒RP4与能够自主复制的噬菌体λ片段在体外连接而成。通过与宿主λ原噬菌体进行同源重组,筛选出已整合到大肠杆菌染色体中的衍生物,随后从整合分子中再生出质粒。尽管所有衍生物的分子大小与pHH6000相同,但它们的特性均发生了改变:从同时携带可区分的自主IncP质粒的细胞染色体中回收的衍生物,在λ溶原菌中建立的能力降低了100至1000倍;从没有自主IncP质粒的细胞中再生的衍生物不再是RP4复制子,现在依赖于它们所携带的λDNA编码的复制功能,因此无法在λ溶原菌中形成质粒。尽管这第二类质粒的不相容性和稳定性都不是由λ复制子DNA编码的,但它们仍然表现出正常的RP4不相容性和稳定性。得出的结论是,RP4不相容性和分配控制的表达不需要完整的RP4复制子。数据还表明,正常RP4分子存在于染色体中可能对宿主有害,尽管获得整合分子的方式也有其他解释。从克隆的λ基因复制的复合质粒在分析RP4分子在细胞分裂时的调控分布方面应该是有用的。

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