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信息素诱导表面蛋白Asc10在粪肠球菌质粒pCF10的交配聚集体形成和接合转移中的作用

Role of the pheromone-inducible surface protein Asc10 in mating aggregate formation and conjugal transfer of the Enterococcus faecalis plasmid pCF10.

作者信息

Olmsted S B, Kao S M, van Putte L J, Gallo J C, Dunny G M

机构信息

Institute for Advanced Studies in Biological Process Technology, University of Minnesota, St. Paul 55108.

出版信息

J Bacteriol. 1991 Dec;173(23):7665-72. doi: 10.1128/jb.173.23.7665-7672.1991.

Abstract

The high transfer frequency of pheromone-inducible conjugative plasmids of Enterococcus faecalis in liquid culture is due in part to the formation of mating aggregates. These aggregates result from the interaction of two surface components, aggregation substance (AS), which is plasmid encoded, and the chromosomally encoded binding substance (BS). In the accompanying paper (S.-M. Kao, S. B. Olmsted, A. S. Viksnins, J.C. Gallo, G. M. Dunny, J. Bacteriol, 173:7650-7664, 1991), the sequence of the prgB gene encoding the AS molecule (Asc10) produced by pheromone-induced cells carrying plasmid pCF10 is presented. Here we report the results of genetic and immunological experiments which define the role of Asc10 in aggregation and plasmid transfer. These data indicate expression of AS on the surface of an E. faecalis cell and its binding to BS expressed on a second cell are required for the formation of a mating pair and the efficient transfer of pCF10 in liquid matings. However, the orientation of the receptors was not critical for transfer; ie., AS expressed on recipient cells could facilitate plasmid transfer via binding to BS on the donor. Our results suggest that additional (as yet unidentified) products are involved in forming the channel that ultimately serves to transfer the DNA, with AS-BS binding serving primarily to generate the initial attachment between cells. The putative prgC gene product, identified by DNA sequencing (data presented in the accompanying paper), could be involved in transfer events occurring subsequent to aggregation.

摘要

粪肠球菌信息素诱导的接合质粒在液体培养中的高转移频率部分归因于交配聚集体的形成。这些聚集体是由两种表面成分相互作用产生的,一种是质粒编码的聚集物质(AS),另一种是染色体编码的结合物质(BS)。在随附的论文(S.-M. 高、S. B. 奥尔姆斯特德、A. S. 维克尼斯、J.C. 加洛、G. M. 邓尼,《细菌学杂志》,173:7650 - 7664,1991)中,给出了携带质粒pCF10的信息素诱导细胞产生的编码AS分子(Asc10)的prgB基因序列。在此,我们报告了遗传和免疫学实验的结果,这些实验确定了Asc10在聚集和质粒转移中的作用。这些数据表明,粪肠球菌细胞表面AS的表达及其与另一个细胞上表达的BS的结合是形成交配对以及在液体交配中高效转移pCF10所必需的。然而,受体的方向对转移并不关键;也就是说,受体细胞上表达的AS可以通过与供体细胞上的BS结合来促进质粒转移。我们的结果表明,在形成最终用于转移DNA的通道过程中还涉及其他(尚未鉴定的)产物,而AS - BS结合主要是为了在细胞间产生初始附着。通过DNA测序鉴定的假定prgC基因产物(随附论文中给出的数据)可能参与聚集后发生的转移事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6622/212535/209f4b4bb771/jbacter01041-0272-a.jpg

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