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来自集胞藻属PCC 6803菌株的一个小质粒pCA2.4编码一种复制蛋白,并通过滚环机制进行复制。

A small plasmid, pCA2.4, from the cyanobacterium Synechocystis sp. strain PCC 6803 encodes a rep protein and replicates by a rolling circle mechanism.

作者信息

Yang X, McFadden B A

机构信息

Department of Biochemistry and Biophysics, Washington State University, Pullman 99164-4660.

出版信息

J Bacteriol. 1993 Jul;175(13):3981-91. doi: 10.1128/jb.175.13.3981-3991.1993.

DOI:10.1128/jb.175.13.3981-3991.1993
PMID:8320214
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC204826/
Abstract

Different cryptic plasmids are widely distributed in many strains of cyanobacteria. A small cryptic plasmid, pCA2.4, from Synechocystis strain PCC 6803 was completely sequenced, and its replication mode was determined. pCA2.4 contained 2,378 bp and encoded a replication (Rep) protein, designated RepA. An analysis of the deduced amino acid sequence revealed that RepA of pCA2.4 has significant homology with Rep proteins of pKYM from Shigella sonnei, a pUB110 plasmid family from gram-positive bacteria, and with a protein corresponding to an open reading frame in a Nostoc plasmid and open reading frame C of Plectonema plasmid pRF1. pKYM and pUB110 family plasmids replicate by a rolling circle mechanism in which a Rep protein nicks the origin of replication to allow the generation of a single-stranded plasmid as a replication intermediate. RepA encoded by pC2.4 was expressed in Escherichia coli cells harboring a vector, pCRP336, containing the entire repA gene. The observed molecular weight of RepA was consistent with the value of 39,200 calculated from its deduced amino acid sequence, as was the N-terminal sequence analysis done through the 12th residue. Single-stranded plasmid DNA of pCA2.4 that was specifically degraded by S1 nuclease was detected in Synechocystis cells by Southern hybridization. These observations suggest that pCA2.4 replicates by a rolling circle mechanism in Synechocystis cells.

摘要

不同的隐蔽质粒广泛分布于许多蓝藻菌株中。对来自集胞藻PCC 6803菌株的一个小型隐蔽质粒pCA2.4进行了全序列测定,并确定了其复制模式。pCA2.4含有2378个碱基对,编码一种复制(Rep)蛋白,命名为RepA。对推导的氨基酸序列分析表明,pCA2.4的RepA与宋内志贺菌的pKYM、革兰氏阳性菌的pUB110质粒家族的Rep蛋白以及与念珠藻质粒中的一个开放阅读框和席藻质粒pRF1的开放阅读框C对应的一种蛋白质具有显著同源性。pKYM和pUB110家族质粒通过滚环机制复制,其中Rep蛋白切割复制起点以产生单链质粒作为复制中间体。由pC2.4编码的RepA在携带含有整个repA基因的载体pCRP336的大肠杆菌细胞中表达。观察到的RepA分子量与根据其推导的氨基酸序列计算出的39200的值一致,通过第12个残基进行的N端序列分析也是如此。通过Southern杂交在集胞藻细胞中检测到被S1核酸酶特异性降解的pCA2.4单链质粒DNA。这些观察结果表明,pCA2.4在集胞藻细胞中通过滚环机制复制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e1e/204826/6e67d43a6091/jbacter00055-0082-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e1e/204826/228a6a2d8d16/jbacter00055-0082-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e1e/204826/6e67d43a6091/jbacter00055-0082-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e1e/204826/228a6a2d8d16/jbacter00055-0082-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e1e/204826/6e67d43a6091/jbacter00055-0082-b.jpg

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