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F质粒oriT处切口的位置。

Location of the nick at oriT of the F plasmid.

作者信息

Thompson T L, Centola M B, Deonier R C

机构信息

Department of Biological Sciences, University of Southern California, Los Angeles 90089-1340.

出版信息

J Mol Biol. 1989 Jun 5;207(3):505-12. doi: 10.1016/0022-2836(89)90460-9.

DOI:10.1016/0022-2836(89)90460-9
PMID:2668533
Abstract

The oriT locus of the Escherichia coli K12 F plasmid contains a site at which one of the DNA strands is cleaved as a prelude to conjugal transmission to recipient bacteria. We have remapped this site biochemically by using oriT-containing plasmids that were purified from bacteria expressing the F transfer (tra) functions. The strand interruption was found on the transferred strand 137 base-pairs clockwise of the center of the BglII site at 66.7 on the F map. This location is consistent with the locations anticipated from studies of delta traF' plasmids, but it differs from previous results by other investigators. The strand interruption produced a 3'-OH, but the nature of the 5' terminus of the strand on the other side of the nick was not determined. Some DNA sequence motifs in the vicinity of the oriT nick site of F resemble the chromosomal site involved in formation of delta traF'purE plasmids.

摘要

大肠杆菌K12 F质粒的oriT位点包含一个DNA链被切割的位点,这是向受体细菌进行接合转移的前奏。我们通过使用从表达F转移(tra)功能的细菌中纯化的含oriT质粒,对该位点进行了生化重定位。发现链中断位于F图谱上66.7处BglII位点中心顺时针137个碱基对的转移链上。该位置与对δtraF'质粒研究预期的位置一致,但与其他研究者先前的结果不同。链中断产生了一个3'-OH,但切口另一侧链的5'末端性质未确定。F的oriT切口位点附近的一些DNA序列基序类似于参与形成δtraF'purE质粒的染色体位点。

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1
Location of the nick at oriT of the F plasmid.F质粒oriT处切口的位置。
J Mol Biol. 1989 Jun 5;207(3):505-12. doi: 10.1016/0022-2836(89)90460-9.
2
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引用本文的文献

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Mobilization of chimeric oriT plasmids by F and R100-1: role of relaxosome formation in defining plasmid specificity.F和R100-1对嵌合oriT质粒的动员:松弛体形成在确定质粒特异性中的作用
J Bacteriol. 2000 Jul;182(14):4022-7. doi: 10.1128/JB.182.14.4022-4027.2000.
2
IncP plasmids are unusually effective in mediating conjugation of Escherichia coli and Saccharomyces cerevisiae: involvement of the tra2 mating system.IncP质粒在介导大肠杆菌和酿酒酵母的接合方面异常有效:tra2交配系统的作用。
J Bacteriol. 1998 Dec;180(24):6538-43. doi: 10.1128/JB.180.24.6538-6543.1998.
3
Localization of the nic site of IncN conjugative plasmid pCU1 through formation of a hybrid oriT.
通过形成杂交oriT对IncN接合质粒pCU1的nic位点进行定位。
J Bacteriol. 1997 Sep;179(18):5768-76. doi: 10.1128/jb.179.18.5768-5776.1997.
4
Specific cleavage of chromosomal and plasmid DNA strands in gram-positive and gram-negative bacteria can be detected with nucleotide resolution.革兰氏阳性菌和革兰氏阴性菌中染色体和质粒DNA链的特异性切割可以通过核苷酸分辨率检测到。
Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7435-40. doi: 10.1073/pnas.94.14.7435.
5
Characterization of the reaction product of the oriT nicking reaction catalyzed by Escherichia coli DNA helicase I.由大肠杆菌DNA解旋酶I催化的oriT切口反应产物的特性分析。
J Bacteriol. 1993 May;175(9):2599-606. doi: 10.1128/jb.175.9.2599-2606.1993.
6
Analysis of the sequence and gene products of the transfer region of the F sex factor.F 性因子转移区域的序列及基因产物分析
Microbiol Rev. 1994 Jun;58(2):162-210. doi: 10.1128/mr.58.2.162-210.1994.
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J Bacteriol. 1995 Aug;177(15):4279-88. doi: 10.1128/jb.177.15.4279-4288.1995.
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J Bacteriol. 1990 Mar;172(3):1385-91. doi: 10.1128/jb.172.3.1385-1391.1990.
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