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苏云金芽孢杆菌质粒pTX14-3复制功能的精细定位与DNA序列分析

Fine mapping and DNA sequence of replication functions of Bacillus thuringiensis plasmid pTX14-3.

作者信息

Madsen S M, Andrup L, Boe L

机构信息

Department of Microbiology, Technical University of Denmark, Lyngby-Copenhagen.

出版信息

Plasmid. 1993 Sep;30(2):119-30. doi: 10.1006/plas.1993.1039.

Abstract

pTX14-3 is a 7.5-kb cryptic plasmid isolated from a Bacillus thuringiensis subspecies israelensis strain. Like many other small plasmids in gram-positive bacteria, pTX14-3 replicates via a single-stranded DNA intermediate. The nucleotide sequence of the replication region was determined and an open reading frame of 636 base pairs encoding a protein necessary for plasmid replication was identified by deletion analysis. No significant homology was found between this open reading frame and those encoding replication proteins identified on other plasmids isolated from gram-positive bacteria, nor could we find any homology to plus origins from other single-stranded DNA plasmids. Consequently, it seems that the replicon of pTX14-3 belongs to a new family of replicons in the group of single-stranded DNA plasmids. The sequence of the single-strand origin (i.e., the minus origin) responsible for the conversion of single-stranded plasmid DNA to double-stranded plasmid DNA was also determined. A partial homology between the minus origin of pTX14-3 and the Bacillus subtilis plasmid pBAA1 was identified. A previously identified locus that suppresses formation of high molecular weight multimers was also minimized and sequenced.

摘要

pTX14 - 3是从苏云金芽孢杆菌以色列亚种菌株中分离出的一个7.5千碱基对的隐蔽质粒。与革兰氏阳性菌中的许多其他小质粒一样,pTX14 - 3通过单链DNA中间体进行复制。测定了复制区域的核苷酸序列,并通过缺失分析鉴定出一个编码质粒复制所需蛋白质的636个碱基对的开放阅读框。在这个开放阅读框与从革兰氏阳性菌中分离出的其他质粒上鉴定出的编码复制蛋白的开放阅读框之间未发现明显同源性,我们也未发现与其他单链DNA质粒的正链起点有任何同源性。因此,pTX14 - 3的复制子似乎属于单链DNA质粒组中的一个新的复制子家族。还测定了负责单链质粒DNA转化为双链质粒DNA的单链起点(即负链起点)的序列。鉴定出pTX14 - 3的负链起点与枯草芽孢杆菌质粒pBAA1之间存在部分同源性。一个先前鉴定出的抑制高分子量多聚体形成的位点也被最小化并进行了测序。

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