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新型窄宿主范围乳球菌质粒pCI305最小复制子的分子组织

Molecular organization of the minimal replicon of novel, narrow-host-range, lactococcal plasmid pCI305.

作者信息

Hayes F, Vos P, Fitzgerald G F, de Vos W M, Daly C

机构信息

Department of Food Microbiology, University College, Cork, Ireland.

出版信息

Plasmid. 1991 Jan;25(1):16-26. doi: 10.1016/0147-619x(91)90003-f.

Abstract

Plasmid pCI305 is an 8.7-kb, narrow-host-range, cryptic plasmid originating from Lactococcus lactis subsp. lactis UC317. The nucleotide sequence of the pCI305 replication region was determined. A single open reading frame of 1158 bp was identified in the trans-active domain repB. The size of the predicted repB protein (46 kDa) is in close agreement with the size of the repB product visualized in vivo in Escherichia coli when repB was placed under control of the inducible phi T7 RNA polymerase promoter. In vivo substitution of the native repB promoter sequence with a Tn5-derived promoter sequence was demonstrated. repA, a 344-bp cis-acting region which is the probable pCI305 replication origin region, was noncoding, was AT-rich, and possessed a unique set of inverted and direct repeat sequences. No significant homology between repA or repB and other gram-positive replication regions was evident. Combined with the absence of a detectable single-stranded DNA intermediate during replication, these results indicate that the pCI305 replication region differs markedly from most gram-positive replicons examined to date. The presence on other lactococcal plasmids of replication regions related to that of pCI305 was demonstrated.

摘要

质粒pCI305是一种8.7千碱基对的窄宿主范围隐蔽质粒,源自乳酸乳球菌乳酸亚种UC317。测定了pCI305复制区域的核苷酸序列。在反式作用结构域repB中鉴定出一个1158碱基对的单一开放阅读框。预测的repB蛋白大小(46千道尔顿)与当repB置于可诱导的φT7 RNA聚合酶启动子控制下时在大肠杆菌体内观察到的repB产物大小非常一致。证明了用源自Tn5的启动子序列在体内替代天然repB启动子序列。repA是一个344碱基对的顺式作用区域,可能是pCI305的复制起始区域,它是非编码的,富含AT,并拥有一组独特的反向和正向重复序列。repA或repB与其他革兰氏阳性复制区域之间没有明显的同源性。结合复制过程中未检测到单链DNA中间体,这些结果表明pCI305复制区域与迄今为止检测的大多数革兰氏阳性复制子明显不同。证明了其他乳球菌质粒上存在与pCI305复制区域相关的复制区域。

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