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长头乳球菌噬菌体c2基因组的测序与分析及结构基因的鉴定

Sequencing and analysis of the prolate-headed lactococcal bacteriophage c2 genome and identification of the structural genes.

作者信息

Lubbers M W, Waterfield N R, Beresford T P, Le Page R W, Jarvis A W

机构信息

Biological Science Section, New Zealand Dairy Research Institute, Palmerston North, New Zealand.

出版信息

Appl Environ Microbiol. 1995 Dec;61(12):4348-56. doi: 10.1128/aem.61.12.4348-4356.1995.

Abstract

The 22,163-bp genome of the lactococcal prolate-headed phage c2 was sequenced. Thirty-nine open reading frames (ORFs), early and late promoters, and a putative transcription terminator were identified. Twenty-two ORFs were in the early gene region, and 17 were in the late gene region. Putative genes for a DNA polymerase, a recombination protein, a sigma factor protein, a transcription regulatory protein, holin proteins, and a terminase were identified. Transcription of the early and late genes proceeded divergently from a noncoding 611-bp region. A 521-bp fragment contained within the 611-bp intergenic region could act as an origin of replication in Lactococcus lactis. Three major structural proteins, with sizes of 175, 90, and 29 kDa, and eight minor proteins, with sizes of 143, 82, 66, 60, 44, 42, 32, and 28 kDa, were identified. Several of these proteins appeared to be posttranslationally modified by proteolytic cleavage. The 175- and 90-kDa proteins were identified as the major phage head proteins, and the 29- and 60-kDa proteins were identified as the major tail protein and (possibly) the tail adsorption protein, respectively. The head proteins appeared to be covalently linked multimers of the same 30-kDa gene product. Phage c2 and prolate-headed lactococcal phage bIL67 (C. Schouler, S. D. Ehrlich, and M.-C. Chopin, Microbiology 140:3061-3069, 1994) shared 80% nucleotide sequence identity. However, several DNA deletions or insertions which corresponded to the loss or acquisition of specific ORFs, respectively, were noted. The identification of direct nucleotide repeats flanking these sequences indicated that recombination may be important in the evolution of these phages.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对乳球菌属长头噬菌体c2的22163碱基对基因组进行了测序。鉴定出39个开放阅读框(ORF)、早期和晚期启动子以及一个假定的转录终止子。22个ORF位于早期基因区域,17个位于晚期基因区域。鉴定出了假定的DNA聚合酶、重组蛋白、σ因子蛋白、转录调节蛋白、穿孔素蛋白和末端酶基因。早期和晚期基因的转录从一个611碱基对的非编码区域向不同方向进行。611碱基对基因间隔区内包含的一个521碱基对片段可作为乳酸乳球菌中的复制起点。鉴定出三种主要结构蛋白,大小分别为175、90和29 kDa,以及八种次要蛋白,大小分别为143、82、66、60、44、42、32和28 kDa。其中几种蛋白似乎经过蛋白水解切割进行了翻译后修饰。175 kDa和90 kDa的蛋白被鉴定为主要的噬菌体头部蛋白,29 kDa和60 kDa的蛋白分别被鉴定为主要的尾部蛋白和(可能的)尾部吸附蛋白。头部蛋白似乎是同一30 kDa基因产物的共价连接多聚体。噬菌体c2与长头乳球菌噬菌体bIL67(C. Schouler、S. D. Ehrlich和M.-C. Chopin,《微生物学》140:3061 - 3069,1994)共享80%的核苷酸序列同一性。然而,注意到了几个分别对应于特定ORF缺失或获得的DNA缺失或插入。这些序列侧翼直接核苷酸重复序列的鉴定表明重组可能在这些噬菌体的进化中起重要作用。(摘要截短至250字)

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Transcription analysis of the prolate-headed lactococcal bacteriophage c2.长头乳球菌噬菌体c2的转录分析
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