首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Nucleotide sequence determination and genetic analysis of the Bacteroides plasmid, pBI143.
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Nucleotide sequence determination and genetic analysis of the Bacteroides plasmid, pBI143.

机译:拟杆菌(Bacteroides)质粒pBI143的核苷酸序列测定和遗传分析。

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The nucleotide sequence and genetic organization of the Bacteroides plasmid pBI143 were determined. The plasmid was 2747 base pairs (bp) and had a G+C content of 41% (GenBank Accession No. U30316). There were two open reading frames greater than 50 codons and these were designated mobA and repA. A 56-bp inverted repeat divided pBI143 into modules with repA and mobA in separate regions. There was a marked difference in the G+C content and codon usage for the two regions; repA had 33% G+C and mobA was 44% G+C. MobA had homology to other Bacteroides mobilization proteins and RepA shared homology to a replication protein from Zymomonas mobilis plasmid pZM2. These two putative replication proteins formed a subgroup of the rolling-circle replication.proteins belonging to the pSN2 family of gram-positive plasmids. Consistent with this finding, single-stranded pBI143 DNA was detected in plasmid containing Bacteroides fragilis cultures. Availability of the pBI143 sequence allowed the elucidation of the completenucleotide sequence for pFD288 an 8.9-kb Bacteroides shuttle vector (GenBank Accession No. U30830).
机译:确定了拟杆菌质粒pBI143的核苷酸序列和遗传组织。该质粒为2747个碱基对(bp),且G + C含量为41%(GenBank登录号U30316)。有两个大于50个密码子的开放阅读框,分别称为mobA和repA。一个56 bp的反向重复序列将pBI143分为模块,其中repA和mobA在单独的区域中。这两个区域的G + C含量和密码子使用率存在明显差异。 repA的G + C为33%,mobA的G + C为44%。 MobA与其他拟杆菌动员蛋白具有同源性,RepA与运动发酵单胞菌质粒pZM2的复制蛋白具有同源性。这两个推定的复制蛋白形成了滚环复制的一个亚组。该蛋白属于革兰氏阳性质粒的pSN2家族。与该发现一致的是,在含有脆弱拟杆菌的质粒培养物中检测到单链pBI143 DNA。 pBI143序列的可用性允许阐明pFD288和8.9kb的拟杆菌穿梭载体的完整核苷酸序列(GenBank登录号U30830)。

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