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首页> 外文期刊>Journal of bacteriology >The Bacteroides mobilizable insertion element, NBU1, integrates into the 3' end of a Leu-tRNA gene and has an integrase that is a member of the lambda integrase family.
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The Bacteroides mobilizable insertion element, NBU1, integrates into the 3' end of a Leu-tRNA gene and has an integrase that is a member of the lambda integrase family.

机译:拟杆菌的可动插入元件NBU1整合到Leu-tRNA基因的3'端,并具有一个整合酶,该整合酶是lambda整合酶家族的成员。

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摘要

NBU1 is a 10.3-kbp integrated Bacteroides element that can be induced to excise from the chromosome and can be mobilized to a recipient by trans-acting functions provided by certain Bacteroides conjugative transposons. The NBU1 transfer intermediate is a covalently closed circle, which is presumed to be the form that integrates into the recipient genome. We report here that a 2.4-kbp segment of NBU1 was all that was required for site-specific integration into the chromosome of Bacteroides thetaiotaomicron 5482. This 2.4-kbp region included the joined ends of the NBU1 circular form (attN1) and a single open reading frame, intN1, which encoded the integrase. Previously, we had found that NBU1 integrates preferentially into a single site in B. thetaiotaomicron 5482. We have now shown that the NBU1 target site is located at the 3' end of a Leu-tRNA gene. The NBU1 integrase gene, intN1, was sequenced. The predicted protein had little overall amino acid sequence similarity to any proteins in the databases but had limited carboxy-terminal similarity to the integrases of lambdoid phages and to the integrases of the gram-positive conjugative transposons Tn916 and Tn1545. We also report that the intN1 gene is expressed constitutively.
机译:NBU1是一个整合了拟南芥的10.3kbp元件,可以被诱导从染色体上切除,并可以通过某些拟南芥共轭转座子所提供的反式作用而动员到受体上。 NBU1转移中间体是一个共价闭合的环,推测是整合到受体基因组中的形式。我们在这里报告,NBU1的2.4 kbp片段是位点特异性整合入拟杆菌Thetaiotaomicron 5482染色体的全部所需。该2.4 kbp区域包括NBU1圆形形式(attN1)的连接末端和一个开放的末端阅读框,intN1,对整合酶进行编码。以前,我们发现NBU1优先整合到B. thetaiotaomicron 5482中的单个位点中。现在我们已经显示NBU1靶位点位于Leu-tRNA基因的3'末端。对NBU1整合酶基因intN1进行了测序。预测的蛋白质与数据库中的任何蛋白质的氨基酸序列相似性均很小,但与lambdoid噬菌体的整合以及革兰氏阳性共轭转座子Tn916和Tn1545的整合具有有限的羧基末端相似性。我们还报告intN1基因组成性表达。

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