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质粒pSE101在红色糖多孢菌和变铅青链霉菌中进行位点特异性整合的基因及附着位点的表征

Characterization of the genes and attachment sites for site-specific integration of plasmid pSE101 in Saccharopolyspora erythraea and Streptomyces lividans.

作者信息

Brown D P, Idler K B, Backer D M, Donadio S, Katz L

机构信息

Department of Molecular Biology, Abbott Laboratories, Abbott Park, IL 60064.

出版信息

Mol Gen Genet. 1994 Jan;242(2):185-93. doi: 10.1007/BF00391012.

Abstract

The 11.3 kb plasmid pSE101 integrates into the chromosome of Saccharopolyspora erythraea at a specific attB site and into the chromosome of Streptomyces lividans at many sites. Multisite integration in S. lividans was also observed when a 1.9 kb segment of pSE101 containing attP and adjacent plasmid sequence was used to transform a pSE101- S. lividans host. Nucleotide sequencing of this segment revealed the presence of a complete open reading frame (ORF) designated int, encoding a putative polypeptide of 448 amino acids that shows similarities to site-specific recombinases of the integrase family. Sequencing of the 1.3 kb segment upstream of int revealed the presence of three additional ORFs: the one most distal to int encodes a putative 76 amino acid basic polypeptide analogous to the Xis proteins of a number of bacteriophages. Nucleotide sequencing of attP, and the attB, attL and attR sites from Sac. erythraea revealed a 46 bp sequence common to all sites with no duplications of chromosomal sequences in the integrated state. A putative structural gene for a tRNA(Thr) was found to overlap the 46 bp common sequence at attB. Sequencing of four pSE101 integration sites (attB') and corresponding attL' and attR' sites in S. lividans showed that the 46 bp sequence was present at each attR' site, whereas only the first three bases, CTT, were retained at each attL' and attB' site. A feature common to the four attB' sites and to attB is a highly conserved 21 bp segment with inverted repeats flanking the CTT sequence.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

11.3 kb的质粒pSE101在特定的attB位点整合到糖多孢红霉菌的染色体中,并在多个位点整合到变铅青链霉菌的染色体中。当使用含有attP和相邻质粒序列的1.9 kb的pSE101片段转化pSE101-变铅青链霉菌宿主时,也观察到在变铅青链霉菌中的多位点整合。该片段的核苷酸测序揭示了一个完整的开放阅读框(ORF)的存在,该阅读框被命名为int,编码一个推定的448个氨基酸的多肽,该多肽与整合酶家族的位点特异性重组酶具有相似性。int上游1.3 kb片段的测序揭示了另外三个ORF的存在:离int最远的一个编码一个推定的76个氨基酸的碱性多肽,类似于许多噬菌体的Xis蛋白。来自糖多孢红霉菌的attP以及attB, attL和attR位点的核苷酸测序揭示了所有位点共有的46 bp序列,在整合状态下没有染色体序列的重复。发现一个tRNA(Thr)的推定结构基因与attB处的46 bp共有序列重叠。变铅青链霉菌中四个pSE101整合位点(attB')以及相应的attL'和attR'位点的测序表明,每个attR'位点都存在46 bp序列,而每个attL'和attB'位点仅保留前三个碱基CTT。四个attB'位点和attB共有的一个特征是一个高度保守的21 bp片段,CTT序列两侧有反向重复序列。(摘要截短为250字)

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