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枯草芽孢杆菌中源自pSM19035的质粒pBT233稳定系统的分析

Analysis of the stabilization system of pSM19035-derived plasmid pBT233 in Bacillus subtilis.

作者信息

Cegłowski P, Boitsov A, Chai S, Alonso J C

机构信息

Max-Planck-Institut für Molekulare Genetik, Berlin, Germany.

出版信息

Gene. 1993 Dec 22;136(1-2):1-12. doi: 10.1016/0378-1119(93)90441-5.

Abstract

The low-copy-number, 9.0-kb pSM19035-derived plasmid pBT233, is stably inherited in Bacillus subtilis. The complete nucleotide (nt) sequence of pBT233 has been determined. Analysis of the nt sequence revealed nine major open reading frames (orfs). The repS, erm1 and erm2 genes have been assigned to three of these orfs, and given the gene order, repS-orf alpha-orf beta-orf gamma-orf delta-orf epsilon-orf zeta-erm2-erm1. The organization of genes of the repS-orf gamma region resembles the organization of genes in the repE-orfI region of pAM beta 1. Messenger RNA species of molecular weights corresponding to repS, orf alpha + orf beta, orf gamma, orf delta and orf epsilon + orf zeta were detected by Northern blotting. Proteins of 23.8, 81.3, 34.4, 10.7 and 32.4 kDa correspond to Orfs beta, gamma, delta, epsilon and zeta, respectively. Bands of radioactive proteins of 25, 81, 34, 10 and 32 kDa were detected using the T7 promoter-expression system. The orf beta and orf gamma encode proteins that share homology to site-specific recombinases and type-I topoisomerases, respectively. The orfs, delta, epsilon and zeta, encode proteins with unknown activity. Deletion of a 1.5-kb segment (nt 2999-4552) with coding capacity for orf beta, orf gamma and orf delta does not seem to affect plasmid maintenance. Removal of a 3.0-kb fragment (nt 4598-7689) with coding capacity for orf epsilon and orf zeta reduced plasmid segregational stability, but deletion of a 5.2-kb DNA segment (nt 2546-7826) abolished it.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

低拷贝数、源自9.0 kb的pSM19035的质粒pBT233在枯草芽孢杆菌中稳定遗传。已确定pBT233的完整核苷酸(nt)序列。对nt序列的分析揭示了9个主要的开放阅读框(orfs)。repS、erm1和erm2基因已被指定到其中3个orfs上,基因顺序为repS-orfα-orfβ-orfγ-orfδ-orfε-orfζ-erm2-erm1。repS-orfγ区域的基因组织类似于pAMβ1的repE-orfI区域的基因组织。通过Northern印迹检测到分子量与repS、orfα + orfβ、orfγ、orfδ和orfε + orfζ相对应的信使RNA种类。23.8、81.3、34.4、10.7和32.4 kDa的蛋白质分别对应于Orfsβ、γ、δ、ε和ζ。使用T7启动子表达系统检测到25、81、34、10和32 kDa的放射性蛋白质条带。orfβ和orfγ分别编码与位点特异性重组酶和I型拓扑异构酶具有同源性的蛋白质。orfsδ、ε和ζ编码具有未知活性的蛋白质。缺失具有orfβ、orfγ和orfδ编码能力的1.5 kb片段(nt 2999 - 4552)似乎不影响质粒的维持。去除具有orfε和orfζ编码能力的3.0 kb片段(nt 4598 - 7689)降低了质粒的分离稳定性,但缺失5.2 kb的DNA片段(nt 2546 - 7826)则消除了这种稳定性。(摘要截短于250字)

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