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携带染色体trpE-ilvA和purB-tre区域两个非串联重复序列的枯草芽孢杆菌菌株。

Bacillus subtilis strains carrying two non-tandem duplications of the trpE-ilvA and the purB-tre regions of the chromosome.

作者信息

Schneider A M, Anagnostopoulos C

出版信息

J Gen Microbiol. 1983 Mar;129(3):687-701. doi: 10.1099/00221287-129-3-687.

Abstract

Bacillus subtilis strains possessing the trpE30 marker (splitting of the trpE locus and a non-tandem duplication of chromosome segment Ib: purB-tre) when transformed or transduced to tryptophan independence mainly give rise to haploid cells with the genetic structure of strain 168. However, among the Trp+ transformants or transductants about 10% are merodiploid carrying a non-tandem duplication of segment C (trpE-ilvA) while maintaining that of segment Ib. Linkage and segregation studies made it possible to determine their genetic structure, which can be represented by three different maps. In map a the copies of Ib are inverted repeats and one of them is flanked by two direct repeats of segment C; in map b two Ib-C segments are inverted repeats and in map c the copies of C are inverted repeats with one of them flanked by direct repeats of Ib. It is proposed that transition from map a to map b and then to map c, and vice versa, may occur by recombination between inverted repeats of either Ib or C. The merodiploids are unstable, recombination between direct repeats leading to haploid cells of 168-type structure. The models proposed for merodiploid formation call for fusion of two recipient chromosomes mediated by the donor segment and recombination between copies of a DNA sequence of the two chromosomes located in different regions. In the case of PBS-1 mediated transduction the greater length of the donor DNA segment makes it possible to obtain the merodiploids with a single recipient chromosome and this needs only a slight modification of the models. No trpE30+ merodiploids are found in transformation when the recipient carries a deletion of the SP beta prophage, or in transduction when both donor and recipient possess this deletion. These results indicate that the homologous sequences involved may be part of the SP beta prophage or that a sequence of bacterial DNA has a good homology with it.

摘要

具有trpE30标记(trpE基因座分裂以及染色体片段Ib:purB - tre的非串联重复)的枯草芽孢杆菌菌株在转化或转导至色氨酸自主时,主要产生具有168菌株遗传结构的单倍体细胞。然而,在Trp +转化体或转导体中,约10%是部分二倍体,携带片段C(trpE - ilvA)的非串联重复,同时保留片段Ib的重复。连锁和分离研究使得确定它们的遗传结构成为可能,其可以由三种不同的图谱表示。在图谱a中,Ib的拷贝是反向重复序列,其中一个侧翼是片段C的两个正向重复序列;在图谱b中,两个Ib - C片段是反向重复序列,在图谱c中,C的拷贝是反向重复序列,其中一个侧翼是Ib的正向重复序列。有人提出,从图谱a到图谱b再到图谱c的转变,反之亦然,可能通过Ib或C的反向重复序列之间的重组发生。部分二倍体不稳定,正向重复序列之间的重组导致168型结构的单倍体细胞。为部分二倍体形成提出的模型要求由供体片段介导的两个受体染色体融合以及位于不同区域的两条染色体的DNA序列拷贝之间的重组。在PBS - 1介导的转导情况下,供体DNA片段的较长长度使得有可能获得具有单个受体染色体的部分二倍体,这只需要对模型进行轻微修改。当受体携带SPβ原噬菌体缺失时,在转化中未发现trpE30 +部分二倍体,或者当供体和受体都具有该缺失时,在转导中也未发现。这些结果表明,所涉及的同源序列可能是SPβ原噬菌体的一部分,或者细菌DNA的一个序列与其具有良好的同源性。

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