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用于核糖体结合位点遗传测定的无标记大肠杆菌rrn缺失菌株

Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites.

作者信息

Quan Selwyn, Skovgaard Ole, McLaughlin Robert E, Buurman Ed T, Squires Catherine L

机构信息

Department of Biology, Stanford University, Stanford, California 094305.

Department of Science, Systems and Models, Roskilde University, DK-4000 Roskilde, Denmark.

出版信息

G3 (Bethesda). 2015 Oct 4;5(12):2555-7. doi: 10.1534/g3.115.022301.

Abstract

Single-copy rrn strains facilitate genetic ribosomal studies in Escherichia coli. Consecutive markerless deletion of rrn operons resulted in slower growth upon inactivation of the fourth copy, which was reversed by supplying transfer RNA genes encoded in rrn operons in trans. Removal of the sixth, penultimate rrn copy led to a reduced growth rate due to limited rrn gene dosage. Whole-genome sequencing of variants of single-copy rrn strains revealed duplications of large stretches of genomic DNA. The combination of selective pressure, resulting from the decreased growth rate, and the six identical remaining scar sequences, facilitating homologous recombination events, presumably leads to elevated genomic instability.

摘要

单拷贝rrn菌株有助于在大肠杆菌中进行核糖体遗传学研究。rrn操纵子的连续无标记缺失导致第四个拷贝失活后生长变慢,通过反式提供rrn操纵子中编码的转运RNA基因可使其恢复。去除第六个(倒数第二个)rrn拷贝会因rrn基因剂量有限而导致生长速率降低。单拷贝rrn菌株变体的全基因组测序揭示了大片段基因组DNA的重复。生长速率降低所产生的选择压力与六个相同的剩余疤痕序列相结合,促进了同源重组事件,这可能导致基因组不稳定性升高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a6f/4683628/58e76825058d/2555f1.jpg

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