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通过缺失分析对大肠杆菌中的鞭毛基因进行定位

Positioning flagellar genes in Escherichia coli by deletion analysis.

作者信息

Silverman M, Simon M

出版信息

J Bacteriol. 1974 Jan;117(1):73-9. doi: 10.1128/jb.117.1.73-79.1974.

Abstract

Two methods were devised to select a series of overlapping deletion mutations carried on episomal elements in Escherichia coli. The deletions were then used in an analysis of (i) the relative position on the genome of previously described mutant loci in the flagellar genes, (ii) the relative position of a newly defined cistron, flaN, and (iii) the orientation and direction of transcription of genes previously assigned to multicistronic transcriptional units. As a result of this analysis and previous work, we report the following arrangement of the flagellar genes in the his-aroD region of the E. coli genetic map: his-flaR-flaQ-flaP-flaA-flaE-flaO-flaC-flaB-flaN-hag-flaD-uvrC-flaI-mot- flaG-flaH. The genes flaA, P, Q, and R, flaB, C, O and E, and flaG and H are co-transcribed in that order.

摘要

设计了两种方法来选择一系列携带在大肠杆菌附加体元件上的重叠缺失突变。然后将这些缺失用于分析:(i) 鞭毛基因中先前描述的突变位点在基因组上的相对位置;(ii) 新定义的顺反子flaN的相对位置;(iii) 先前分配给多顺反子转录单位的基因的转录方向和取向。作为该分析和先前工作的结果,我们报道了大肠杆菌遗传图谱中his-aroD区域鞭毛基因的以下排列:his-flaR-flaQ-flaP-flaA-flaE-flaO-flaC-flaB-flaN-hag-flaD-uvrC-flaI-mot-flaG-flaH。基因flaA、P、Q和R、flaB、C、O和E以及flaG和H按该顺序共转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aac/246526/affe8268b929/jbacter00343-0085-a.jpg

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