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大肠杆菌B菌株REL606和BL21(DE3)的基因组序列。

Genome sequences of Escherichia coli B strains REL606 and BL21(DE3).

作者信息

Jeong Haeyoung, Barbe Valérie, Lee Choong Hoon, Vallenet David, Yu Dong Su, Choi Sang-Haeng, Couloux Arnaud, Lee Seung-Won, Yoon Sung Ho, Cattolico Laurence, Hur Cheol-Goo, Park Hong-Seog, Ségurens Béatrice, Kim Sun Chang, Oh Tae Kwang, Lenski Richard E, Studier F William, Daegelen Patrick, Kim Jihyun F

机构信息

Korea Research Institute of Bioscience and Biotechnology (KRIBB), 111 Gwahangno, Yuseong, Daejeon 305-806, Korea.

出版信息

J Mol Biol. 2009 Dec 11;394(4):644-52. doi: 10.1016/j.jmb.2009.09.052. Epub 2009 Sep 26.

Abstract

Escherichia coli K-12 and B have been the subjects of classical experiments from which much of our understanding of molecular genetics has emerged. We present here complete genome sequences of two E. coli B strains, REL606, used in a long-term evolution experiment, and BL21(DE3), widely used to express recombinant proteins. The two genomes differ in length by 72,304 bp and have 426 single base pair differences, a seemingly large difference for laboratory strains having a common ancestor within the last 67 years. Transpositions by IS1 and IS150 have occurred in both lineages. Integration of the DE3 prophage in BL21(DE3) apparently displaced a defective prophage in the lambda attachment site of B. As might have been anticipated from the many genetic and biochemical experiments comparing B and K-12 over the years, the B genomes are similar in size and organization to the genome of E. coli K-12 MG1655 and have >99% sequence identity over approximately 92% of their genomes. E. coli B and K-12 differ considerably in distribution of IS elements and in location and composition of larger mobile elements. An unexpected difference is the absence of a large cluster of flagella genes in B, due to a 41 kbp IS1-mediated deletion. Gene clusters that specify the LPS core, O antigen, and restriction enzymes differ substantially, presumably because of horizontal transfer. Comparative analysis of 32 independently isolated E. coli and Shigella genomes, both commensals and pathogenic strains, identifies a minimal set of genes in common plus many strain-specific genes that constitute a large E. coli pan-genome.

摘要

大肠杆菌K-12和B一直是经典实验的研究对象,我们对分子遗传学的许多理解都源于这些实验。我们在此展示了两株大肠杆菌B菌株的完整基因组序列,其中REL606用于一项长期进化实验,而BL21(DE3)广泛用于表达重组蛋白。这两个基因组长度相差72,304 bp,有426个单碱基对差异,对于在过去67年内有共同祖先的实验室菌株来说,这一差异似乎很大。在两个谱系中均发生了IS1和IS150的转座。BL21(DE3)中DE3原噬菌体的整合显然取代了B菌株λ附着位点处的一个缺陷原噬菌体。正如多年来对B和K-12进行的众多遗传和生化实验所预期的那样,B菌株的基因组在大小和组织上与大肠杆菌K-12 MG1655的基因组相似,并且在其约92%的基因组上具有>99%的序列同一性。大肠杆菌B和K-12在IS元件的分布以及较大移动元件的位置和组成方面存在很大差异。一个意外的差异是B菌株中由于一个41 kbp的IS1介导的缺失而没有一大簇鞭毛基因。指定LPS核心、O抗原和限制酶的基因簇有很大差异,可能是由于水平转移。对32个独立分离的大肠杆菌和志贺氏菌基因组(包括共生菌和致病菌株)的比较分析确定了一组最小的共同基因以及许多菌株特异性基因,这些基因构成了一个庞大的大肠杆菌泛基因组。

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