Literature DB >> 25725322

Comparative genome analysis of a thermotolerant Escherichia coli obtained by Genome Replication Engineering Assisted Continuous Evolution (GREACE) and its parent strain provides new understanding of microbial heat tolerance.

Guodong Luan1, Guanhui Bao1, Zhao Lin1, Yang Li2, Zugen Chen3, Yin Li4, Zhen Cai5.   

Abstract

Heat tolerance of microbes is of great importance for efficient biorefinery and bioconversion. However, engineering and understanding of microbial heat tolerance are difficult and insufficient because it is a complex physiological trait which probably correlates with all gene functions, genetic regulations, and cellular metabolisms and activities. In this work, a novel strain engineering approach named Genome Replication Engineering Assisted Continuous Evolution (GREACE) was employed to improve the heat tolerance of Escherichia coli. When the E. coli strain carrying a mutator was cultivated under gradually increasing temperature, genome-wide mutations were continuously generated during genome replication and the mutated strains with improved thermotolerance were autonomously selected. A thermotolerant strain HR50 capable of growing at 50°C on LB agar plate was obtained within two months, demonstrating the efficiency of GREACE in improving such a complex physiological trait. To understand the improved heat tolerance, genomes of HR50 and its wildtype strain DH5α were sequenced. Evenly distributed 361 mutations covering all mutation types were found in HR50. Closed material transportations, loose genome conformation, and possibly altered cell wall structure and transcription pattern were the main differences of HR50 compared with DH5α, which were speculated to be responsible for the improved heat tolerance. This work not only expanding our understanding of microbial heat tolerance, but also emphasizing that the in vivo continuous genome mutagenesis method, GREACE, is efficient in improving microbial complex physiological trait.
Copyright © 2015 Elsevier B.V. All rights reserved.

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Year:  2015        PMID: 25725322     DOI: 10.1016/j.nbt.2015.01.013

Source DB:  PubMed          Journal:  N Biotechnol        ISSN: 1871-6784            Impact factor:   5.079


  6 in total

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Authors:  Xuejiao Tian; Hao Chen; Hao Liu; Jihong Chen
Journal:  Appl Biochem Biotechnol       Date:  2021-09-14       Impact factor: 2.926

2.  Rationally designed perturbation factor drives evolution in Saccharomyces cerevisiae for industrial application.

Authors:  Xin Xu; Chunfeng Liu; Chengtuo Niu; Jinjing Wang; Feiyun Zheng; Yongxian Li; Qi Li
Journal:  J Ind Microbiol Biotechnol       Date:  2018-08-03       Impact factor: 3.346

3.  Improving Cadmium Resistance in Escherichia coli Through Continuous Genome Evolution.

Authors:  Weitong Qin; Jintong Zhao; Xiaoxia Yu; Xiaoqing Liu; Xiaoyu Chu; Jian Tian; Ningfeng Wu
Journal:  Front Microbiol       Date:  2019-02-20       Impact factor: 5.640

Review 4.  Intelligent host engineering for metabolic flux optimisation in biotechnology.

Authors:  Lachlan J Munro; Douglas B Kell
Journal:  Biochem J       Date:  2021-10-29       Impact factor: 3.857

5.  Biosensor-Coupled In Vivo Mutagenesis and Omics Analysis Reveals Reduced Lysine and Arginine Synthesis To Improve Malonyl-Coenzyme A Flux in Saccharomyces cerevisiae.

Authors:  Chenxi Qiu; Mingtao Huang; Yishan Hou; Huilin Tao; Jianzhi Zhao; Yu Shen; Xiaoming Bao; Qingsheng Qi; Jin Hou
Journal:  mSystems       Date:  2022-03-01       Impact factor: 7.324

Review 6.  Targeted mutagenesis: A sniper-like diversity generator in microbial engineering.

Authors:  Xiang Zheng; Xin-Hui Xing; Chong Zhang
Journal:  Synth Syst Biotechnol       Date:  2017-07-14
  6 in total

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