Literature DB >> 29802191

Experimental Evolution of Escherichia coli K-12 at High pH and with RpoS Induction.

Issam Hamdallah1,2, Nadia Torok1, Katarina M Bischof1, Nadim Majdalani2, Sriya Chadalavada1, Nonto Mdluli1, Kaitlin E Creamer1, Michelle Clark1, Chase Holdener1, Preston J Basting1, Susan Gottesman2, Joan L Slonczewski3.   

Abstract

Experimental evolution of Escherichia coli K-12 W3110 by serial dilutions for 2,200 generations at high pH extended the range of sustained growth from pH 9.0 to pH 9.3. pH 9.3-adapted isolates showed mutations in DNA-binding regulators and envelope proteins. One population showed an IS1 knockout of phoB (encoding the positive regulator of the phosphate regulon). A phoB::kanR knockout increased growth at high pH. phoB mutants are known to increase production of fermentation acids, which could enhance fitness at high pH. Mutations in pcnB [poly(A) polymerase] also increased growth at high pH. Three out of four populations showed deletions of torI, an inhibitor of TorR, which activates expression of torCAD (trimethylamine N-oxide respiration) at high pH. All populations showed point mutations affecting the stationary-phase sigma factor RpoS, either in the coding gene or in genes for regulators of RpoS expression. RpoS is required for survival at extremely high pH. In our microplate assay, rpoS deletion slightly decreased growth at pH 9.1. RpoS protein accumulated faster at pH 9 than at pH 7. The RpoS accumulation at high pH required the presence of one or more antiadaptors that block degradation (IraM, IraD, and IraP). Other genes with mutations after high-pH evolution encode regulators, such as those encoded by yobG (mgrB) (PhoPQ regulator), rpoN (nitrogen starvation sigma factor), malI, and purR, as well as envelope proteins, such as those encoded by ompT and yahO Overall, E. coli evolution at high pH selects for mutations in key transcriptional regulators, including phoB and the stationary-phase sigma factor RpoS.IMPORTANCEEscherichia coli in its native habitat encounters high-pH stress such as that of pancreatic secretions. Experimental evolution over 2,000 generations showed selection for mutations in regulatory factors, such as deletion of the phosphate regulator PhoB and mutations that alter the function of the global stress regulator RpoS. RpoS is induced at high pH via multiple mechanisms.
Copyright © 2018 American Society for Microbiology.

Entities:  

Keywords:  PhoB; RpoS; evolution; high pH

Mesh:

Substances:

Year:  2018        PMID: 29802191      PMCID: PMC6052260          DOI: 10.1128/AEM.00520-18

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  52 in total

1.  pH regulates genes for flagellar motility, catabolism, and oxidative stress in Escherichia coli K-12.

Authors:  Lisa M Maurer; Elizabeth Yohannes; Sandra S Bondurant; Michael Radmacher; Joan L Slonczewski
Journal:  J Bacteriol       Date:  2005-01       Impact factor: 3.490

2.  Starvation for different nutrients in Escherichia coli results in differential modulation of RpoS levels and stability.

Authors:  Mark J Mandel; Thomas J Silhavy
Journal:  J Bacteriol       Date:  2005-01       Impact factor: 3.490

Review 3.  Hfq structure, function and ligand binding.

Authors:  Richard G Brennan; Todd M Link
Journal:  Curr Opin Microbiol       Date:  2007-03-28       Impact factor: 7.934

4.  SspA is required for acid resistance in stationary phase by downregulation of H-NS in Escherichia coli.

Authors:  Anne-Marie Hansen; Yu Qiu; Norman Yeh; Frederick R Blattner; Tim Durfee; Ding Jun Jin
Journal:  Mol Microbiol       Date:  2005-05       Impact factor: 3.501

5.  Effect of acidic condition on the metabolic regulation of Escherichia coli and its phoB mutant.

Authors:  Lolo Wal Marzan; Chowdhury Mohammad Monirul Hasan; Kazuyuki Shimizu
Journal:  Arch Microbiol       Date:  2012-12-30       Impact factor: 2.552

Review 6.  Recombineering: genetic engineering in bacteria using homologous recombination.

Authors:  Lynn C Thomason; James A Sawitzke; Xintian Li; Nina Costantino; Donald L Court
Journal:  Curr Protoc Mol Biol       Date:  2014-04-14

7.  pH-dependent expression of periplasmic proteins and amino acid catabolism in Escherichia coli.

Authors:  Lauren M Stancik; Dawn M Stancik; Brian Schmidt; D Michael Barnhart; Yuliya N Yoncheva; Joan L Slonczewski
Journal:  J Bacteriol       Date:  2002-08       Impact factor: 3.490

8.  Anticipating an alkaline stress through the Tor phosphorelay system in Escherichia coli.

Authors:  Christophe Bordi; Laurence Théraulaz; Vincent Méjean; Cécile Jourlin-Castelli
Journal:  Mol Microbiol       Date:  2003-04       Impact factor: 3.501

9.  Culture volume and vessel affect long-term survival, mutation frequency, and oxidative stress of Escherichia coli.

Authors:  Karin E Kram; Steven E Finkel
Journal:  Appl Environ Microbiol       Date:  2013-12-27       Impact factor: 4.792

10.  Oxygen limitation modulates pH regulation of catabolism and hydrogenases, multidrug transporters, and envelope composition in Escherichia coli K-12.

Authors:  Everett T Hayes; Jessica C Wilks; Piero Sanfilippo; Elizabeth Yohannes; Daniel P Tate; Brian D Jones; Michael D Radmacher; Sandra S BonDurant; Joan L Slonczewski
Journal:  BMC Microbiol       Date:  2006-10-06       Impact factor: 3.605

View more
  3 in total

Review 1.  Trouble is coming: Signaling pathways that regulate general stress responses in bacteria.

Authors:  Susan Gottesman
Journal:  J Biol Chem       Date:  2019-06-13       Impact factor: 5.157

2.  Visualizing the pH in Escherichia coli Colonies via the Sensor Protein mCherryEA Allows High-Throughput Screening of Mutant Libraries.

Authors:  Fabian Stefan Franz Hartmann; Tamara Weiß; Jing Shen; Dóra Smahajcsik; Simonas Savickas; Gerd Michael Seibold
Journal:  mSystems       Date:  2022-04-18       Impact factor: 7.324

Review 3.  Experimental Challenges for Reduced Genomes: The Cell Model Escherichia coli.

Authors:  Masaomi Kurokawa; Bei-Wen Ying
Journal:  Microorganisms       Date:  2019-12-18
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.