Literature DB >> 16771669

Ribonucleotide reductases: influence of environment on synthesis and activity.

Stéphanie Gon1, Jon Beckwith.   

Abstract

Ribonucleotide reductases (RNRs) are enzymes that provide deoxyribonucleotides (dNTPs), the building blocks required for de novo DNA synthesis and repair. They are found in all organisms from prokaryotes to eukaryotes. Interestingly, in the microbial world, several organisms possess the genes encoding two, or even three different RNRs that present different structures and allosteric regulation. The finding of an increasing number of bacterial species that possess more than one RNR might suggest particular functions for these enzymes in different growth conditions. Recent support for this proposal comes from studies indicating that expression and activity of the different RNRs depends on the environment. The oxygen content as well as the redox and oxidative stresses regulate RNR activity and synthesis in various organisms. This regulation has a direct consequence on dNTP pools. An excess of dNTP pools that leads to misincorporation of dNTPs results in genetic abnormalities in eukaryotes as in prokaryotes. In contrast, increased dNTP concentrations help cells to survive under conditions where DNA has been damaged. Hence the use of different RNRs in response to various environmental conditions allows the cell to regulate the amount precisely of dNTP in both a positive and negative manner so that enough, yet not excessive, dNTPs are synthesized.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16771669     DOI: 10.1089/ars.2006.8.773

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  15 in total

Review 1.  Manganese uptake and streptococcal virulence.

Authors:  Bart A Eijkelkamp; Christopher A McDevitt; Todd Kitten
Journal:  Biometals       Date:  2015-02-05       Impact factor: 2.949

2.  Peroxide stimulon and role of PerR in group A Streptococcus.

Authors:  Renata Grifantini; Chadia Toukoki; Annalisa Colaprico; Ioannis Gryllos
Journal:  J Bacteriol       Date:  2011-09-23       Impact factor: 3.490

3.  Structural basis on the dityrosyl-diiron radical cluster and the functional differences of human ribonucleotide reductase small subunits hp53R2 and hRRM2.

Authors:  Bingsen Zhou; Leila Su; Yate-Ching Yuan; Frank Un; Norby Wang; Madhukar Patel; Bixin Xi; Shuya Hu; Yun Yen
Journal:  Mol Cancer Ther       Date:  2010-05-18       Impact factor: 6.261

4.  Mutations at several loci cause increased expression of ribonucleotide reductase in Escherichia coli.

Authors:  Morgan Anne Feeney; Na Ke; Jon Beckwith
Journal:  J Bacteriol       Date:  2012-01-13       Impact factor: 3.490

5.  Transcriptomic response of Escherichia coli O157:H7 to oxidative stress.

Authors:  Siyun Wang; Kaiping Deng; Sam Zaremba; Xiangyu Deng; Chiahui Lin; Qian Wang; Mary Lou Tortorello; Wei Zhang
Journal:  Appl Environ Microbiol       Date:  2009-08-07       Impact factor: 4.792

6.  Increase in dNTP pool size during the DNA damage response plays a key role in spontaneous and induced-mutagenesis in Escherichia coli.

Authors:  Stéphanie Gon; Rita Napolitano; Walter Rocha; Stéphane Coulon; Robert P Fuchs
Journal:  Proc Natl Acad Sci U S A       Date:  2011-11-14       Impact factor: 11.205

7.  Functional analysis of the Streptomyces coelicolor NrdR ATP-cone domain: role in nucleotide binding, oligomerization, and DNA interactions.

Authors:  Inna Grinberg; Tatyana Shteinberg; A Quamrul Hassan; Yair Aharonowitz; Ilya Borovok; Gerald Cohen
Journal:  J Bacteriol       Date:  2008-12-01       Impact factor: 3.490

8.  NrdI, a flavodoxin involved in maintenance of the diferric-tyrosyl radical cofactor in Escherichia coli class Ib ribonucleotide reductase.

Authors:  Joseph A Cotruvo; JoAnne Stubbe
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-17       Impact factor: 11.205

Review 9.  Role of reactive oxygen species in antibiotic action and resistance.

Authors:  Daniel J Dwyer; Michael A Kohanski; James J Collins
Journal:  Curr Opin Microbiol       Date:  2009-07-31       Impact factor: 7.934

10.  Loss of yeast peroxiredoxin Tsa1p induces genome instability through activation of the DNA damage checkpoint and elevation of dNTP levels.

Authors:  Hei-Man Vincent Tang; Kam-Leung Siu; Chi-Ming Wong; Dong-Yan Jin
Journal:  PLoS Genet       Date:  2009-10-23       Impact factor: 5.917

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.