Factors affecting redox potential and differential sensitivity of SoxR to redox‐active compounds. Issue 5 (12th June 2015)
- Record Type:
- Journal Article
- Title:
- Factors affecting redox potential and differential sensitivity of SoxR to redox‐active compounds. Issue 5 (12th June 2015)
- Main Title:
- Factors affecting redox potential and differential sensitivity of SoxR to redox‐active compounds
- Authors:
- Lee, Kang‐Lok
Singh, Atul K.
Heo, Lim
Seok, Chaok
Roe, Jung‐Hye - Abstract:
- <abstract abstract-type="main"> <title>Summary</title> <p>SoxR is a [2Fe‐2S]‐containing sensor‐regulator, which is activated through oxidation by redox‐active compounds (RACs). SoxRs show differential sensitivity to RACs, partly due to different redox potentials, such that <italic>E</italic><italic>scherichia coli</italic> (Ec) SoxR with lower potential respond to broader range of RACs than <italic>S</italic><italic>treptomyces coelicolor</italic> (Sc) SoxR. In <italic>S</italic><italic>. coelicolor</italic>, the RACs that do not activate ScSoxR did not inhibit growth, suggesting that ScSoxR is tuned to respond to growth‐inhibitory RACs. Based on sequence comparison and mutation studies, two critical amino acids around the [2Fe‐2S] binding site were proposed as key determinants of sensitivity. ScSoxR‐like mutation (R127L/P131V) in EcSoxR changed its sensitivity profile as ScSoxR, whereas EcSoxR‐like mutation (L126R/V130P) in ScSoxR caused relaxed response. In accordance, the redox potentials of EcSoxR<sup>R</sup><sup>127</sup><sup>L</sup><sup>/</sup><sup>P</sup><sup>131</sup><sup>V</sup> and ScSoxR<sup>L126R/V130P</sup> were estimated to be −192 ± 8 mV and −273 ± 10 mV, respectively, approaching that of ScSoxR (−185 mV) and EcSoxR (−290 mV). Molecular dynamics simulations revealed that the R127L and P131V substitutions in EcSoxR caused more electropositive environment around [2Fe‐2S], making it harder to get oxidized. This reveals a mechanism to modulate redox‐potential in<abstract abstract-type="main"> <title>Summary</title> <p>SoxR is a [2Fe‐2S]‐containing sensor‐regulator, which is activated through oxidation by redox‐active compounds (RACs). SoxRs show differential sensitivity to RACs, partly due to different redox potentials, such that <italic>E</italic><italic>scherichia coli</italic> (Ec) SoxR with lower potential respond to broader range of RACs than <italic>S</italic><italic>treptomyces coelicolor</italic> (Sc) SoxR. In <italic>S</italic><italic>. coelicolor</italic>, the RACs that do not activate ScSoxR did not inhibit growth, suggesting that ScSoxR is tuned to respond to growth‐inhibitory RACs. Based on sequence comparison and mutation studies, two critical amino acids around the [2Fe‐2S] binding site were proposed as key determinants of sensitivity. ScSoxR‐like mutation (R127L/P131V) in EcSoxR changed its sensitivity profile as ScSoxR, whereas EcSoxR‐like mutation (L126R/V130P) in ScSoxR caused relaxed response. In accordance, the redox potentials of EcSoxR<sup>R</sup><sup>127</sup><sup>L</sup><sup>/</sup><sup>P</sup><sup>131</sup><sup>V</sup> and ScSoxR<sup>L126R/V130P</sup> were estimated to be −192 ± 8 mV and −273 ± 10 mV, respectively, approaching that of ScSoxR (−185 mV) and EcSoxR (−290 mV). Molecular dynamics simulations revealed that the R127L and P131V substitutions in EcSoxR caused more electropositive environment around [2Fe‐2S], making it harder to get oxidized. This reveals a mechanism to modulate redox‐potential in [Fe‐S]‐containing sensors by point mutations and to evolve a sensor with differential sensitivity to achieve optimal cellular physiology.</p> </abstract> … (more)
- Is Part Of:
- Molecular microbiology. Volume 97:Issue 5(2015)
- Journal:
- Molecular microbiology
- Issue:
- Volume 97:Issue 5(2015)
- Issue Display:
- Volume 97, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 97
- Issue:
- 5
- Issue Sort Value:
- 2015-0097-0005-0000
- Page Start:
- 808
- Page End:
- 821
- Publication Date:
- 2015-06-12
- Subjects:
- Molecular microbiology -- Periodicals
572.829 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=mmi&close=2003#C2003 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2958 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/mmi.13068 ↗
- Languages:
- English
- ISSNs:
- 0950-382X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817960
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4347.xml