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Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor
FixK(2) is a CRP/FNR-type transcription factor that plays a central role in a sophisticated regulatory network for the anoxic, microoxic and symbiotic lifestyles of the soybean endosymbiont Bradyrhizobium diazoefficiens. Aside from the balanced expression of the fixK(2) gene under microoxic conditio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104804/ https://www.ncbi.nlm.nih.gov/pubmed/35563511 http://dx.doi.org/10.3390/ijms23095117 |
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author | Parejo, Sergio Cabrera, Juan J. Jiménez-Leiva, Andrea Tomás-Gallardo, Laura Bedmar, Eulogio J. Gates, Andrew J. Mesa, Socorro |
author_facet | Parejo, Sergio Cabrera, Juan J. Jiménez-Leiva, Andrea Tomás-Gallardo, Laura Bedmar, Eulogio J. Gates, Andrew J. Mesa, Socorro |
author_sort | Parejo, Sergio |
collection | PubMed |
description | FixK(2) is a CRP/FNR-type transcription factor that plays a central role in a sophisticated regulatory network for the anoxic, microoxic and symbiotic lifestyles of the soybean endosymbiont Bradyrhizobium diazoefficiens. Aside from the balanced expression of the fixK(2) gene under microoxic conditions (induced by the two-component regulatory system FixLJ and negatively auto-repressed), FixK(2) activity is posttranslationally controlled by proteolysis, and by the oxidation of a singular cysteine residue (C183) near its DNA-binding domain. To simulate the permanent oxidation of FixK(2), we replaced C183 for aspartic acid. Purified C183D FixK(2) protein showed both low DNA binding and in vitro transcriptional activation from the promoter of the fixNOQP operon, required for respiration under symbiosis. However, in a B. diazoefficiens strain coding for C183D FixK(2), expression of a fixNOQP’-‘lacZ fusion was similar to that in the wild type, when both strains were grown microoxically. The C183D FixK(2) encoding strain also showed a wild-type phenotype in symbiosis with soybeans, and increased fixK(2) gene expression levels and FixK(2) protein abundance in cells. These two latter observations, together with the global transcriptional profile of the microoxically cultured C183D FixK(2) encoding strain, suggest the existence of a finely tuned regulatory strategy to counterbalance the oxidation-mediated inactivation of FixK(2) in vivo. |
format | Online Article Text |
id | pubmed-9104804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91048042022-05-14 Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor Parejo, Sergio Cabrera, Juan J. Jiménez-Leiva, Andrea Tomás-Gallardo, Laura Bedmar, Eulogio J. Gates, Andrew J. Mesa, Socorro Int J Mol Sci Article FixK(2) is a CRP/FNR-type transcription factor that plays a central role in a sophisticated regulatory network for the anoxic, microoxic and symbiotic lifestyles of the soybean endosymbiont Bradyrhizobium diazoefficiens. Aside from the balanced expression of the fixK(2) gene under microoxic conditions (induced by the two-component regulatory system FixLJ and negatively auto-repressed), FixK(2) activity is posttranslationally controlled by proteolysis, and by the oxidation of a singular cysteine residue (C183) near its DNA-binding domain. To simulate the permanent oxidation of FixK(2), we replaced C183 for aspartic acid. Purified C183D FixK(2) protein showed both low DNA binding and in vitro transcriptional activation from the promoter of the fixNOQP operon, required for respiration under symbiosis. However, in a B. diazoefficiens strain coding for C183D FixK(2), expression of a fixNOQP’-‘lacZ fusion was similar to that in the wild type, when both strains were grown microoxically. The C183D FixK(2) encoding strain also showed a wild-type phenotype in symbiosis with soybeans, and increased fixK(2) gene expression levels and FixK(2) protein abundance in cells. These two latter observations, together with the global transcriptional profile of the microoxically cultured C183D FixK(2) encoding strain, suggest the existence of a finely tuned regulatory strategy to counterbalance the oxidation-mediated inactivation of FixK(2) in vivo. MDPI 2022-05-04 /pmc/articles/PMC9104804/ /pubmed/35563511 http://dx.doi.org/10.3390/ijms23095117 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Parejo, Sergio Cabrera, Juan J. Jiménez-Leiva, Andrea Tomás-Gallardo, Laura Bedmar, Eulogio J. Gates, Andrew J. Mesa, Socorro Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor |
title | Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor |
title_full | Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor |
title_fullStr | Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor |
title_full_unstemmed | Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor |
title_short | Fine-Tuning Modulation of Oxidation-Mediated Posttranslational Control of Bradyrhizobium diazoefficiens FixK(2) Transcription Factor |
title_sort | fine-tuning modulation of oxidation-mediated posttranslational control of bradyrhizobium diazoefficiens fixk(2) transcription factor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104804/ https://www.ncbi.nlm.nih.gov/pubmed/35563511 http://dx.doi.org/10.3390/ijms23095117 |
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