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Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth
Pseudomonas aeruginosa is a major pathogenic bacterium in chronic infections and is a model organism for studying biofilms. P. aeruginosa is considered an aerobic bacterium, but in the presence of nitrate, it also grows in anaerobic conditions. Oxygen diffusion through the biofilm generates metaboli...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5962746/ https://www.ncbi.nlm.nih.gov/pubmed/29867886 http://dx.doi.org/10.3389/fmicb.2018.00986 |
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author | Crespo, Anna Blanco-Cabra, Núria Torrents, Eduard |
author_facet | Crespo, Anna Blanco-Cabra, Núria Torrents, Eduard |
author_sort | Crespo, Anna |
collection | PubMed |
description | Pseudomonas aeruginosa is a major pathogenic bacterium in chronic infections and is a model organism for studying biofilms. P. aeruginosa is considered an aerobic bacterium, but in the presence of nitrate, it also grows in anaerobic conditions. Oxygen diffusion through the biofilm generates metabolic and genetic diversity in P. aeruginosa growth, such as in ribonucleotide reductase activity. These essential enzymes are necessary for DNA synthesis and repair. Oxygen availability determines the activity of the three-ribonucleotide reductase (RNR) classes. Class II and III RNRs are active in the absence of oxygen; however, class II RNRs, which are important in P. aeruginosa biofilm growth, require a vitamin B(12) cofactor for their enzymatic activity. In this work, we elucidated the conditions in which class II RNRs are active due to vitamin B(12) concentration constraints (biosynthesis or environmental availability). We demonstrated that increased vitamin B(12) levels during aerobic, stationary and biofilm growth activate class II RNR activity. We also established that the cobN gene is essentially responsible for B(12) biosynthesis under planktonic and biofilm growth. Our results unravel the mechanisms of dNTP synthesis by P. aeruginosa during biofilm growth, which appear to depend on the bacterial strain (laboratory-type or clinical isolate). |
format | Online Article Text |
id | pubmed-5962746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59627462018-06-04 Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth Crespo, Anna Blanco-Cabra, Núria Torrents, Eduard Front Microbiol Microbiology Pseudomonas aeruginosa is a major pathogenic bacterium in chronic infections and is a model organism for studying biofilms. P. aeruginosa is considered an aerobic bacterium, but in the presence of nitrate, it also grows in anaerobic conditions. Oxygen diffusion through the biofilm generates metabolic and genetic diversity in P. aeruginosa growth, such as in ribonucleotide reductase activity. These essential enzymes are necessary for DNA synthesis and repair. Oxygen availability determines the activity of the three-ribonucleotide reductase (RNR) classes. Class II and III RNRs are active in the absence of oxygen; however, class II RNRs, which are important in P. aeruginosa biofilm growth, require a vitamin B(12) cofactor for their enzymatic activity. In this work, we elucidated the conditions in which class II RNRs are active due to vitamin B(12) concentration constraints (biosynthesis or environmental availability). We demonstrated that increased vitamin B(12) levels during aerobic, stationary and biofilm growth activate class II RNR activity. We also established that the cobN gene is essentially responsible for B(12) biosynthesis under planktonic and biofilm growth. Our results unravel the mechanisms of dNTP synthesis by P. aeruginosa during biofilm growth, which appear to depend on the bacterial strain (laboratory-type or clinical isolate). Frontiers Media S.A. 2018-05-15 /pmc/articles/PMC5962746/ /pubmed/29867886 http://dx.doi.org/10.3389/fmicb.2018.00986 Text en Copyright © 2018 Crespo, Blanco-Cabra and Torrents. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Crespo, Anna Blanco-Cabra, Núria Torrents, Eduard Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth |
title | Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth |
title_full | Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth |
title_fullStr | Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth |
title_full_unstemmed | Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth |
title_short | Aerobic Vitamin B(12) Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth |
title_sort | aerobic vitamin b(12) biosynthesis is essential for pseudomonas aeruginosa class ii ribonucleotide reductase activity during planktonic and biofilm growth |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5962746/ https://www.ncbi.nlm.nih.gov/pubmed/29867886 http://dx.doi.org/10.3389/fmicb.2018.00986 |
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