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Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23

De novo corrinoid biosynthesis represents one of the most complicated metabolic pathways in nature. Organohalide-respiring bacteria (OHRB) have developed different strategies to deal with their need of corrinoid, as it is an essential cofactor of reductive dehalogenases, the key enzymes in OHR metab...

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Autores principales: Rupakula, Aamani, Lu, Yue, Kruse, Thomas, Boeren, Sjef, Holliger, Christof, Smidt, Hauke, Maillard, Julien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285132/
https://www.ncbi.nlm.nih.gov/pubmed/25610435
http://dx.doi.org/10.3389/fmicb.2014.00751
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author Rupakula, Aamani
Lu, Yue
Kruse, Thomas
Boeren, Sjef
Holliger, Christof
Smidt, Hauke
Maillard, Julien
author_facet Rupakula, Aamani
Lu, Yue
Kruse, Thomas
Boeren, Sjef
Holliger, Christof
Smidt, Hauke
Maillard, Julien
author_sort Rupakula, Aamani
collection PubMed
description De novo corrinoid biosynthesis represents one of the most complicated metabolic pathways in nature. Organohalide-respiring bacteria (OHRB) have developed different strategies to deal with their need of corrinoid, as it is an essential cofactor of reductive dehalogenases, the key enzymes in OHR metabolism. In contrast to Dehalococcoides mccartyi, the genome of Dehalobacter restrictus strain PER-K23 contains a complete set of corrinoid biosynthetic genes, of which cbiH appears to be truncated and therefore non-functional, possibly explaining the corrinoid auxotrophy of this obligate OHRB. Comparative genomics within Dehalobacter spp. revealed that one (operon-2) of the five distinct corrinoid biosynthesis associated operons present in the genome of D. restrictus appeared to be present only in that particular strain, which encodes multiple members of corrinoid transporters and salvaging enzymes. Operon-2 was highly up-regulated upon corrinoid starvation both at the transcriptional (346-fold) and proteomic level (46-fold on average), in line with the presence of an upstream cobalamin riboswitch. Together, these data highlight the importance of this operon in corrinoid homeostasis in D. restrictus and the augmented salvaging strategy this bacterium adopted to cope with the need for this essential cofactor.
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spelling pubmed-42851322015-01-21 Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23 Rupakula, Aamani Lu, Yue Kruse, Thomas Boeren, Sjef Holliger, Christof Smidt, Hauke Maillard, Julien Front Microbiol Microbiology De novo corrinoid biosynthesis represents one of the most complicated metabolic pathways in nature. Organohalide-respiring bacteria (OHRB) have developed different strategies to deal with their need of corrinoid, as it is an essential cofactor of reductive dehalogenases, the key enzymes in OHR metabolism. In contrast to Dehalococcoides mccartyi, the genome of Dehalobacter restrictus strain PER-K23 contains a complete set of corrinoid biosynthetic genes, of which cbiH appears to be truncated and therefore non-functional, possibly explaining the corrinoid auxotrophy of this obligate OHRB. Comparative genomics within Dehalobacter spp. revealed that one (operon-2) of the five distinct corrinoid biosynthesis associated operons present in the genome of D. restrictus appeared to be present only in that particular strain, which encodes multiple members of corrinoid transporters and salvaging enzymes. Operon-2 was highly up-regulated upon corrinoid starvation both at the transcriptional (346-fold) and proteomic level (46-fold on average), in line with the presence of an upstream cobalamin riboswitch. Together, these data highlight the importance of this operon in corrinoid homeostasis in D. restrictus and the augmented salvaging strategy this bacterium adopted to cope with the need for this essential cofactor. Frontiers Media S.A. 2015-01-06 /pmc/articles/PMC4285132/ /pubmed/25610435 http://dx.doi.org/10.3389/fmicb.2014.00751 Text en Copyright © 2015 Rupakula, Lu, Kruse, Boeren, Holliger, Smidt and Maillard. 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) or licensor 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
Rupakula, Aamani
Lu, Yue
Kruse, Thomas
Boeren, Sjef
Holliger, Christof
Smidt, Hauke
Maillard, Julien
Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23
title Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23
title_full Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23
title_fullStr Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23
title_full_unstemmed Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23
title_short Functional genomics of corrinoid starvation in the organohalide-respiring bacterium Dehalobacter restrictus strain PER-K23
title_sort functional genomics of corrinoid starvation in the organohalide-respiring bacterium dehalobacter restrictus strain per-k23
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285132/
https://www.ncbi.nlm.nih.gov/pubmed/25610435
http://dx.doi.org/10.3389/fmicb.2014.00751
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