Cargando…

Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis

The Streptomyces avermitilis genome encodes a putative high‐affinity [NiFe]‐hydrogenase conferring the ability to oxidize tropospheric H(2) in mature spores. Here, we used a combination of transcriptomic and mutagenesis approaches to shed light on the potential ecophysiological role of the enzyme. F...

Descripción completa

Detalles Bibliográficos
Autores principales: Liot, Quentin, Constant, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767420/
https://www.ncbi.nlm.nih.gov/pubmed/26541261
http://dx.doi.org/10.1002/mbo3.310
_version_ 1782417809843683328
author Liot, Quentin
Constant, Philippe
author_facet Liot, Quentin
Constant, Philippe
author_sort Liot, Quentin
collection PubMed
description The Streptomyces avermitilis genome encodes a putative high‐affinity [NiFe]‐hydrogenase conferring the ability to oxidize tropospheric H(2) in mature spores. Here, we used a combination of transcriptomic and mutagenesis approaches to shed light on the potential ecophysiological role of the enzyme. First, S. avermitilis was either exposed to low or hydrogenase‐saturating levels of H(2) to investigate the impact of H(2) on spore transcriptome. In total, 1293 genes were differentially expressed, with 1127 and 166 showing lower and higher expression under elevated H(2) concentration, respectively. High H(2) exposure lowered the expression of the Sec protein secretion pathway and ATP‐binding cassette‐transporters, with increased expression of genes encoding proteins directing carbon metabolism toward sugar anabolism and lower expression of NADH dehydrogenase in the respiratory chain. Overall, the expression of relA responsible for the synthesis of the pleiotropic alarmone ppGpp decreased upon elevated H(2) exposure, which likely explained the reduced expression of antibiotic synthesis and stress response genes. Finally, deletion of hhySL genes resulted in a loss of H(2) uptake activity and a dramatic loss of viability in spores. We propose that H(2) is restricted to support the seed bank of Streptomyces under a unique survival–mixotrophic energy mode and discuss important ecological implications of this finding.
format Online
Article
Text
id pubmed-4767420
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-47674202016-03-07 Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis Liot, Quentin Constant, Philippe Microbiologyopen Original Research The Streptomyces avermitilis genome encodes a putative high‐affinity [NiFe]‐hydrogenase conferring the ability to oxidize tropospheric H(2) in mature spores. Here, we used a combination of transcriptomic and mutagenesis approaches to shed light on the potential ecophysiological role of the enzyme. First, S. avermitilis was either exposed to low or hydrogenase‐saturating levels of H(2) to investigate the impact of H(2) on spore transcriptome. In total, 1293 genes were differentially expressed, with 1127 and 166 showing lower and higher expression under elevated H(2) concentration, respectively. High H(2) exposure lowered the expression of the Sec protein secretion pathway and ATP‐binding cassette‐transporters, with increased expression of genes encoding proteins directing carbon metabolism toward sugar anabolism and lower expression of NADH dehydrogenase in the respiratory chain. Overall, the expression of relA responsible for the synthesis of the pleiotropic alarmone ppGpp decreased upon elevated H(2) exposure, which likely explained the reduced expression of antibiotic synthesis and stress response genes. Finally, deletion of hhySL genes resulted in a loss of H(2) uptake activity and a dramatic loss of viability in spores. We propose that H(2) is restricted to support the seed bank of Streptomyces under a unique survival–mixotrophic energy mode and discuss important ecological implications of this finding. John Wiley and Sons Inc. 2015-11-05 /pmc/articles/PMC4767420/ /pubmed/26541261 http://dx.doi.org/10.1002/mbo3.310 Text en © 2015 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Liot, Quentin
Constant, Philippe
Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis
title Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis
title_full Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis
title_fullStr Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis
title_full_unstemmed Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis
title_short Breathing air to save energy – new insights into the ecophysiological role of high‐affinity [NiFe]‐hydrogenase in Streptomyces avermitilis
title_sort breathing air to save energy – new insights into the ecophysiological role of high‐affinity [nife]‐hydrogenase in streptomyces avermitilis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767420/
https://www.ncbi.nlm.nih.gov/pubmed/26541261
http://dx.doi.org/10.1002/mbo3.310
work_keys_str_mv AT liotquentin breathingairtosaveenergynewinsightsintotheecophysiologicalroleofhighaffinitynifehydrogenaseinstreptomycesavermitilis
AT constantphilippe breathingairtosaveenergynewinsightsintotheecophysiologicalroleofhighaffinitynifehydrogenaseinstreptomycesavermitilis