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Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11

Isoprene monooxygenase (IsoMO, encoded by isoABCDEF) initiates the oxidation of the climate-active gas isoprene, with the genes isoGHIJ and aldH nearly always found adjacent to isoABCDEF in extant and metagenome-derived isoprene degraders. The roles of isoGHIJ and aldH are uncertain, although each i...

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Autores principales: Rix, Gregory D., Sims, Leanne P., Dawson, Robin A., Williamson, Gordon, Bryant, Yasmin, Crombie, Andrew T., Murrell, J. Colin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057887/
https://www.ncbi.nlm.nih.gov/pubmed/36840579
http://dx.doi.org/10.1128/aem.02122-22
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author Rix, Gregory D.
Sims, Leanne P.
Dawson, Robin A.
Williamson, Gordon
Bryant, Yasmin
Crombie, Andrew T.
Murrell, J. Colin
author_facet Rix, Gregory D.
Sims, Leanne P.
Dawson, Robin A.
Williamson, Gordon
Bryant, Yasmin
Crombie, Andrew T.
Murrell, J. Colin
author_sort Rix, Gregory D.
collection PubMed
description Isoprene monooxygenase (IsoMO, encoded by isoABCDEF) initiates the oxidation of the climate-active gas isoprene, with the genes isoGHIJ and aldH nearly always found adjacent to isoABCDEF in extant and metagenome-derived isoprene degraders. The roles of isoGHIJ and aldH are uncertain, although each is essential to isoprene degradation. We report here the characterization of these proteins from two model isoprene degraders, Rhodococcus sp. strain AD45 and Variovorax sp. strain WS11. The genes isoHIJ and aldH from Variovorax and aldH from Rhodococcus were expressed individually in Escherichia coli as maltose binding protein fusions to overcome issues of insolubility. The activity of two glutathione S-transferases from Variovorax, IsoI and IsoJ was assessed with model substrates, and the conversion of epoxyisoprene to the intermediate 1-hydroxy-2-glutathionyl-2-methyl-3-butene (HGMB) was demonstrated. The next step of the isoprene metabolic pathway of Variovorax is catalyzed by the dehydrogenase IsoH, resulting in the conversion of HGMB to 2-glutathionyl-2-methyl-3-butenoic acid (GMBA). The aldehyde dehydrogenases (AldH) from Variovorax and Rhodococcus were examined with a variety of aldehydes, with both exhibiting maximum activity with butanal. AldH significantly increased the rate of production of NADH when added to the IsoH-catalyzed conversion of HGMB to GMBA (via GMB), suggesting a synergistic role for AldH in the isoprene metabolic pathway. An in silico analysis of IsoG revealed that this protein, which is essential for isoprene metabolism in Variovorax, is an enzyme of the formyl CoA-transferase family and is predicted to catalyze the formation of a GMBA-CoA thioester as an intermediate in the isoprene oxidation pathway. IMPORTANCE Isoprene is a climate-active gas, largely produced by trees, which is released from the biosphere in amounts equivalent to those of methane and all other volatile organic compounds combined. Bacteria found in many environments, including soils and on the surface of leaves of isoprene-producing trees, can grow on isoprene and thus may represent a significant biological sink for this globally significant volatile compound and remove isoprene before it escapes to the atmosphere, thus reducing its potency as a climate-active gas. The initial oxidation of isoprene by bacteria is mediated by isoprene monooxygenase encoded by the genes isoABCDEF. In isoprene-degrading bacteria, a second gene cluster, isoGHIJ, is also present, although the exact role in isoprene degradation by the proteins encoded by these genes is uncertain. This investigation sheds new light on the roles of these proteins in the isoprene oxidation pathway in two model isoprene-degrading bacteria of the genera Rhodococcus and Variovorax.
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spelling pubmed-100578872023-03-30 Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11 Rix, Gregory D. Sims, Leanne P. Dawson, Robin A. Williamson, Gordon Bryant, Yasmin Crombie, Andrew T. Murrell, J. Colin Appl Environ Microbiol Environmental Microbiology Isoprene monooxygenase (IsoMO, encoded by isoABCDEF) initiates the oxidation of the climate-active gas isoprene, with the genes isoGHIJ and aldH nearly always found adjacent to isoABCDEF in extant and metagenome-derived isoprene degraders. The roles of isoGHIJ and aldH are uncertain, although each is essential to isoprene degradation. We report here the characterization of these proteins from two model isoprene degraders, Rhodococcus sp. strain AD45 and Variovorax sp. strain WS11. The genes isoHIJ and aldH from Variovorax and aldH from Rhodococcus were expressed individually in Escherichia coli as maltose binding protein fusions to overcome issues of insolubility. The activity of two glutathione S-transferases from Variovorax, IsoI and IsoJ was assessed with model substrates, and the conversion of epoxyisoprene to the intermediate 1-hydroxy-2-glutathionyl-2-methyl-3-butene (HGMB) was demonstrated. The next step of the isoprene metabolic pathway of Variovorax is catalyzed by the dehydrogenase IsoH, resulting in the conversion of HGMB to 2-glutathionyl-2-methyl-3-butenoic acid (GMBA). The aldehyde dehydrogenases (AldH) from Variovorax and Rhodococcus were examined with a variety of aldehydes, with both exhibiting maximum activity with butanal. AldH significantly increased the rate of production of NADH when added to the IsoH-catalyzed conversion of HGMB to GMBA (via GMB), suggesting a synergistic role for AldH in the isoprene metabolic pathway. An in silico analysis of IsoG revealed that this protein, which is essential for isoprene metabolism in Variovorax, is an enzyme of the formyl CoA-transferase family and is predicted to catalyze the formation of a GMBA-CoA thioester as an intermediate in the isoprene oxidation pathway. IMPORTANCE Isoprene is a climate-active gas, largely produced by trees, which is released from the biosphere in amounts equivalent to those of methane and all other volatile organic compounds combined. Bacteria found in many environments, including soils and on the surface of leaves of isoprene-producing trees, can grow on isoprene and thus may represent a significant biological sink for this globally significant volatile compound and remove isoprene before it escapes to the atmosphere, thus reducing its potency as a climate-active gas. The initial oxidation of isoprene by bacteria is mediated by isoprene monooxygenase encoded by the genes isoABCDEF. In isoprene-degrading bacteria, a second gene cluster, isoGHIJ, is also present, although the exact role in isoprene degradation by the proteins encoded by these genes is uncertain. This investigation sheds new light on the roles of these proteins in the isoprene oxidation pathway in two model isoprene-degrading bacteria of the genera Rhodococcus and Variovorax. American Society for Microbiology 2023-02-22 /pmc/articles/PMC10057887/ /pubmed/36840579 http://dx.doi.org/10.1128/aem.02122-22 Text en Copyright © 2023 Rix et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Environmental Microbiology
Rix, Gregory D.
Sims, Leanne P.
Dawson, Robin A.
Williamson, Gordon
Bryant, Yasmin
Crombie, Andrew T.
Murrell, J. Colin
Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11
title Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11
title_full Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11
title_fullStr Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11
title_full_unstemmed Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11
title_short Analysis of Essential Isoprene Metabolic Pathway Proteins in Variovorax sp. Strain WS11
title_sort analysis of essential isoprene metabolic pathway proteins in variovorax sp. strain ws11
topic Environmental Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057887/
https://www.ncbi.nlm.nih.gov/pubmed/36840579
http://dx.doi.org/10.1128/aem.02122-22
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