Peering down the sink: A review of isoprene metabolism by bacteria.


Journal

Environmental microbiology
ISSN: 1462-2920
Titre abrégé: Environ Microbiol
Pays: England
ID NLM: 100883692

Informations de publication

Date de publication:
04 2023
Historique:
received: 03 11 2022
accepted: 21 12 2022
medline: 4 4 2023
pubmed: 26 12 2022
entrez: 25 12 2022
Statut: ppublish

Résumé

Isoprene (2-methyl-1,3-butadiene) is emitted to the atmosphere each year in sufficient quantities to rival methane (>500 Tg C yr

Identifiants

pubmed: 36567445
doi: 10.1111/1462-2920.16325
doi:

Substances chimiques

isoprene 0A62964IBU
Hemiterpenes 0
Butadienes 0
Pentanes 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

786-799

Informations de copyright

© 2022 The Authors. Environmental Microbiology published by Applied Microbiology International and John Wiley & Sons Ltd.

Références

Acuña Alvarez, L., Exton, D.A., Timmis, K.N., Suggett, D.J. & McGenity, T.J. (2009) Characterization of marine isoprene-degrading communities. Environmental Microbiology, 11, 3280-3291.
Altschul, S.F., Gish, W., Miller, W., Myers, E.W. & Lipman, D.J. (1990) Basic local alignment search tool. Journal of Molecular Biology, 215, 403-410.
Bäck, J., Aaltonen, H., Hellén, H., Kajos, M.K., Patokoski, J., Taipale, R. et al. (2010) Variable emissions of microbial volatile organic compounds (MVOCs) from root-associated fungi isolated from scots pine. Atmospheric Environment, 44, 3651-3659.
Broadgate, W.J., Malin, G., Küpper, F.C., Thompson, A. & Liss, P.S. (2004) Isoprene and other non-methane hydrocarbons from seaweeds: a source of reactive hydrocarbons to the atmosphere. Marine Chemistry, 88, 61-73.
Carrión, O., Gibson, L., Elias, D.M.O., McNamara, N.P., Van Alen, T.A., Op Den Camp, H.J.M. et al. (2020) Diversity of isoprene-degrading bacteria in phyllosphere and soil communities from a high isoprene-emitting environment: a Malaysian oil palm plantation. Microbiome, 8, 81. Available from: https://doi.org/10.1186/s40168-020-00860-7
Carrión, O., Larke-Mejía, N.L., Gibson, L., Farhan Ul Haque, M., Ramiro-garcía, J., McGenity, T.J. et al. (2018) Gene probing reveals the widespread distribution, diversity and abundance of isoprene-degrading bacteria in the environment. Microbiome, 6, 219. Available from: https://doi.org/10.1186/s40168-018-0607-0
Carrión, O., McGenity, T.J. & Murrell, J.C. (2020) Molecular ecology of isoprene-degrading bacteria. Microorganisms, 8(7), 967. Available from: https://doi.org/10.3390/microorganisms8070967
Cheung, S., McCarl, V., Holmes, A.J., Coleman, N.V. & Rutledge, P.J. (2013) Substrate range and enantioselectivity of epoxidation reactions mediated by the ethene-oxidising Mycobacterium strain NBB4. Applied Microbiology and Biotechnology, 97, 1131-1140.
Cleveland, C. & Yavitt, J. (1997) Consumption of atmospheric isoprene in soil. Geophysical Research Letters, 24, 2379-2382.
Conrad, R.S., Massey, L.K. & Sokatch, J.R. (1974) D and L isoleucine metabolism and regulation of their pathways in Pseudomonas putida. Journal of Bacteriology, 118, 103-111.
Crombie, A.T. (2011) Metabolism of methane and propane and the role of the glyoxylate bypass enzymes in Methylocella silvestris BL2. PhD Thesis. UK: University Warwick.
Crombie, A.T., El Khawand, M., Rhodius, V.A., Fengler, K.A., Miller, M.C., Whited, G.M. et al. (2015) Regulation of plasmid-encoded isoprene metabolism in Rhodococcus, a representative of an important link in the global isoprene cycle. Environmental Microbiology, 17, 3314-3329.
Crombie, A.T., Larke-Mejia, N.L., Emery, H., Dawson, R.A., Pratscher, J. & Murphy, G.P. (2018) Poplar phyllosphere harbors disparate isoprene-degrading bacteria. Proceedings of the National Academy of Sciences, 115, 13081-13086.
Dawson, R.A., Crombie, A.T., Pichon, P., Mcgenity, T.J. & Murrell, J.C. (2021) The microbiology of isoprene cycling in aquatic ecosystems. Aquatic Microbial Ecology, 87, 79-98.
Dawson, R.A., Larke-Mejía, N.L., Crombie, A.T., Farhan Ul Haque, M. & Murrell, J.C. (2020) Isoprene oxidation by the gram-negative model bacterium Variovorax sp. WS11. Microorganisms, 8(3), 349. Available from: https://doi.org/10.3390/microorganisms8030349
Dawson, R.A., Rix, G.D., Crombie, A.T. & Murrell, J.C. (2022) Omics-guided prediction of the pathway for metabolism of isoprene by Variovorax sp. WS11. Environmental Microbiology, 24, 5151-5164.
DeMaster, E.G. & Nagasawa, H.T. (1978) Isoprene, an endogenous constituent of human alveolar air with a diurnal pattern of excretion. Life Sciences, 22, 91-97.
Ekberg, A., Arneth, A., Hakola, H., Hayward, S. & Holst, T. (2009) Isoprene emission from wetland sedges. Biogeosciences, 6, 601-613.
Ekberg, A., Arneth, A. & Holst, T. (2011) Isoprene emission from sphagnum species occupying different growth positions above the water table. Boreal Environment Research, 16, 47-59.
El Khawand, M., Crombie, A.T., Johnston, A., Vavlline, D.V., McAuliffe, J.C., Latone, J.A. et al. (2016) Isolation of isoprene degrading bacteria from soils, development of isoA gene probes and identification of the active isoprene-degrading soil community using DNA-stable isotope probing. Environmental Microbiology, 18, 2743-2753.
Ewers, J., Freier-Schrӧder, D. & Knackmuss, H. (1990) Selection of trichloroethene (TCE) degrading bacteria that resist inactivation by TCE. Archives of Microbiology, 154, 410-413.
Exton, D.A., Suggett, D.J., McGenity, T.J. & Steinke, M. (2013) Chlorophyll-normalized isoprene production in laboratory cultures of marine microalgae and implications for global models. Limnology and Oceanography, 58, 1301-1311.
Exton, D.A., Suggett, D.J., Steinke, M. & McGenity, T.J. (2012) Spatial and temporal variability of biogenic isoprene emissions from a temperate estuary. Global Biogeochem Cycles, 26, 1-13.
Gallagher, S.C., Cammack, R. & Dalton, H. (1997) Alkene monooxygenase from Nocardia corallina B-276 is a member of the class of dinuclear iron proteins capable of stereospecific epoxygenation reactions. European Journal of Biochemistry, 247, 635-641.
Gibson, L., Crombie, A.T., McNamara, N.P. & Murrell, J.C. (2021) Isoprene-degrading bacteria associated with the phyllosphere of Salix fragilis, a high isoprene-emitting willow of the northern hemisphere. Environmental Microbiomes, 16, 1-13.
Gibson, L., Larke-Mejía, N.L. & Murrell, J.C. (2020) Complete genome of isoprene degrading Nocardioides sp. WS12. Microorganisms, 8(6), 889. Available from: https://doi.org/10.3390/microorganisms8060889
Gray, C.M., Helmig, D. & Fierer, N. (2015) Bacteria and fungi associated with isoprene consumption in soil. Elementa, 3, 000053. Available from: https://doi.org/10.12952/journal.elementa.000053
Green, J. & Dalton, H. (1986) Steady-state kinetic analysis of soluble methane mono-oxygenase from Methylococcus capsulatus (Bath). The Biochemical Journal, 236, 155-162.
Hellén, H., Schallhart, S., Praplan, A.P., Tykkä, T., Aurela, M., Lohila, A. et al. (2020) Sesquiterpenes dominate monoterpenes in northern wetland emissions. Atmospheric Chemistry and Physics, 20, 7021-7034.
Hrebien, V., Deschaseaux, E., Eickhoff, W., Swan, H.B. & Eyre, B.D. (2020) Quantification of isoprene in coastal ecosystems by gas chromatography-mass spectrometry using cumulative headspace injections. Limnology and Oceanography: Methods, 18, 374-382.
Johnson, T., Newton, G.L., Fahey, R.C. & Rawat, M. (2009) Unusual production of glutathione in Actinobacteria. Archives of Microbiology, 191, 89-93.
Johnston, A., Crombie, A.T., El Khawand, M., Sims, L., Whited, G.M., McGenity, T.J. et al. (2017) Identification and characterisation of isoprene-degrading bacteria in an estuarine environment. Environmental Microbiology, 19, 3526-3537.
Kronen, M. (2019) Anaerobic microbial metabolism of isoprene. PhD Thesis. Australia: University of New South Wales.
Kronen, M., Lee, M., Jones, Z.L. & Manefield, M.J. (2019) Reductive metabolism of the important atmospheric gas isoprene by homoacetogens. The ISME Journal, 13, 1168-1182.
Kuzma, J., Nemecek-Marshall, M., Pollock, W.H. & Fall, R. (1995) Bacteria produce the volatile hydrocarbon isoprene. Current Microbiology, 30, 97-103.
Larke-Mejía, N.L., Carrión, O., Crombie, A.T., McGenity, T.J. & Murrell, J.C. (2020) Sphingopyxis sp. strain OPL5, an isoprene-degrading bacterium from the sphingomonadaceae family isolated from oil palm leaves. Microorganisms, 8(10), 1557. Available from: https://doi.org/10.3390/microorganisms8101557
Larke-Mejía, N.L., Crombie, A.T., Pratscher, J., McGenity, T.J. & Murrell, J.C. (2019) Novel isoprene-degrading proteobacteria from soil and leaves identified by cultivation and metagenomics analysis of stable isotope probing experiments. Frontiers in Microbiology, 10, 2700. Available from: https://doi.org/10.3389/fmicb.2019.02700
Larmola, T., Tuittila, E.-S., Tiirola, M., Nykänen, H., Martikainen, P.J., Yrjälä, K. et al. (2010) The role of Sphagnum mosses in the methane cycling of a boreal mire. Ecology, 91, 2356-2365.
Leahy, J.G., Batchelor, P.J. & Morcomb, S.M. (2003) Evolution of the soluble diiron monooxygenases. FEMS Microbiology Reviews, 27, 449-479.
Lienkamp, A.C., Burnik, J., Heine, T., Hofmann, E. & Tischler, D. (2021) Characterization of the glutathione S-transferases involved in styrene degradation in Gordonia rubripertincta CWB2. Microbiology Spectrum, 9, e00474-e00421.
Luo, G. & Yu, F. (2010) A numerical evaluation of global oceanic emissions of α-pinene and isoprene. Atmospheric Chemistry and Physics, 10, 2007-2015. Available from: https://doi.org/10.5194/acp-10-2007-2010
Miura, A. & Dalton, H. (1995) Purification and characterization of the alkene monooxygenase from Nocardia corallina B-276. Bioscience, Biotechnology, and Biochemistry, 59, 853-859.
Moore, E.R., Davie-Martin, C.L., Giovannoni, S.J. & Halsey, K.H. (2020) Pelagibacter metabolism of diatom-derived volatile organic compounds imposes an energetic tax on photosynthetic carbon fixation. Environmental Microbiology, 22, 1720-1733.
Moore, E.R., Weaver, A.J., Davis, E.W., Giovannoni, S.J. & Halsey, K.H. (2022) Metabolism of key atmospheric volatile organic compounds by the marine heterotrophic bacterium Pelagibacter HTCC1062 (SAR11). Environmental Microbiology, 24, 212-222.
Mooshammer, M., Kitzinger, K., Schintlmeister, A., Ahmerkamp, S., Nielsen, J.L., Nielsen, P.H. et al. (2021) Flow-through stable isotope probing (flow-SIP) minimizes cross-feeding in complex microbial communities. The ISME Journal, 15, 348-353. Available from: https://doi.org/10.1038/s41396-020-00761-5
Morris, R.M., Rappé, M.S., Connon, S.A., Vergin, K.L., Siebold, W.A., Carlson, C.A. et al. (2002) SAR11 clade dominates ocean surface bacterioplankton communities. Nature, 420, 806-810.
Neufeld, J.D., Dumont, M.G., Vohra, J. & Murrell, J.C. (2007) Methodological considerations for the use of stable isotope probing in microbial ecology. Microbial Ecology, 53, 435-442.
Nkongolo, K.K. & Narendrula-Kotha, R. (2020) Advances in monitoring soil microbial community dynamic and function. Journal of Applied Genetics, 61, 249-263.
Onwukwe, G.U., Kursula, P., Koski, M.K., Schmitz, W. & Wierenga, R.K. (2015) Human Δ3,Δ2-enoyl-CoA isomerase, type 2: A structural enzymology study on the catalytic role of its ACBP domain and helix-10. The FEBS Journal, 282, 746-768.
Ooki, A., Nomura, D., Nishino, S., Kikuchi, T. & Yokouchi, Y. (2015) A global-scale map of isoprene and volatile organic iodine in surface seawater of the Arctic, Northwest Pacific, Indian, and southern oceans. Journal of Geophysical Research: Oceans, 120, 4108-4128.
Prior, S.D. & Dalton, H. (1985) Acetylene as a suicide substrate and active site probe for methane monooxygenase from Methylococcus capsulatus (Bath). FEMS Microbiology Letters, 29, 105-109.
Raghoebarsing, A.A., Smolders, A.J.P., Schmid, M.C., Rijpstra, W.I.C., Wolters-Arts, M., Derksen, J. et al. (2005) Methanotrophic symbionts provide carbon for photosynthesis in peat bogs. Nature, 436, 1153-1156.
Sander, R. (2015) Compilation of Henry's law constants (version 4.0) for water as solvent. Atmospheric Chemistry and Physics, 15, 4399-4981.
Seco, R., Holst, T., Matzen, M.S., Westergaard-Nielsen, A., Li, T., Simin, T. et al. (2020) Volatile organic compound fluxes in a subarctic peatland and lake. Atmos Chem Phys Discuss, 20, 1-32.
Sharkey, T.D., Wiberley, A.E. & Donohue, A.R. (2008) Isoprene emission from plants: why and how. Annals of Botany, 101, 5-18.
Sharkey, T.D. & Yeh, S. (2001) Isoprene emission from plants. Annual Review of Plant Physiology and Plant Molecular Biology, 52, 407-436.
Sims, L.P., Lockwood, C.W.J., Crombie, A.T., Bradley, J.M., Le Brun, N.E. & Murrell, J.C. (2022) Purification and characterization of the isoprene monooxygenase from Rhodococcus sp. strain AD45. Applied and Environmental Microbiology, 88, e0002922. Available from: https://doi.org/10.1128/aem.00029-22
Singh, A., Srivastava, N. & Dubey, S.K. (2019) Molecular characterization and kinetics of isoprene degrading bacteria. Bioresource Technology, 278, 51-56.
Spielmann, F.M., Langebner, S., Ghirardo, A., Hansel, A., Schnitzler, J.P. & Wohlfahrt, G. (2017) Isoprene and α-pinene deposition to grassland mesocosms. Plant and Soil, 410, 313-322.
Srivastva, N., Shukla, A.K., Singh, R.S., Upadhyay, S.N. & Dubey, S.K. (2015) Characterization of bacterial isolates from rubber dump site and their use in biodegradation of isoprene in batch and continuous bioreactors. Bioresource Technology, 188, 84-91.
Srivastva, N., Vishwakarma, P., Bhardwaj, Y., Singh, A., Manjunath, K. & Dubey, S.K. (2017) Kinetic and molecular analyses reveal isoprene degradation potential of Methylobacterium sp. Bioresource Technology, 242, 87-91.
Steinke, M., Hodapp, B., Subhan, R., Bell, T.G. & Martin-Creuzburg, D. (2018) Flux of the biogenic volatiles isoprene and dimethyl sulfide from an oligotrophic lake. Scientific Reports, 8, 630. Available from: https://doi.org/10.1038/s41598-017-18923-5
Takagi, M., Uemura, N. & Furuhashi, K. (1990) Microbial transformation processes of aliphatic hydrocarbons. Annals of the New York Academy of Sciences, 613, 697-701.
Textor, S., Wendisch, V.F., De Graaf, A.A., Müller, U., Linder, M.I., Linder, D. et al. (1997) Propionate oxidation in Escherichia coli: evidence for operation of a methylcitrate cycle in bacteria. Archives of Microbiology, 168, 428-436.
Tripathi, N., Sahu, L.K., Singh, A., Yadav, R. & Karati, K.K. (2020) High levels of isoprene in the marine boundary layer of the Arabian Sea during spring inter-monsoon: role of phytoplankton blooms. ACS Earth and Space Chemistry, 4, 583-590.
Uttarotai, T., McKew, B.A., Benyahia, F., Murrell, J.C., Mhuantong, W., Wangkarn, S. et al. (2021) Isoprene-degrading bacteria from soils associated with tropical economic crops and framework forest trees. Microorganisms, 9(5), 1024. Available from: https://doi.org/10.3390/microorganisms9051024
Uttarotai, T., Sutheeworapong, S., Crombie, A.T., Murrell, J.C., Mhuantong, W., Noirungsee, N. et al. (2022) Genome characterisation of an isoprene-degrading Alcaligenes sp. isolated from a tropical restored Forest. Biology (Basel), 11, 519.
van Doorn, M.M., Merl-Pham, J., Ghirardo, A., Fink, S., Polle, A., Schnitzler, J.-P. et al. (2020) Root isoprene formation alters lateral root development. Plant, Cell & Environment, 43, 2207-2223.
van Hylckama Vlieg, J.E.T., Kingma, J., Kruizinga, W. & Janssen, D.B. (1999) Purification of a glutathione S-transferase and a glutathione conjugate-specific dehydrogenase involved in isoprene metabolism in Rhodococcus sp. strain AD45. Journal of Bacteriology, 181, 2094-2101.
van Hylckama Vlieg, J.E.T., Kingma, J., van den Wijngaard, A.J. & Janssen, D.B.D. (1998) A glutathione S-transferase with activity towards cis-1,2-dichloroepoxyethane is involved in isoprene utilization by Rhodococcus sp. strain AD45. Applied and Environmental Microbiology, 64, 2800-2805.
van Hylckama Vlieg, J.E.T., Leemhuis, H., Jeffrey, H., Spelberg, L. & Janssen, D.B. (2000) Characterization of the gene cluster involved in isoprene metabolism in Rhodococcus sp. strain AD45. Journal of Bacteriology, 182, 1956-1963.
Wagner, W.P., Helmig, D. & Fall, R. (2000) Isoprene biosynthesis in Bacillus subtilis via the methylerythritol phosphate pathway. Journal of Natural Products, 63, 37-40.
Watson, W.P., Cottrell, L., Zhang, D. & Golding, B.T. (2001) Metabolism and molecular toxicology of isoprene. Chemico-Biological Interactions, 135-136, 223-238.
Wright, C.L., Schatteman, A., Crombie, A.T., Murrell, J.C. & Lehtovirta-Morley, L.E. (2020) Inhibition of ammonia monooxygenase from ammonia-oxidizing archaea by linear and aromatic alkynes. Applied and Environmental Microbiology, 86, e02388-e02319.
Yeager, C.M., Bottomley, P.J., Arp, D.J. & Hyman, M.R. (1999) Inactivation of toluene 2-monooxygenase in Burkholderia cepacia G4 by alkynes. Applied and Environmental Microbiology, 65, 632-639.
Yu, J., Moon, S.-K., Kim, Y.-H. & Min, J. (2022) Isoprene production by Rhodobacter sphaeroides and its antimicrobial activity. Research in Microbiology, 173, 103938.
Zhao, L., Chang, W.W., Xiao, Y., Liu, H.H. & Liu, P. (2013) Methylerythritol phosphate pathway of isoprenoid biosynthesis. Annual Review of Biochemistry, 82, 497-530.
Zuo, Z. (2019) Why algae release volatile organic compounds-the emission and roles. Frontiers in Microbiology, 10, 491. Available from: https://doi.org/10.3389/fmicb.2019.00491

Auteurs

Robin A Dawson (RA)

School of Environmental Sciences, University of East Anglia, Norwich Research Park, Norwich, UK.

Andrew T Crombie (AT)

School of Environmental Sciences, University of East Anglia, Norwich Research Park, Norwich, UK.

Robert S Jansen (RS)

Department of Microbiology, Radboud University, Nijmegen, The Netherlands.

Thomas J Smith (TJ)

Biomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.

Tim Nichol (T)

Biomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.

Colin Murrell (C)

School of Environmental Sciences, University of East Anglia, Norwich Research Park, Norwich, UK.

Articles similaires

Populus Soil Microbiology Soil Microbiota Fungi
Aerosols Humans Decontamination Air Microbiology Masks
Coal Metagenome Phylogeny Bacteria Genome, Bacterial
Semiconductors Photosynthesis Polymers Carbon Dioxide Bacteria

Classifications MeSH