AI Article Synopsis

  • Plants and phytoplankton release volatile organic compounds (VOCs) like acetone and isoprene, which can affect atmospheric chemistry.
  • Research found that the marine bacterium Pelagibacter (strain HTCC1062) can metabolize these VOCs, possibly significantly impacting the overall marine acetone and isoprene budgets when considering global populations.
  • The HTCC1062 genome shows some genes related to acetone metabolism, but lacks the known pathway for isoprene degradation, suggesting an unknown method for isoprene uptake and that it can synthesize isoprenoid compounds when provided with isoprene.

Article Abstract

Plants and phytoplankton are natural sources of the volatile organic compounds (VOCs) acetone and isoprene, which are reactive and can alter atmospheric chemistry. In earlier research we reported that, when co-cultured with a diatom, the marine bacterium Pelagibacter (strain HTCC1062; 'SAR11 clade') reduced the concentration of compounds tentatively identified as acetone and isoprene. In this study, experiments with Pelagibacter monocultures confirmed that these cells are capable of metabolizing acetone and isoprene at rates similar to bacterial communities in seawater and high enough to consume substantial fractions of the total marine acetone and isoprene budgets if extrapolated to global SAR11 populations. Homologues of an acetone/cyclohexanone monooxygenase were identified in the HTCC1062 genome and in the genomes of a wide variety of other abundant marine taxa, and were expressed at substantial levels (c. 10 of transcripts) across TARA oceans metatranscriptomes from ocean surface samples. The HTCC1062 genome lacks the canonical isoprene degradation pathway, suggesting an unknown alternative biochemical pathway is used by these cells for isoprene uptake. Fosmidomycin, an inhibitor of bacterial isoprenoid biosynthesis, blocked HTCC1062 growth, but the cells were rescued when isoprene was added to the culture, indicating SAR11 cells may be capable of synthesizing isoprenoid compounds from exogenous isoprene.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300024PMC
http://dx.doi.org/10.1111/1462-2920.15837DOI Listing

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