4.6 Article

Metabolism of key atmospheric volatile organic compounds by the marine heterotrophic bacterium Pelagibacter HTCC1062 (SAR11)

Journal

ENVIRONMENTAL MICROBIOLOGY
Volume 24, Issue 1, Pages 212-222

Publisher

WILEY
DOI: 10.1111/1462-2920.15837

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Funding

  1. NASA North Atlantic Aerosols and Marine Ecosystems Study (NAAMES) [NNX15AE70G]
  2. Simons Foundation International BIOS-SCOPE initiative
  3. NASA [803532, NNX15AE70G] Funding Source: Federal RePORTER

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It was found that the marine bacterium Pelagibacter (SAR11 clade) is capable of reducing the concentration of acetone and isoprene, with the potential to impact the global budgets of these compounds. The cells of Pelagibacter may have the ability to metabolize acetone and isoprene at rates similar to bacterial communities in seawater. Additionally, the genome of Pelagibacter lacks the traditional isoprene degradation pathway, hinting at an alternative biochemical pathway for isoprene uptake.
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(-4) 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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