4.6 Article

Distribution and expression of microbial rhodopsins in the Baltic Sea and adjacent waters

期刊

ENVIRONMENTAL MICROBIOLOGY
卷 18, 期 12, 页码 4442-4455

出版社

WILEY
DOI: 10.1111/1462-2920.13407

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资金

  1. Baltic-Sea2020 Foundation
  2. Olle Engkvist Byggmastare Foundation
  3. Science for Life Laboratory (Stockholm)
  4. Baltic Sea Adaptive Management (BEAM) program
  5. Goran Gustafsson Foundation for Research in Natural Sciences and Medicine
  6. Swedish Research Council
  7. Science for Life Laboratory
  8. Knut and Alice Wallenberg Foundation
  9. National Genomics Infrastructure - Swedish Research Council
  10. BILS (Bioinformatics Infrastructure for Life Sciences)

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Rhodopsins are light-driven ion-pumping membrane proteins found in many organisms and are proposed to be of global importance for oceanic microbial energy generation. Several studies have focused on marine environments, with less exploration of rhodopsins in brackish waters. We investigated microbial rhodopsins in the Baltic Sea using size-fractionated metagenomic and metatranscriptomic datasets collected along a salinity gradient spanning from similar to 0 to 35 PSU. The normalised genomic abundance of rhodopsins in Bacteria, as well as rhodopsin gene expression, was highest in the smallest size fraction (0.1-0.8 mu m), relative to the medium (0.8-3.0 mu m) and large (> 3.0 mu m) size fractions. The abundance of rhodopsins in the two smaller size fractions displayed a positive correlation with salinity. Proteobacteria and Bacteroidetes rhodopsins were the most abundant while Actinobacteria rhodopsins, or actinorhodopsins, were common at lower salinities. Phylogenetic analysis indicated that rhodopsins have adapted independently to the marine-brackish transition on multiple occasions, giving rise to green light-adapted variants from ancestral blue light-adapted ones. A notable diversity of viral-like rhodopsins was also detected in the dataset and potentially linked with eukaryotic phytoplankton blooms. Finally, a new clade of likely proton-pumping rhodopsin with non-canonical amino acids in the spectral tuning and proton accepting site was identified.

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