Metaproteomics of aquatic microbial communities in a deep and stratified estuary

Proteomics. 2015 Oct;15(20):3566-79. doi: 10.1002/pmic.201500079. Epub 2015 Sep 10.

Abstract

Here we harnessed the power of metaproteomics to assess the metabolic diversity and function of stratified aquatic microbial communities in the deep and expansive Lower St. Lawrence Estuary, located in eastern Canada. Vertical profiling of the microbial communities through the stratified water column revealed differences in metabolic lifestyles and in carbon and nitrogen processing pathways. In productive surface waters, we identified heterotrophic populations involved in the processing of high and low molecular weight organic matter from both terrestrial (e.g. cellulose and xylose) and marine (e.g. organic compatible osmolytes) sources. In the less productive deep waters, chemosynthetic production coupled to nitrification by MG-I Thaumarchaeota and Nitrospina appeared to be a dominant metabolic strategy. Similar to other studies of the coastal ocean, we identified methanol oxidation proteins originating from the common OM43 marine clade. However, we also identified a novel lineage of methanol-oxidizers specifically in the particle-rich bottom (i.e. nepheloid) layer. Membrane transport proteins assigned to the uncultivated MG-II Euryarchaeota were also specifically detected in the nepheloid layer. In total, these results revealed strong vertical structure of microbial taxa and metabolic activities, as well as the presence of specific "nepheloid" taxa that may contribute significantly to coastal ocean nutrient cycling.

Keywords: Carbon cycle; Marine microbiology; Metagenomics; Microbiology; Nitrification; Ocean.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Archaea / genetics*
  • Bacteria / genetics*
  • Canada
  • Carbon / metabolism
  • Membrane Transport Proteins / biosynthesis
  • Membrane Transport Proteins / genetics*
  • Metagenomics
  • Nitrification / genetics
  • Nitrogen / metabolism
  • Proteomics*
  • Water Microbiology

Substances

  • Membrane Transport Proteins
  • Carbon
  • Nitrogen