Large-Scale 13C flux profiling reveals conservation of the Entner-Doudoroff pathway as a glycolytic strategy among marine bacteria that use glucose

Appl Environ Microbiol. 2015 Apr;81(7):2408-22. doi: 10.1128/AEM.03157-14. Epub 2015 Jan 23.

Abstract

Marine bacteria form one of the largest living surfaces on Earth, and their metabolic activity is of fundamental importance for global nutrient cycling. Here, we explored the largely unknown intracellular pathways in 25 microbes representing different classes of marine bacteria that use glucose: Alphaproteobacteria, Gammaproteobacteria, and Flavobacteriia of the Bacteriodetes phylum. We used (13)C isotope experiments to infer metabolic fluxes through their carbon core pathways. Notably, 90% of all strains studied use the Entner-Doudoroff (ED) pathway for glucose catabolism, whereas only 10% rely on the Embden-Meyerhof-Parnas (EMP) pathway. This result differed dramatically from the terrestrial model strains studied, which preferentially used the EMP pathway yielding high levels of ATP. Strains using the ED pathway exhibited a more robust resistance against the oxidative stress typically found in this environment. An important feature contributing to the preferential use of the ED pathway in the oceans could therefore be enhanced supply of NADPH through this pathway. The marine bacteria studied did not specifically rely on a distinct anaplerotic route, but the carboxylation of phosphoenolpyruvate (PEP) or pyruvate for fueling of the tricarboxylic acid (TCA) cycle was evenly distributed. The marine isolates studied belong to clades that dominate the uptake of glucose, a major carbon source for bacteria in seawater. Therefore, the ED pathway may play a significant role in the cycling of mono- and polysaccharides by bacterial communities in marine ecosystems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aquatic Organisms / genetics
  • Aquatic Organisms / metabolism*
  • Bacteria / genetics
  • Bacteria / metabolism*
  • Carbon Isotopes / metabolism*
  • Citric Acid Cycle
  • Glucose / metabolism*
  • Glycolysis*
  • Isotope Labeling*
  • Metabolic Flux Analysis*
  • Molecular Sequence Data
  • Phosphoenolpyruvate / metabolism
  • Pyruvic Acid / metabolism
  • Sequence Analysis, DNA

Substances

  • Carbon Isotopes
  • Phosphoenolpyruvate
  • Pyruvic Acid
  • Glucose

Associated data

  • GENBANK/KC731427
  • GENBANK/KC731428
  • GENBANK/KC754372
  • GENBANK/KC754373
  • GENBANK/KC754374
  • GENBANK/KC754375
  • GENBANK/KC754376
  • GENBANK/KC812726
  • GENBANK/KC812727
  • GENBANK/KC812728