4.6 Article

Potential Activities and Long Lifetimes of Organic Carbon-Degrading Extracellular Enzymes in Deep Subsurface Sediments of the Baltic Sea

Journal

FRONTIERS IN MICROBIOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.702015

Keywords

extracellular enzymatic activity; Baltic Sea; International Ocean Discovery Program 347; peptidase activities; subsurface microbial ecosystem

Categories

Funding

  1. NSF [OCE1431498]
  2. NSF Center for Dark energy Biosphere Investigations [OCE-0939564, 576]
  3. Department of Energy, Office of Science, Office of Biological and Environmental Research [DE-SC0020369]
  4. U.S. Department of Energy (DOE) [DE-SC0020369] Funding Source: U.S. Department of Energy (DOE)

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Heterotrophic microorganisms in marine sediments produce extracellular enzymes to hydrolyze organic macromolecules, which can be used for energy and growth. Research in the Baltic Sea Basin has measured potential activities of multiple organic carbon-degrading enzymes, revealing their stability and potential for long enzyme lifetimes in subsurface sediments.
Heterotrophic microorganisms in marine sediments produce extracellular enzymes to hydrolyze organic macromolecules, so their products can be transported inside the cell and used for energy and growth. Therefore, extracellular enzymes may mediate the fate of organic carbon in sediments. The Baltic Sea Basin is a primarily depositional environment with high potential for organic matter preservation. The potential activities of multiple organic carbon-degrading enzymes were measured in samples obtained by the International Ocean Discovery Program Expedition 347 from the Little Belt Strait, Denmark, core M0059C. Potential maximum hydrolysis rates (V-max) were measured at depths down to 77.9mbsf for the following enzymes: alkaline phosphatase, beta-d-xylosidase, beta-d-cellobiohydrolase, N-acetyl-beta-d-glucosaminidase, beta-glucosidase, alpha-glucosidase, leucyl aminopeptidase, arginyl aminopeptidase, prolyl aminopeptidase, gingipain, and clostripain. Extracellular peptidase activities were detectable at depths shallower than 54.95mbsf, and alkaline phosphatase activity was detectable throughout the core, albeit against a relatively high activity in autoclaved sediments. beta-glucosidase activities were detected above 30mbsf; however, activities of other glycosyl hydrolases (beta-xylosidase, beta-cellobiohydrolase, N-acetyl-beta-glucosaminidase, and alpha-glucosidase) were generally indistinguishable from zero at all depths. These extracellular enzymes appear to be extremely stable: Among all enzymes, a median of 51.3% of enzyme activity was retained after autoclaving for an hour. We show that enzyme turnover times scale with the inverse of community metabolic rates, such that enzyme lifetimes in subsurface sediments, in which metabolic rates are very slow, are likely to be extraordinarily long. A back-of-the-envelope calculation suggests enzyme lifetimes are, at minimum, on the order of 230days, and may be substantially longer. These results lend empirical support to the hypothesis that a population of subsurface microbes persist by using extracellular enzymes to slowly metabolize old, highly degraded organic carbon.

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