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Polysaccharide hydrolysis in the presence of oil and dispersants

Insights into potential degradation pathways of exopolymeric substances (EPS) from oil-degrading bacteria

Bibliographic Data

ID21242025
AuthorsKai Ziervogel (0000-0002-4734-1369, University of New Hampshire), Samantha B Joye (0000-0003-1610-451X, University of Georgia), Sara Kleindienst (0000-0001-8304-9149, 3University of Tuebingen, Tuebingen, DE), Sairah Y Malkin (0000-0002-7523-1589, 4University of Maryland, Cambridge, Maryland, US), Uta Passow (0000-0002-2296-6936, St. John's University), Andrew D Steen (0000-0003-4297-4332, Knoxville College), Carol Arnosti (0000-0002-6074-5341, University of North Carolina at Chapel Hill)
EditorsJody W Deming (School of Oceanography, University of Washington a , US), Christine Michel (0000-0001-6150-4825, Fisheries and Oceans Canada, Freshwater Institute b , CA)
Year2019
Volume7
Publication date2019-01-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueElementa Science of the Anthropocene (JOURNAL)
Journal identifiersISSN: 2325-1026 • E-ISSN: 2325-1026
PublisherUniversity of California Press (PUBLISHER • US)
DOI10.1525/elementa.371
OpenAlexW2964728516
LanguageEN
References cited58

Oceanic oil-degrading bacteria produce copious amounts of exopolymeric substances (EPS) that facilitate their access to oil. The fate of EPS in the water column is in part determined by activities of heterotrophic microbes capable of utilizing EPS compounds as carbon and energy sources. To evaluate the potential of natural microbial communities to degrade EPS produced during oil degradation, we measured potential hydrolysis rates of six structurally distinct polysaccharides in two roller bottle experiments, using water from a natural oil seep in the northern Gulf of Mexico. The suite of polysaccharides used to measure the initial step in carbon degradation is indicative of polymers within microbial EPS. The treatments included (i) unamended surface or deep waters (whole water), and water amended with (ii) a water-accommodated fraction of oil (WAF), (iii) oil dispersant Corexit 9500, and (iv) WAF chemically-enhanced with Corexit (CEWAF). The oil and Corexit treatments were employed to simulate conditions during the Deepwater Horizon oil spill. Polysaccharide hydrolysis rates in the surface-water treatments were lowest in the WAF treatment, despite elevated levels of EPS in the form of transparent exopolymer particles (TEP). In contrast, the three deep-water treatments (WAF, Corexit, CEWAF) showed enhanced hydrolysis rates and TEP levels (WAF) compared to the whole water. We also observed variations in the spectrum of polysaccharide-hydrolyzing enzyme activities among the treatments. These substrate specificities were likely driven by activities of oil-degrading bacteria, shaping the pool of EPS and TEP as well as degradation products of hydrocarbons and Corexit compounds. A model calculation of potential turnover rates of organic carbon within the TEP pool suggests extended residence times of TEP in oil-contaminated waters, making them prone to serve as the sticky matrix for oily aggregates known as marine oil snow

Bacteria · Biodegradation · Biology · Dispersant · Hydrolysis · Microbial biodegradation · Microorganism · Polysaccharide · Produced water · Chemistry · Environmental Science · Microbial bioremediation and biosurfactants · Microplastics and Plastic Pollution · Oil Spill Detection and Mitigation · Environmental Chemistry · Environmental Engineering · Organic Chemistry

  • The ecosystem baseline for particle flux in the Northern Gulf of Mexico

    Open Access•S L C Giering, Beizhan Yan et al.•Elementa Science of the…•2018

  • Rapid microbial respiration of oil from the Deepwater Horizon spill in offshore surface waters of the Gulf of Mexico

    Open Access•Bethanie R Edwards, Christopher M Reddy et al.•Environmental Research Letters•2011

  • Marine snow formation in the aftermath of the Deepwater Horizon oil spill in the Gulf of Mexico

    Open Access•Uta Passow, Kai Ziervogel et al.•Environmental Research Letters•2012

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Highly citedNo

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