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Mar Drugs
2021 Dec 23;201:. doi: 10.3390/md20010017.
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Investigation of Deep-Sea Ecosystems Using Marker Fatty Acids: Sources of Essential Polyunsaturated Fatty Acids in Abyssal Megafauna.
Svetashev VI
.
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Abyssal seafloor ecosystems cover more than 50% of the Earth's surface. Being formed by mainly heterotrophic organisms, they depend on the flux of particulate organic matter (POM) photosynthetically produced in the surface layer of the ocean. As dead phytoplankton sinks from the euphotic to the abyssal zone, the trophic value of POM and the concentration of essential polyunsaturated fatty acids (PUFA) decrease. This results in pronounced food periodicity and limitations for bottom dwellers. Deep-sea invertebrate seston eaters and surface deposit feeders consume the sinking POM. Other invertebrates utilize different food items that have undergone a trophic upgrade, with PUFA synthesized from saturated and monounsaturated FA. Foraminifera and nematodes can synthesize arachidonic acid (AA), eicosapentaenoic acid (EPA), while some barophylic bacteria produce EPA and/or docosahexaenoic acid. FA analysis of deep-sea invertebrates has shown high levels of PUFA including, in particular, arachidonic acid, bacterial FA, and a vast number of new and uncommon fatty acids such as 21:4(n-7), 22:4(n-8), 23:4(n-9), and 22:5(n-5) characteristic of foraminifera. We suppose that bacteria growing on detritus having a low trophic value provide the first trophic upgrading of organic matter for foraminifera and nematodes. In turn, these metazoans perform the second-stage upgrading for megafauna invertebrates. Deep-sea megafauna, including major members of Echinodermata, Mollusca, and Polychaeta display FA markers characteristic of bacteria, foraminifera, and nematodes and reveal new markers in the food chain.
Figure 1. A part of the GC chromatogram of FAME from TL of the abyssal sea star Eremicaster vicinus. Conditions: Supelcowax 10 column, 30 m, at 205 °C, detector FID. FAME of 21:4(n-7), 22:4(n-8), 22:5(n-5), 23:4(n-9), and 22:6(n-2) acids had ECL values of 22.09, 22.98, 23.53, 23.82, and 24.53, respectively. Uncommon and new acids are underlined.
Baird,
Biomass and community structure of the abyssal microbiota determined from the ester-linked phospholipids recovered from Venezuela Basin and Puerto Rico Trench sediments.
1985, Pubmed
Baird,
Biomass and community structure of the abyssal microbiota determined from the ester-linked phospholipids recovered from Venezuela Basin and Puerto Rico Trench sediments.
1985,
Pubmed
Braeckman,
Temporal dynamics in a shallow coastal benthic food web: Insights from fatty acid biomarkers and their stable isotopes.
2015,
Pubmed
Chang,
Odd-chain polyunsaturated fatty acids in thraustochytrids.
2011,
Pubmed
Dalsgaard,
Fatty acid trophic markers in the pelagic marine environment.
2003,
Pubmed
Delong,
Biochemical function and ecological significance of novel bacterial lipids in deep-sea procaryotes.
1986,
Pubmed
DeLong,
Adaptation of the membrane lipids of a deep-sea bacterium to changes in hydrostatic pressure.
1985,
Pubmed
Drazen,
Lipid, sterols and fatty acid composition of abyssal holothurians and ophiuroids from the North-East Pacific Ocean: food web implications.
2008,
Pubmed
,
Echinobase
Fang,
Phospholipid FA of piezophilic bacteria from the deep sea.
2003,
Pubmed
Fodor,
Effects of Temperature and Dietary Lipids on Phospholipid Fatty Acids and Membrane Fluidity in Steinernema carpocapsae.
1994,
Pubmed
Gems,
Longevity and ageing in parasitic and free-living nematodes.
2000,
Pubmed
Gooday,
Protist diversity and function in the dark ocean - Challenging the paradigms of deep-sea ecology with special emphasis on foraminiferans and naked protists.
2020,
Pubmed
Kabeya,
Genes for de novo biosynthesis of omega-3 polyunsaturated fatty acids are widespread in animals.
2018,
Pubmed
Kharlamenko,
New and Uncommon Fatty Acids in Lipids of Deep-Sea Foraminifera.
2017,
Pubmed
LeKieffre,
Surviving anoxia in marine sediments: The metabolic response of ubiquitous benthic foraminifera (Ammonia tepida).
2017,
Pubmed
Monroig,
Biosynthesis of polyunsaturated fatty acids in marine invertebrates: recent advances in molecular mechanisms.
2013,
Pubmed
Paradis,
Localization of a marine source of odd chain-length fatty acids. I. The amphipod Pontoporeia femorata (Kröyer).
1976,
Pubmed
Rothstein,
Biosynthesis of fatty acids in the free-living nematode, Turbatrix aceti.
1968,
Pubmed
Sinensky,
Homeoviscous adaptation--a homeostatic process that regulates the viscosity of membrane lipids in Escherichia coli.
1974,
Pubmed
Smith,
Abyssal food limitation, ecosystem structure and climate change.
2008,
Pubmed
Svetashev,
Mild method for preparation of 4,4-dimethyloxazoline derivatives of polyunsaturated fatty acids for GC-MS.
2011,
Pubmed
Svetashev,
Fatty Acids of Abyssal Echinodermata, the Sea Star Eremicaster vicinus and the Sea Urchin Kamptosoma abyssale: A New Polyunsaturated Fatty Acid Detected, 22:6(n-2).
2020,
Pubmed
,
Echinobase
Svetashev,
Occurrence of Hexacosapolyenoic Acids 26:7(n-3), 26:6(n-3), 26:6(n-6) and 26:5(n-3) in Deep-Sea Brittle Stars from Near the Kuril Islands.
2015,
Pubmed
,
Echinobase
Svetashev,
Isomerization of octadecapentaenoic acid (18:5n-3) in algal lipid samples under derivatization for GC and GC-MS analysis.
2014,
Pubmed
Tanaka,
Effects of growth temperature on the fatty acid composition of the free-living nematode Caenorhabditis elegans.
1996,
Pubmed
Vasskog,
Characterization and cytotoxicity studies of the rare 21:4 n-7 acid and other polyunsaturated fatty acids from the marine opisthobranch Scaphander lignarius, isolated using bioassay guided fractionation.
2012,
Pubmed
Watts,
Genetic dissection of polyunsaturated fatty acid synthesis in Caenorhabditis elegans.
2002,
Pubmed
Zhou,
Caenorhabditis elegans Delta12-desaturase FAT-2 is a bifunctional desaturase able to desaturate a diverse range of fatty acid substrates at the Delta12 and Delta15 positions.
2011,
Pubmed