Diversity of fatty acids in different coral species collected in the coastal sea of Nha Trang, Khanh Hoa
Author affiliations
DOI:
https://doi.org/10.15625/1859-3097/21302Keywords:
Lipid, fatty acids, symbiotic, coral, hydrocoral.Abstract
The total of 15 coral samples belonging to soft coral species Sinularia flexibilis, hard coral Acropora sp., and the hydrocoral Millepora platypylla, were collected in the coastal sea of Nha Trang, Khanh Hoa, Vietnam. In these samples, 39 fatty acids were identified in which Sinularia flexibilis sample identified 26 fatty acids, Acropora sp. identified 27 fatty acids, and Millepora platyphylla has the most diverse fatty acid composition with 35 fatty acids. In the coral samples of S. flexibilis, the difference between the ratio of total saturated fatty acids and the polyunsaturated fatty acids was much smaller than that of the other two species. The n-3/n-6 ratio is the highest among Millepora species, up to 4.45; in S. flexibilis and Acropora, this ratio can be lower than 1. Fatty acids 16:0 and 18:0 are the two main fatty acids in total; the content varies between samples of different species but is quite similar amongst samples of the same species. Fatty acids characterized by symbiotic microalgae 16:2n-7, 18:3n-6, 18:4n-3 Fatty acids 18:3n-6 were absent in S. flexibilis samples, minor content in M. platyphylla samples, and relatively significant in Acropora sp. (from 7.07% to 9.59% total fatty acids). Two fatty acids 16:2n-7 and 18:4n-3 were present in all 3 species, the highest in the sample S. flexibilis. The tetracosapolyenoic fatty acids 24:5n-6 and 24:6n-3 are soft coral marker fatty acids, present in only 5 samples of S. flexibilis with 24:5n-6 content ranging from 2.56% to 5.58% total fatty acids, 24:6n-3 is much lower (0.24% to 0.76%). The two PUFAs with the highest concentration were 20:4n-6 and 22:6n-3. 20:4n-6 was present in the total fatty acids of S. flexibilis with a quite high content (9.76% to 17.12% of the total axb), in contrast, the proportion was very low in five Millepora samples and five Acropora samples. 22:6n-3 was significantly high in the five Millepora samples (12.63% to 25.29% total fatty acids) and minor in the samples of the other two species.
Downloads
Metrics
References
Yamashiro, H., Oku, H., Higa, H., Chinen, I., and Sakai, K., 1999. Composition of lipids, fatty acids and sterols in Okinawan corals. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 122(4), 397–407.
Sargent, J., 1995. Origins and functions of egg lipids: nutritional implications. In: Bromage, N. R., and Roberts, R., (eds.). Broodstocks Management and Egg and Larval Quality, pp. 353–372.
Sargent, J. R., Bell, M. V., Bell, J. G., Henderson, R. J., and Tocher, D. R., 1995. Origins and functions of n-3 polyunsaturated fatty acids in marine organisms. Proceedings of the 6th International Colloquium: Phospholipids: characterization, metabolism, and novel biological applications, pp. 248–259.
Pazos, A. J., Román, G., Acosta, C. P., Sánchez, J. L., and Abad, M., 1997. Lipid classes and fatty acid composition in the female gonad of Pecten maximus in relation to reproductive cycle and environmental variables. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 117(3), 393–402.
Imbs, A. B., 2013. Fatty acids and other lipids of corals: composition, distribution, and biosynthesis. Russian Journal of Marine Biology, 39, 153–168.
Ackman, R. G., 1989.Marine biogenic lipids, fats and oils. CRC press, Vol. 2.
Christie, W. W., 2003. Isolation, separation, identification and structural analysis of lipids. Lipid analysis, 3.
Hagen, W., and Auel, H., 2001. Seasonal adaptations and the role of lipids in oceanic zooplankton. Zoology, 104(3-4), 313–326.
Dalsgaard, J., John, M. S., Kattner, G., Müller-Navarra, D., and Hagen, W., 2003. Fatty acid trophic markers in the pelagic marine environment. Advances in marine biology, 46, 225–340.
Ermolenko, E. V., and Sikorskaya, T. V., 2021. Lipidome of the reef-building coral Acropora cerealis: Changes under thermal stress. Biochemical Systematics and Ecology, 97, 104276.
Folch, J., Lees, M., and Stanley, G. S., 1957. A simple method for the isolation and purification of total lipides from animal tissues. Journal of biological chemistry, 226(1), 497–509.
Christie, W. W., 2020. Mass spectrometry of 4,4-dimethyloxazoline (DMOX) derivatives of fatty acids. https://www.lipid-home.co.uk/ms/dmox.html; accessed January 23, 2024.
Christie W. W., 2020. Mass spectrometry of methyl ester derivatives of fatty acids. http://www.lipidhome.co.uk; assessed January 23, 2024.
Imbs, A. B., and Dang, L. T., 2021. Seasonal dynamics of fatty acid biomarkers in the soft coral Sinularia flexibilis, a common species of Indo-Pacific coral reefs. Biochemical Systematics and Ecology, 96, 104246.
Imbs, A. B., Ermolenko, E. V., Grigorchuk, V. P., and Dang, L. T., 2021. Seasonal variation in the lipidome of two species of Millepora hydrocorals from Vietnam coastal waters (the South China Sea). Coral Reefs, 40, 719–734.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Vietnam Academy of Science and Technology
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.