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The qualitative composition of carotenoids and their seasonal dynamics in tissues of the bivalve Anadara kagoshimensis (Tokunaga, 1906)

  • Ecological Biochemistry
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Abstract

A total of six carotenoids, viz., β-carotene, pectenol A, pectenolone (trans- and cis-isomers), zeaxanthin, diatoxanthin, and alloxanthin, as well as esters of alloand diatoxanthin, have been detected in total carotenoid extracts from the tissues of the bivalve Anadara kagoshimensis (Tokunaga, 1906) using the methods of thin-layer chromatography, high-performance liquid chromatography, mass spectrometry, UV-VIS spectroscopy, and characteristic reactions for the identification of chemical groups. The major group (over 90% of the total carotenoids) is comprised of alloxanthin, pectenolone, and allo- and diatoxanthin esters. Tissues of A. kagoshimensis are typically characterized by cyclic variations in the level of carotenoids over the period from winter to summer, with the maxima in February and June and the minimum in April. The largest contribution to the seasonal carotenoid dynamics is made by the major group of pigments (R 2 = 0.75–0.99), which depends on the pattern of succession of diatomic microalgae during the annual cycle. The pathways of metabolic transformation of the carotenoids in tissues of this bivalve are discussed.

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References

  1. Borodina, A.V. and Soldatov, A.A., Carotenoids in tissues of the common species of Black Sea mollusks, in Chernomorskiye mollyuski: elementy sravnitel’noi i ekologicheskoi biokhimii (Black Sea Mollusks: Elements of Comparative and Ecological Biochemistry), Sevastopol: Inst. Biol. Yuzhn. Morei, 2014), ch. 3, pp. 87–168.

    Google Scholar 

  2. Borodina, A.V., Maoka, T., and Soldatov, A.A., Composition and content of carotenoids in body of the Black Sea gastropod Rapana venosa (Valenviennes, 1846), J. Evol. Biochem. Physiol., 2013, vol. 49, no. 3, pp. 283–290.

    Article  CAS  Google Scholar 

  3. Bryantseva, Yu.V., Features of the seasonal succession of phytocenoses in Sevastopol Bay in 2004–2006, in Mikrovodorosli Chernogo morya: problemy bioraznoobraziya, sokhraneniya i biotekhnologicheskogo ispol’zovaniya (Microalgae of the Black Sea: the Problems of Biodiversity, Conservation, and Biotechnological Use), Sevastopol: EKOSI–Gidrofizika, 2008), pp. 18–29.

    Google Scholar 

  4. Zolotarev, V.N. and Zolotarev, P.N., Bivalve is a new element in the fauna of the Black Sea, Dokl. Akad. Nauk SSSR, 1987, vol. 297, pp. 501–502.

    Google Scholar 

  5. Kiseleva, M.I., Comparative characteristics of benthic communities off the Caucasus coast, in Mnogoletniye izmeneniya zoobentosa Chernogo morya (Long-term Changes in Zoobenthos of the Black Sea), Kyiv: Naukova Dumka, 1992), pp. 84–99.

    Google Scholar 

  6. Kolyuchkina, G.A. and Ismailov, A.D., Parameters of extrapallial fluid of bivalves as nonspecific biomarkers of short-term environmental pollution, Oceanology (Engl. Transl.), 2007, vol. 47, no. 2, pp. 213–220.

    Google Scholar 

  7. Senicheva, M.I., Species diversity, seasonal and interannual variations of microalgae in the plankton off the Crimea coast, in Mikrovodorosli Chernogo morya: problemy bioraznoobraziya, sokhraneniya i biotekhnologicheskogo ispol’zovaniya (Microalgae of the Black Sea: the Problems of Biodiversity, Conservation, and Biotechnological Use), Sevastopol: EKOSI–Gidrofizika, 2008), pp. 5–18.

    Google Scholar 

  8. Sinegub, I.A., Macroobenthos: 1984–2002, in Severozapadnaya chast’ Chernogo morya: biologiya i ekologiya (The Northwestern Black Sea: Biology and Ecology), Kyiv: Naukova Dumka, 2006), pp. 276–286.

    Google Scholar 

  9. Soldatov, A.A., Gostyukhina, O.L., Borodina, A.V., and Golovina, I.V., Qualitative composition of carotenoids, catalase and superoxide dismutase activities in tissues of the bivalve mollusc Anadara inaequivalvis (Bruguiere, 1789), J. Evol. Biochem. Physiol., 2013, vol. 49, no. 4, pp. 389–398.

    Article  CAS  Google Scholar 

  10. Stelmakh, L.V., Kuftarkova, E.A., and Babich, I.I., Seasonal variation in the growth rate of phytoplankton in coastal waters of the Black Sea (off Sevastopol), Morsk. Ekol. Zh., 2009, vol. 13, no. 1, pp. 67–80.

    Google Scholar 

  11. Kholodov, V.I., Pirkova, A.V., and Ladygina, L.V., Vyrashchivaniye midii i ustrits v Chernom more (Cultivation of Mussels and Oysters in the Black Sea), Sevastopol: EKOSI–Gidrofizika, 2010).

    Google Scholar 

  12. Churilova, T.Ya., Finenko, Z.Z., and Akimov, A.I., Pigments of microalgae, in Mikrovodorosli Chernogo morya: problemy bioraznoobraziya, sokhraneniya i biotekhnologicheskogo ispol’zovaniya (Microalgae of the Black Sea: the Problems of Biodiversity, Conservation, and Biotechnological Use), Sevastopol: EKOSI–Gidrofizika, 2008), pp. 301–320.

    Google Scholar 

  13. Enzell, C.R. and Bach, S., Mass spectrometry of carotenoids, in Carotenoids, Vol. 1b: Spectroscopy, Basel: Birkhäuser Verlag, 1995), pp. 261–320.

    Google Scholar 

  14. Eugster, C.H., Chemical derivatization: microscale tests for the presence of common functional groups in carotenoids, in Carotenoids, Vol. 1a: Isolation and Analysis, Basel: Birkhäuser Verlag, 1995), pp. 71–80.

    Google Scholar 

  15. Gomoiu, M.-T., Scapharca inequivalvis (Bruguiere), a new species in the Black Sea, Cercet ri Marine: Recherches Marines, 1984, no. 17, pp. 131–141.

    Google Scholar 

  16. Goodwin, T.W., The Biochemistry of the Carotenoids, Vol. 2: Animals, London: Chapman and Hall, 1984), 2nd Ed.

    Book  Google Scholar 

  17. Ha, B.S., Kang, D.S., Kim, Y.G., and Kim, K.S., Variation in carotenoid pigment and lipids of the arkshell (Anadara broughtonii) according to the environmental factors of the growing area, J. Korean Soc. Food Nutr., 1989, vol. 18, no. 1, pp. 71–92.

    Google Scholar 

  18. Huber, M., Compendium of Bivalves. A Full-Color Guide to 3,300 of the World’s Marine Bivalves. A Status on Bivalvia after 250 Years of Research, Hackenheim: ConchBooks, 2010).

    Google Scholar 

  19. Krapal, A.-Ml., Popa, O.P., Levrd, A.F., et al., Molecular confirmation on the presence of Anadara kagoshimensis (Tokunaga, 1906) (Mollusca: Bivalvia: Arcidae) in the Black Sea, Trav. Mus. Natl. Hist. Nat. “Grigore Antipa”, 2014, vol. 57, no. 1, pp. 9–12.

    Google Scholar 

  20. Maoka, T. and Akimoto, N., Natural product chemistry in carotenoid, some experimental techniques for structural elucidation and analysis of natural carotenoids, Carotenoid Sci., 2008, vol. 13, pp. 10–17.

    Google Scholar 

  21. Maoka, T., Etoh, T., Borodina, A.V., and Soldatov, A.A., A series of 19 or 19’-hexanoyloxycarotenoids from the sea mussel, Mytilus galloprovincialis, grown in the Black Sea of Ukraine, J. Agric. Food Chem., 2011, vol. 59, pp. 13059–13064.

    Article  CAS  PubMed  Google Scholar 

  22. Maoka, T., Fujiwara, Y., Hashimoto, K., and Akimoto, N., Characterization of epoxy carotenoids by fast atom bombardment collision-induced dissociation MS/MS, Lipids, 2004, vol. 39, no. 2, pp. 179–183.

    CAS  PubMed  Google Scholar 

  23. Maoka, T., Fujiwara, Y., Hashimoto, K., and Akimoto, N., Carotenoids in three species of corbicula clams, Corbicula japonica, Corbicula sandai, and Corbicula sp. (Chinese freshwater Corbicula clam), J. Agric. Food Chem., 2005, vol. 53, pp. 8357–8364.

    CAS  PubMed  Google Scholar 

  24. Maoka, T., Hashimoto, K., Akimoto, N., and Fujiwara, Y., Structures of five new carotenoids from the oyster Crassostrea gigas, J. Nat. Prod., 2001, vol. 64, pp. 578–581.

    Article  CAS  PubMed  Google Scholar 

  25. Maoka, T., Ochi, J., Mori, M., and Sakagami, Y., Identification of carotenoids in the freshwater shellfish Unio douglasiae nipponensis, Anodonta lauta, Cipangopaludina chinensis laeta, and Semisulcospira libertine, J. Oleo Sci., 2012, vol. 61, pp. 69–74.

    CAS  Google Scholar 

  26. Matsuno, T. and Maoka, T., Isolation of a new carotenoid, 3,4,3’-trihydroxy-7’,8’-didehydro-ß-carotene from sea mussels, Bull. Jpn. Soc. Sci. Fish., 1981, vol. 47, no. 3, pp. 377–384.

    CAS  Google Scholar 

  27. Matsuno, T. and Maoka, T., Isolation of Diatoxanthin, Pectenoxanthin, Pectenolone, and a new carotenoid, 3,4,3’-trihydroxy-7’,8’-didehydro-ß-carotene from arkshell and related three species of bivalves, Bull. Jpn. Soc. Sci. Fish., 1981, vol. 47, no. 4, pp. 495–499.

    CAS  Google Scholar 

  28. Revkov, N.K., Boltacheva, N.A., Nikolaenko, T.V., and Kolesnikova, E.A., The soft bottom zoobenthos diversity along the Crimean coastal zone of the Black Sea, Oceanology, 2002, vol. 42, no. 4, pp. 561–571.

    Google Scholar 

  29. High-Quality Mass Spectral Database. http://wwwmassbankjp/indexhtml.

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Correspondence to A. V. Borodina.

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Original Russian Text © A.V. Borodina, A.A. Soldatov, 2016, published in Biologiya Morya.

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Borodina, A.V., Soldatov, A.A. The qualitative composition of carotenoids and their seasonal dynamics in tissues of the bivalve Anadara kagoshimensis (Tokunaga, 1906). Russ J Mar Biol 42, 166–177 (2016). https://doi.org/10.1134/S1063074016020024

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