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Endogenic loliolide, phenylethylamine and exogeniccompounds in marine algae

Yıl 2015, Cilt: 21 Sayı: 2, 200 - 207, 20.09.2015

Öz

AbstractEndogenic compound loliolide in marine algae Laurencia obtusa var. pyramidata, Chondria capillaris, Ceramium rubrum, Cystaseira barbata, Ulva rigida, and Ulva intestinalis and phenylethylamine in Chondria capillaris were found. Exogenic compounds were mainly petroleum components and phthalate derivatives. These findings are reported for
the first time for the examined algae. These algae are eaten in some eastern Asian countries but its human consumption is not recommended because they potentially absorb many pollutants from the aquatic environment.

Kaynakça

  • Ali, M.S., Pervez, M.K., Saleem, M., Ahmed, F. (2003) Dichotenone-A and –B: two enones from the marine brown alga Dictyota dichotoma (Hudson) Lamour. Nat. Prod. Res. 17: 301-306.
  • Attaurrahman, S.Z., Choudhary, M.I., Abbas, S.A., Shameel, M. (1991)
  • Stockerine - a novel linear metabolite from Stockeyia indica. Fitoterapia 62: 77- Crotti, A.E.M., Fonseca, T., Hong, H., Staunton, J., Galembeck, S.E., Lopes, N., Gates, P.J. (2004) The fragmentation mechanism of five-membered lactones by electrospray ionisation tandem mass spectrometry. Int. J. Mass Spect. 232: 271- 2
  • Duan, H., Takaishi, Y., Momota, H., Ohmoto, Y., Taki, T. (2002)
  • Immunosuppressive constituents from Saussurea medusa. Phytochem. 59: 85- El Hattab, M., Culioli, G., Valls, R., Richou, M., Piovetti, L. (2008) Apo- fucoxanthinoids and loliolide from the brown alga Cladostephus spongiosus f. verticillatus (Heterokonta, Sphacelariales). Biochem. Syst. Ecol. 36: 447-451.
  • George, M. (1961) Oil pollution in marine organisms. Nature 192:1209.
  • Guven, K.C., Nesimigil, F., Cumalı, S. (2009) Oil pollution in the Black Sea marine organisms during 2003-2006: mussel, shellfish and algae. J. Black
  • Sea/Mediterranean Environ. 15: 165-178. Hiraga, Y., Taino, K., Kurokawa, M., Takagi, R., Ohkata, K. (1997) (-)-Loliolide and other germination inhibitory active constituents in Equisetum arvense. Nat. Prod. Letters 10: 181-186.
  • Ishiwatari, S., Ono, T. (2008) Melanogenesis inhibitor. Jpn. Kokai Tokkyo
  • Koho. (Accessed in May 2015, http://www.j-tokkyo.com/2008/A61K/JP2008- 0566shtml). (In Japanese).
  • Kato, T., Imai, T., Kashimura, K., Saito, N., Masaya, K. (2003) Germination response in wheat grains to dihydroactinidiolide, a germination inhibitor in wheat husks, and related compounds. J. Agric. Food Chem. 51: 2161-2167.
  • Khan, A.M., Noreen, S., Imran, Z.P., Rahman, A., Choudhary, M.I. (2011) A new compound, jolynamine, from marine brown alga Jolyna laminarioides. Nat. Prod. Res. 25: 898.
  • Kimura, J., Maki, N. (2002) New loliolide derivatives from the brown alga
  • Undaria pinnatifida. J. Nat. Prod. 6: 57-58. Klock, F., Baas, M., Cox, H.C., DeLeeaw, F.W., Scheuk, P.A. (1984) Loliolides and dihydroactinidiolide in recent marine sediment probably indicate a major transformation pathway of carotenoids. Tet. Lett. 25: 5577-5580.
  • Kuniyoshi, M. (1985) Germination inhibitors from the brown alga Sargassum crassifolium (Phacophyta, Sargassaceae). Bot. Mar. 28: 501-503.
  • Liu, S.Q., Pezzuto, J.M., Kinghorn, A.D. (1988) Additional biologically active constituents of the Chinese tallow tree (Sapium sebiferum). J. Nat. Prod. 51: 619-6
  • Lu, H., Xie, H., Gong, Y., Wang, Q., Yang, Y. (2011) Secondary metabolites from the seaweed Gracilaria lemaneiformis and their allelopathic effects on
  • Skeletonema costatum. Biochem. Syst. Ecol. 39: 397-400. Okada, N., Shirata, K., Niwano, M., Koshino, H., Uramoto, M. (1994)
  • Immunosuppressive activity of a monoterpene from Eucommia ulmoides. Phytochem. 37: 281-282. Okunade, L., Wiemer, D.F. (1985) (-)-Loliolide, an ant-repellent compound from Xanthoxyllum setulosum. J. Nat. Prod. 48: 472-473.
  • Parameswaran, P.S., Naik, C.G., Das, B., Kamat, S.Y., Bose, A.K., Nair, M.S.R. (1996) Constituents of the brown alga Padina tetrastromatica (Hauck)-II. Ind. J. Chem. Sec. B. 35B: 463-467.
  • Park, K.E., Kim, Y.A., Jung, H.A. Lee, H.J. Ahn, J.W., Lee, B.J., Seo, Y. (2004)
  • Three norisoprenoids from the brown alga Sargassum thunbergii. J. Korean Chem. Soc. 48: 394-400. Percot, A., Yalcin, A., Aysel, V., Erdugan, H., Dural, B., Guven, K.C. (2009a)
  • Alkaloids in marine algae. Nat. Prod. Res. 23: 460-465. Percot, A., Yalcin, A., Aysel, V., Erdugan, H., Durel, B., Guven, K.C. (2009b)
  • Phenylethylamine content in marine alga around Turkish coast. Bot. Mar. 52: 87- Qin, M., Li, X., Yin, S., Wang, C., Wang, B. (2007) Chemical constituents from
  • Sargassum thunbergii. Haiyang Kexue (Marine Sciences) 31: 47-50. Ragasa, C Y., DeLuna, R.D., Hofilena, J.G. (2005) Antimicrobial terpenoids from Pterocarpus indicus. Nat. Prod. Res. 19: 305-309.
  • Rao, B.CH., Pullaiah, K.CH. (1980) Chemical examination of marine algae off
  • Visakhapatnam Coast: Part II – Constituents of Padina tetrastromatica Hauck. Ind. J. Chem. 21B: 605-606. Rasher, D.B., Stout, E.P., Engel, S., Kubanek, J., Hay, M.E. (2011) Macroalgal terpenes function as allelopathic agents against reef corals. Proc. Nat. Acad. Sci. 108: 17726-17731.
  • Ravi, B.N. Murphy, P.T. Lidgard, R.O. Warren, R.G., Wells, R.J. (1982) C18 terpenoid metabolites of the brown alga Cystophora moniliformis. Aust. J. Chem. 35: 171-182.
  • Rocha, O.P., DeFelicio, R., Rodrigues, A.H.B., Ambrosio, D.L., Cicarelli, R.M.B., DeAlbuquerque, S., Young, M.C.M., Yokoya, N.S., Debonsi, H.M. (2011) Chemical profile and biological potential of non-polar fractions from
  • Centroceras clavulatum (C. Agardh) Montagne (Ceramiales, Rhodophyta). Molecules 16: 7105-7114.
  • Sabelli, H., Fink, P., Fawceit, F., Tom, C. (1996) Sustained effect of PEA replacement. J. Neuropsyc 8: 168-171.
  • Shah, Z. (1990) Studies on the Chemical Constituents of Stokeyia indica,
  • Ervatamia coronaria and Caplophyllum Species. PhD Thesis, H.E.J Research Institute of Chemistry, University of Karachi. Shaikh, W. (1993) Taxanomic and Phycochemical Studies of Certain Brown
  • Algae from the Coast of Karachi. PhD Thesis, Department of Botany, University of Karachi. Shi, D.Y., Han, L.J., Sun, J., Yang, Y.C., Shi, J.G., Fun, X. (2005) Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity. Zhongguo Zhongyao Zazhi 30: 1162-1165.
  • Smith, T.A. (1977) Phenylethylamine and related compounds in plants. Phytochem. 16: 9-18.
  • Steiner, M., Hartmann, T. (1968) The occurrence and distribution of volatile amines in marine algae. Planta 79: 113–121.
  • Takemoto, T., Takeshita, Y. (1970) Studies on the constituents of Undaria pinnatifida. I: methanol soluble constituents. J. Pharm. Soc. Japan 90: 1057- 10
  • Xian, Q., Chen, H., Liu, H., Zou, H., Yin, D. (2006) Isolation and identification of antialgal compounds from the leaves of Vallisneria spiralis L. by activity- guided fractionation. Environ. Sci. Pollut. Res. 13: 233-237.
  • Yang, X., Kang, M.C., Lee, K.W., Kang, S.M., Leo, W.W., Jean, Y.J. (2011)
  • Antioxidant activity and cell protective effect of loliolide isolated from Sargassum ringgoldianum Subsp. coreanum. Algae 26: 201-208. Yuan, Z.H., Han, L.J., Fan, X., Li, S., Shi, D.Y., Sun, J., Ma, M., Yang, Y.C., Shi, J.G. (2006) Chemical constituents from red alga Corallina pilulifera.
  • Zhongguo Zhongyao Zazhi 31: 1787-1790.
Yıl 2015, Cilt: 21 Sayı: 2, 200 - 207, 20.09.2015

Öz

Kaynakça

  • Ali, M.S., Pervez, M.K., Saleem, M., Ahmed, F. (2003) Dichotenone-A and –B: two enones from the marine brown alga Dictyota dichotoma (Hudson) Lamour. Nat. Prod. Res. 17: 301-306.
  • Attaurrahman, S.Z., Choudhary, M.I., Abbas, S.A., Shameel, M. (1991)
  • Stockerine - a novel linear metabolite from Stockeyia indica. Fitoterapia 62: 77- Crotti, A.E.M., Fonseca, T., Hong, H., Staunton, J., Galembeck, S.E., Lopes, N., Gates, P.J. (2004) The fragmentation mechanism of five-membered lactones by electrospray ionisation tandem mass spectrometry. Int. J. Mass Spect. 232: 271- 2
  • Duan, H., Takaishi, Y., Momota, H., Ohmoto, Y., Taki, T. (2002)
  • Immunosuppressive constituents from Saussurea medusa. Phytochem. 59: 85- El Hattab, M., Culioli, G., Valls, R., Richou, M., Piovetti, L. (2008) Apo- fucoxanthinoids and loliolide from the brown alga Cladostephus spongiosus f. verticillatus (Heterokonta, Sphacelariales). Biochem. Syst. Ecol. 36: 447-451.
  • George, M. (1961) Oil pollution in marine organisms. Nature 192:1209.
  • Guven, K.C., Nesimigil, F., Cumalı, S. (2009) Oil pollution in the Black Sea marine organisms during 2003-2006: mussel, shellfish and algae. J. Black
  • Sea/Mediterranean Environ. 15: 165-178. Hiraga, Y., Taino, K., Kurokawa, M., Takagi, R., Ohkata, K. (1997) (-)-Loliolide and other germination inhibitory active constituents in Equisetum arvense. Nat. Prod. Letters 10: 181-186.
  • Ishiwatari, S., Ono, T. (2008) Melanogenesis inhibitor. Jpn. Kokai Tokkyo
  • Koho. (Accessed in May 2015, http://www.j-tokkyo.com/2008/A61K/JP2008- 0566shtml). (In Japanese).
  • Kato, T., Imai, T., Kashimura, K., Saito, N., Masaya, K. (2003) Germination response in wheat grains to dihydroactinidiolide, a germination inhibitor in wheat husks, and related compounds. J. Agric. Food Chem. 51: 2161-2167.
  • Khan, A.M., Noreen, S., Imran, Z.P., Rahman, A., Choudhary, M.I. (2011) A new compound, jolynamine, from marine brown alga Jolyna laminarioides. Nat. Prod. Res. 25: 898.
  • Kimura, J., Maki, N. (2002) New loliolide derivatives from the brown alga
  • Undaria pinnatifida. J. Nat. Prod. 6: 57-58. Klock, F., Baas, M., Cox, H.C., DeLeeaw, F.W., Scheuk, P.A. (1984) Loliolides and dihydroactinidiolide in recent marine sediment probably indicate a major transformation pathway of carotenoids. Tet. Lett. 25: 5577-5580.
  • Kuniyoshi, M. (1985) Germination inhibitors from the brown alga Sargassum crassifolium (Phacophyta, Sargassaceae). Bot. Mar. 28: 501-503.
  • Liu, S.Q., Pezzuto, J.M., Kinghorn, A.D. (1988) Additional biologically active constituents of the Chinese tallow tree (Sapium sebiferum). J. Nat. Prod. 51: 619-6
  • Lu, H., Xie, H., Gong, Y., Wang, Q., Yang, Y. (2011) Secondary metabolites from the seaweed Gracilaria lemaneiformis and their allelopathic effects on
  • Skeletonema costatum. Biochem. Syst. Ecol. 39: 397-400. Okada, N., Shirata, K., Niwano, M., Koshino, H., Uramoto, M. (1994)
  • Immunosuppressive activity of a monoterpene from Eucommia ulmoides. Phytochem. 37: 281-282. Okunade, L., Wiemer, D.F. (1985) (-)-Loliolide, an ant-repellent compound from Xanthoxyllum setulosum. J. Nat. Prod. 48: 472-473.
  • Parameswaran, P.S., Naik, C.G., Das, B., Kamat, S.Y., Bose, A.K., Nair, M.S.R. (1996) Constituents of the brown alga Padina tetrastromatica (Hauck)-II. Ind. J. Chem. Sec. B. 35B: 463-467.
  • Park, K.E., Kim, Y.A., Jung, H.A. Lee, H.J. Ahn, J.W., Lee, B.J., Seo, Y. (2004)
  • Three norisoprenoids from the brown alga Sargassum thunbergii. J. Korean Chem. Soc. 48: 394-400. Percot, A., Yalcin, A., Aysel, V., Erdugan, H., Dural, B., Guven, K.C. (2009a)
  • Alkaloids in marine algae. Nat. Prod. Res. 23: 460-465. Percot, A., Yalcin, A., Aysel, V., Erdugan, H., Durel, B., Guven, K.C. (2009b)
  • Phenylethylamine content in marine alga around Turkish coast. Bot. Mar. 52: 87- Qin, M., Li, X., Yin, S., Wang, C., Wang, B. (2007) Chemical constituents from
  • Sargassum thunbergii. Haiyang Kexue (Marine Sciences) 31: 47-50. Ragasa, C Y., DeLuna, R.D., Hofilena, J.G. (2005) Antimicrobial terpenoids from Pterocarpus indicus. Nat. Prod. Res. 19: 305-309.
  • Rao, B.CH., Pullaiah, K.CH. (1980) Chemical examination of marine algae off
  • Visakhapatnam Coast: Part II – Constituents of Padina tetrastromatica Hauck. Ind. J. Chem. 21B: 605-606. Rasher, D.B., Stout, E.P., Engel, S., Kubanek, J., Hay, M.E. (2011) Macroalgal terpenes function as allelopathic agents against reef corals. Proc. Nat. Acad. Sci. 108: 17726-17731.
  • Ravi, B.N. Murphy, P.T. Lidgard, R.O. Warren, R.G., Wells, R.J. (1982) C18 terpenoid metabolites of the brown alga Cystophora moniliformis. Aust. J. Chem. 35: 171-182.
  • Rocha, O.P., DeFelicio, R., Rodrigues, A.H.B., Ambrosio, D.L., Cicarelli, R.M.B., DeAlbuquerque, S., Young, M.C.M., Yokoya, N.S., Debonsi, H.M. (2011) Chemical profile and biological potential of non-polar fractions from
  • Centroceras clavulatum (C. Agardh) Montagne (Ceramiales, Rhodophyta). Molecules 16: 7105-7114.
  • Sabelli, H., Fink, P., Fawceit, F., Tom, C. (1996) Sustained effect of PEA replacement. J. Neuropsyc 8: 168-171.
  • Shah, Z. (1990) Studies on the Chemical Constituents of Stokeyia indica,
  • Ervatamia coronaria and Caplophyllum Species. PhD Thesis, H.E.J Research Institute of Chemistry, University of Karachi. Shaikh, W. (1993) Taxanomic and Phycochemical Studies of Certain Brown
  • Algae from the Coast of Karachi. PhD Thesis, Department of Botany, University of Karachi. Shi, D.Y., Han, L.J., Sun, J., Yang, Y.C., Shi, J.G., Fun, X. (2005) Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity. Zhongguo Zhongyao Zazhi 30: 1162-1165.
  • Smith, T.A. (1977) Phenylethylamine and related compounds in plants. Phytochem. 16: 9-18.
  • Steiner, M., Hartmann, T. (1968) The occurrence and distribution of volatile amines in marine algae. Planta 79: 113–121.
  • Takemoto, T., Takeshita, Y. (1970) Studies on the constituents of Undaria pinnatifida. I: methanol soluble constituents. J. Pharm. Soc. Japan 90: 1057- 10
  • Xian, Q., Chen, H., Liu, H., Zou, H., Yin, D. (2006) Isolation and identification of antialgal compounds from the leaves of Vallisneria spiralis L. by activity- guided fractionation. Environ. Sci. Pollut. Res. 13: 233-237.
  • Yang, X., Kang, M.C., Lee, K.W., Kang, S.M., Leo, W.W., Jean, Y.J. (2011)
  • Antioxidant activity and cell protective effect of loliolide isolated from Sargassum ringgoldianum Subsp. coreanum. Algae 26: 201-208. Yuan, Z.H., Han, L.J., Fan, X., Li, S., Shi, D.Y., Sun, J., Ma, M., Yang, Y.C., Shi, J.G. (2006) Chemical constituents from red alga Corallina pilulifera.
  • Zhongguo Zhongyao Zazhi 31: 1787-1790.
Toplam 41 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Articles
Yazarlar

Kasım Cemal Güven Bu kişi benim

Burak Coban Bu kişi benim

Sumru Özkırımlı Bu kişi benim

Huseyin Erdugan Bu kişi benim

Ekrem Sezik Bu kişi benim

Yayımlanma Tarihi 20 Eylül 2015
Yayımlandığı Sayı Yıl 2015 Cilt: 21 Sayı: 2

Kaynak Göster

APA Güven, K. C. ., Coban, B. ., Özkırımlı, S. ., Erdugan, H. ., vd. (2015). Endogenic loliolide, phenylethylamine and exogeniccompounds in marine algae. Journal of Black Sea / Mediterranean Environment, 21(2), 200-207.
AMA Güven KC, Coban B, Özkırımlı S, Erdugan H, Sezik E. Endogenic loliolide, phenylethylamine and exogeniccompounds in marine algae. Journal of Black Sea / Mediterranean Environment. Ağustos 2015;21(2):200-207.
Chicago Güven, Kasım Cemal, Burak Coban, Sumru Özkırımlı, Huseyin Erdugan, ve Ekrem Sezik. “Endogenic Loliolide, Phenylethylamine and Exogeniccompounds in Marine Algae”. Journal of Black Sea / Mediterranean Environment 21, sy. 2 (Ağustos 2015): 200-207.
EndNote Güven KC, Coban B, Özkırımlı S, Erdugan H, Sezik E (01 Ağustos 2015) Endogenic loliolide, phenylethylamine and exogeniccompounds in marine algae. Journal of Black Sea / Mediterranean Environment 21 2 200–207.
IEEE K. C. . Güven, B. . Coban, S. . Özkırımlı, H. . Erdugan, ve E. . Sezik, “Endogenic loliolide, phenylethylamine and exogeniccompounds in marine algae”, Journal of Black Sea / Mediterranean Environment, c. 21, sy. 2, ss. 200–207, 2015.
ISNAD Güven, Kasım Cemal vd. “Endogenic Loliolide, Phenylethylamine and Exogeniccompounds in Marine Algae”. Journal of Black Sea / Mediterranean Environment 21/2 (Ağustos 2015), 200-207.
JAMA Güven KC, Coban B, Özkırımlı S, Erdugan H, Sezik E. Endogenic loliolide, phenylethylamine and exogeniccompounds in marine algae. Journal of Black Sea / Mediterranean Environment. 2015;21:200–207.
MLA Güven, Kasım Cemal vd. “Endogenic Loliolide, Phenylethylamine and Exogeniccompounds in Marine Algae”. Journal of Black Sea / Mediterranean Environment, c. 21, sy. 2, 2015, ss. 200-7.
Vancouver Güven KC, Coban B, Özkırımlı S, Erdugan H, Sezik E. Endogenic loliolide, phenylethylamine and exogeniccompounds in marine algae. Journal of Black Sea / Mediterranean Environment. 2015;21(2):200-7.