Mycobiology

  • 제35권2호
  • /
  • Pages.72-75
  • /
  • 2007
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  • 1229-8093(pISSN)
  • /
  • 2092-9323(eISSN)
한국균학회 (The Korean Society of Mycology)
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Antifungal Activity of 2-Hydroxy 4,4'6'Trimethoxy Chalcone

  • Mishra, P.K. (Department of Mycology and Plant Pathology, Institute of Agricultural Sciences, Banaras Hindu University) ;
  • Sarma, B.K. (Department of Mycology and Plant Pathology, Institute of Agricultural Sciences, Banaras Hindu University) ;
  • Singhai, P.K. (Department of Mycology and Plant Pathology, Institute of Agricultural Sciences, Banaras Hindu University) ;
  • Singh, U.P. (Department of Mycology and Plant Pathology, Institute of Agricultural Sciences, Banaras Hindu University)
  • 발행 : 2007.06.30
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초록

Antifungal activity of 2-hydroxy 4,4'6'trimethoxy chalcone individually was tested against spore germination of ten fungi of different genera. Efficacy of the chemical was also tested against conidial germination and other growth parameters of Erysiphe pisi on excised pea leaves. 2-Hydroxy 4,4'6'trimethoxy chalcone inhibited spore germination at all the concentrations. Maximum inhibition was observed at 2000 ppm where more than 78 per cent inhibition of spore germination was observed in Ustilago cynodontis, Alternaria brassicicola, A. solani and Aspergillus flavus. It also reduced conidial germination of E. pisi significantly, when applied as pre-inoculation treatment.

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참고문헌

  1. Attar-ur-Rahman, Nasreen, A., Akhtar, F., Shekhani, M. S., Clardy, J., Parvez, M. and Choudhauri, M. I. 1977. Antifungal diterpenoid alkaoids from Delphinium denudatum. J. Nat. Prod. 60: 474-77
  2. Baptista, M. J. and Siqueira, J. O. 1994. Effect of Flevonoids on spore germination, and asymbiotic growth of the arbuscular mycorrhizal fungus, Gigaspora giganta. Revista brasilaria de Fisiologia vegetal, 6(2), 127-134 [Pt en. 27 ref.] Departmento de Ciencia desolo Escola Superior de Agriculture de Lauras, CP 37, Larras MG 37200-000 Brazil
  3. Carver, T. L. W. and Adaigbe, M. E. 1990. Effects of out host genotype, leaf age and position and incubation humidity on germination and germling developing by Erysiphe graminis f. sp. avenae. Mycol. Res. 94: 18-26 https://doi.org/10.1016/S0953-7562(09)81259-8
  4. Dixon, R. A., Harrison, M. J. and Paiva, N. L. 1995. The isolflavonoid phytoalexin pathway: From enzymeto genes to transcript factor. Physiol. Planta. 93: 385-392 https://doi.org/10.1111/j.1399-3054.1995.tb02243.x
  5. Harborne, J. B. and Grayer, R. J. 1992. Flavonoid and insects. In Horborn, J. B. ed. The Flavonoids: Advances in Research since 1986. London: Chapman and Halls, Pp 589-618
  6. Lyon, G. D., Beglinski, T. and Newton, A. C. 1995. Novel disease control compounds: the potential to 'immunize' plants against infection. Plant Pathol. 44: 407-427 https://doi.org/10.1111/j.1365-3059.1995.tb01664.x
  7. Maillard, M., Gupta, M. P. and Hostelmann, K. 1987. A new antifungal prenylated flavonone from Erythrina berteroana. Planta Med. 53: 563-564 https://doi.org/10.1055/s-2006-962812
  8. Maurya, R. 1984. Chemistry of Natural Products, Ph.D. thesis, of Banaras Hindu University, Varanasi-221 005, India
  9. Maurya, S., Srivastava, J. S., Jha, R. N., Pandey, V. B. and Singh, U. P. 2002. Effect of tetrahydropalmatine, an alkaloid on spore germination of some fungi. Mycobiology 29: 142-144
  10. O'Neil, T. M. and Mansfield, J. W. 1982. Antifungal activity of hydroxyflavans and other flavonoids. Trans. Brit. Mycol. Soc. 79: 229-237 https://doi.org/10.1016/S0007-1536(82)80108-3
  11. Prithiviraj, B., Manickam, M., Singh, U. P. and Ray, A. B. 1997. Antifungal activity of anacardic acid, a naturally occu rring derivative of salicylic a cid. Can. J. Bot. 75: 207-211 https://doi.org/10.1139/b97-021
  12. Prithiviraj, B. and Singh, U. P. 1996. Biological control of plant pathogens: A Key to a serene agroecosystem. J. Rec. Adv. Appl. Sci. 10: 99-110
  13. Prithiviraj, B., Singh, U. P., Singh, K. P. and Plank-Schumacher, K. 1998. Field evaluation of ajoene, as constituent of garlic (Allium sativum) and neemazal, a product of neem (Azadirachta indica) for the control of powdery mildew (Erysiphe p isi) of pea (Pisum sativum). J. Plant Dis. Prot. 105: 274-278
  14. Pueppke, S. G. and Van Etten, H. D. 1976. Accumulation of Pisastin and three additional antifungal Pterocarpans in Fusarium solani infected tissue of Pisum sativum. Physiol. Plant Pathol. 8: 51-61 https://doi.org/10.1016/0048-4059(76)90007-2
  15. Reimers, F., Smolka, S. E., Werres, S., Plank-Schumacher, K. and Wagner, K. G. 1993. Effect of ajoene, a compound derived from Allium sativum, on phytopathogenic and epiphytic micro-organisms. J. Plant Dis. Prot. 100: 622-633
  16. Sarma, B. K., Pandey, V. B., Mishra, G. D. and Singh, U. P. 1999. Antifungal activity of berberine iodide, a constituent of Fumaria indica. Folia Microbiol. 44: 164-166 https://doi.org/10.1007/BF02816235
  17. Singh, U. P., Prithiviraj, B., Wagner, K. G. and Plank-Schumacher, K. 1995. Effect of ajoene, a constituent of garlic (Allium sativum), on powdery mildew (Erysiphe pisi) of pea (Pisum sativum). J. Plant Dis. Prot. 102: 399-406
  18. Singh, U. P., Sarma, B. K., Mishra, P. K. and Ray, A. B. 2000. Antifungal activity of venenatine, an indole alkaloid isolated from Alstonia venenata. Folia Microbiol. 45: 173-176 https://doi.org/10.1007/BF02817419
  19. Siqueira, J. O., Safir, G. R. and Nair, M. G. 1991. Stimulation of VA miccorhiza formation and growth of white clover by flavonoid compounds. New Phytol. 118: 87-93 https://doi.org/10.1111/j.1469-8137.1991.tb00568.x
  20. Van Etten, H. D. 1976. Antifungal activity of Pterocarpans and other selected isoflavonoid. Phytochemistry 15: 655-659 https://doi.org/10.1016/S0031-9422(00)94414-5

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