Induction of anthocyanins accumulation by methyl jasmonate in shoots of Crassula multicava Lam.

• Autorzy: Saniewski M , Horbowicz M. , Puchalski J.

Warianty tytułu

PL

Indukcja akumulacji antocyjanow przez jasmonian metylu w pedach Crassula multicava Lam.

• Języki publikacji: EN

Abstrakty

EN

In Crassula multicava Lam. anthocyanins are formed naturally mostly in the stem near nodes and only traces in other parts of internodes. Methyl jasmonate (JA-Me) applied in lanolin paste at concentrations of 0.05, 0.1, 0.5 and 1.0% on the middle part of internodes greatly stimulated anthocyanins accumulation in the internodes and in the nodes of Crassula multicava. The stimulatory effect was higher in younger tissues of the Crassula multicava stem than in older ones, and depends on the used concentration of JA-Me. The possible role of jasmonates on anthocyanins formation in Crassula multicava is discussed.

PL

W pędach Crassula multicavaLam. w naturalnych warunkach antocyjany two- rzą się głównie w łodydze w pobliżu węzłów i tylko śladowe ilości w innych czę- ściach międzywężli. Jasmonian metylu (JA-Me) podany w paście lanolinowej w stężeniach 0,05, 0,1, 0,5 i 1,0% w środku poszczególnych międzywężli silnie sty- mulował akumulację antocyjanów w miedzywężlach i węzłach Crassula multicava.Stymulacja ta była większa w młodszych, górnych tkankach pędu niż w starszych i zależna była od stężenia użytego JA-Me. Możliwa rola jasmonianów w akumulacji antocyjanów w pędach Crassula multicava jest dyskutowana.

Słowa kluczowe

EN

accumulation; shoot; flavonoids; anthocyanin; Crassula multicava; methyl jasmonate; stem

• Wydawca: -
• Czasopismo: Acta Agrobotanica
• Rocznik: 2006
• Tom: 59
• Numer: 2
• Opis fizyczny: p.43-50,fig.,ref.

Twórcy

autor

Saniewski M

• Research Institute of Pomology and Floriculture, Pomologiczna 18, 96-100 Skierniewice, Poland

autor

Horbowicz M.

autor

Puchalski J.

Bibliografia

• Ae r t s R. J., Gisi D., D e Carolis E., D e Luca V., Banmann T. W., 1994. Methyl jasmonate vapor increases the developmentally controlled synthesis of alkaloids in Catharanthus and Cinchona seedlings. Plant J. 5: 635 643.
• Blechert S., Brodschelm W., Höylder S., Kammerer L., Kutchan T. M., Muell e r M. J., X i a Z. Q., Zenk M. H., 1995. The octadecanoid pathway: Signal molecules for the regulation of secondary pathways. Proc. Natl. Acad. Sci. USA 92: 4099 4105.
• Creelman R. A., Mullet J. E., 1995. Jasmonic acid distribution and action in plants: Regulation during development and response to biotic and abiotic stress. Proc. Natl. Acad. Sci.USA 92: 4114 4119.
• Creelman R. A., Tierney M. L., Mullet J. E., 1992. Jasmonic acid/methyl jasmonate accumulation in wounded soybean hypocotyls and modulate wound gene expression. Proc. Natl. Acad. Sci. USA, 89: 4938 4941.
• De Bruxelles G. L., Roberts M. R., 2001. Signals regulating multiple responses to wounding and herbivores. Crit. Rev. Plant Sci. 20: 487 521.
• Dittrich H., Kutchan T., Zenk M. H., 1992. The jasmonate precursor, 12 oxo phytodienoicacid, induces phytoalexin synthesis in Petroselinum hortense cell cultures. FEBS Lett. 309: 33 36.
• Fang Y., Smith M. A. L., Pepin M. F., 1999. Effects of exogenous methyl jasmonate inelicited anthocyanin producing cell cultures of ohelo (Vaccinum pahalae). In Vitro Cell Dev. Biol. Plant, 35: 106 113.
• Farmer E. E., Ryan A. C., 1990. Interplant communication: Airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. Proc. Natl. Acad. Sci. USA 87: 7713 7716.
• Feys B. J. F., Benedetti C. E., Penfold C. N., Turner J. G., 1994. Arabidopsis mutants selected for resistance to the phytotoxin coronatine are male sterile, insensitive to methyl jasmonate, and resistant to bacterial pathogens. Plant Cell, 6: 751 759.
• Franceschi V. R., Grimes H. D., 1991. Induction of soybean vegetative proteins and anthocyanin by low level atmospheric methyl jasmonate. Proc. Natl. Acad. Sci. USA 88: 6745 6749.
• Gundlach H., Muller M. J., Kutchan T. M., Zenk M. H., 1992. Jasmonic acid is a signal transducer in elicitor induced plant cell culture. Proc. Natl. Acad. Sci. USA, 89: 2389 2393.
• Kondo S., Tsukada N., Niimi Y., Seto H., 2001. Interactions between jasmonates and abscisic acid in apple fruit, and stimulative effect of jasmonates on anthocyanin accumulation. J. Japan. Soc. Hort. Sci. 70: 546 552.
• Pieterse C. M. J., To n J., Va n Loon L. C., 2001. Cross talk between plant defence signalling pathways: boost or burden? AgBiotechNet, ABN 0698, 3: 1 8.
• Saniewski M., Horbowicz M., Puchalski J., Ueda J., 2003. Methyl jasmonate stimulates the formation and the accumulation of anthocyanin in Kalanchoe blossfeldiana. Acta Physiol. Plant. 25: 143 149.
• Saniewski M., Miszczak A., Kawa Miszczak L., Wêgrzynowicz Lesiak E., Miyamoto K., Ueda J., 1998. Effect of methyl jasmonate on anthocyanin accumulation, ethylene production, and CO2 evolution in uncooled and cooled tulip bulbs. J. Plant Growth. Regul. 17: 33 37.
• Saniewski M., Miyamoto K., Ueda J., 1998. Methyl jasmonate induces gums and stimulates anthocyanin accumulation in peach shoots. J. Plant Growth Regul. 17: 121 124
• Seo H. S., Song J. T., Cheong J. J., Lee Y. W., Hwang I., Lee J. S., Choi Y. D., 2001. Jasmonic acid carboxyl methyltransferase: A key enzyme for jasmonate regulated plant responses. Proc. Natl. Acad. Sci. USA, 98: 4788 4793.
• Swain T., 1965. Analytical methods for flavonoids. Chapter 19. In: Biochemistry of Plant Pigments. T.W. Goodwin (ed)., Academic Press, London, New York, pp. 533 549.
• Tamari G., Borovoch A., Atzorn R., Weiss D., 1995. Methyl jasmonate induces pig mentation and flavonoid gene expression in petunia corollas: A possible role in wound response. Physiol. Plant. 94: 45 50.
• Taylor L. P., Grotewold E., 2005. Flavonoids as developmental regulators. Curr. Opin. Plant Biol. 8: 317 323.
• Winkel Shirley B., 2002. Biosynthesis of flavonoids and effects of stress. Curr. Opin. Plant Biol. 5: 218 223.
• Zhang W., Curtin C., Kikuchi M., Franco C., 2002. Integration of jasmonic acid and light irradiation for enhancement of anthocyanin biosynthesis in Vitis vinifera suspension cultures. Plant Sci. 162: 459 468.