cis-Jasmone induces accumulation of defence compounds in wheat, Triticum aestivum |
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Authors: | Moraes Maria C Blassioli Birkett Michael A Gordon-Weeks Ruth Smart Lesley E Martin Janet L Pye Barry J Bromilow Richard Pickett John A |
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Affiliation: | a Embrapa Genetic Resources and Biotechnology, Cx. Postal: 02372, Cep. 70849-970 Brasília-DF, Brazil b Biological Chemistry Department, Rothamsted Research, Harpenden, Herts. AL5 2JQ, United Kingdom |
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Abstract: | Liquid phase extraction (LPE) and vapor phase extraction (VPE) methodologies were used to evaluate the impact of the plant activator, cis-jasmone, on the secondary metabolism of wheat, Triticum aestivum, var. Solstice. LPE allowed the measurement of benzoxazinoids, i.e. 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one (DIMBOA), 2-hydroxy-7-methoxy-1,4-benzoxazin-3-one (HMBOA) and 6-methoxy-benzoxazolin-2-one (MBOA), and phenolic acids such as trans-p-coumaric acid, syringic acid, p-hydroxybenzoic acid, vanillic acid and cis- and trans-ferulic acid. Using LPE, a significantly higher level of DIMBOA was found in aerial parts and roots of T. aestivum following treatment with cis-jasmone, when compared with untreated plants. Similar results were obtained for phenolic acids, such as trans-ferulic acid and vanillic acid in roots. Using VPE, it was possible to measure levels of 2-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one (HBOA), benzoxazolin-2(3H)-one (BOA), ferulic acid, syringic acid and coumaric acid. The levels of HBOA in aerial parts and roots were significantly greater in cis-jasmone treated plants compared to untreated plants. cis-Jasmone is known to be a plant activator in terms of production of defence-related volatile semiochemicals that repel aphids and increase the foraging activity of aphid parasitoids. These results show, for the first time, that cis-jasmone also induces selective production of secondary metabolites that are capable of directly reducing development of pests, diseases and weeds. |
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Keywords: | BOA, benzoxazolin-2(3H)-one HBOA, 2-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one DIBOA, 2,4-dihydroxy-(2H)-1,4-benzoxazin-3(4H)-one DIMBOA, 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one MBOA, 6-methoxy-benzoxazolin-2(3H)-one HMBOA, 2-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one PHB, p-hydroxybenzoic acid VAN, vanillic acid SYR, syringic acid cis-FER, cis-ferulic acid trans-p-COU, trans-p-coumaric acid trans-FER, trans-ferulic acid |
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