2014•Scientia HorticulturaeOpen access

Effect of postharvest acibenzolar-S-methyl dipping on phenylpropanoid pathway metabolism in muskmelon (Cucumis melo L.) fruits

Yaoyao Liu, Yonghong Ge, Yang Bi, Canying Li, Huiwen Deng, Lingang Hu, Boyu Dong

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Abstract

Muskmelon (Cucumis melo L. cv. Yujinxiang) fruit were dipped in 0.1 g/L acibenzolar-S-methyl (ASM) solution for 10 min and then stored at room temperature (22 ± 2 °C, relative humidity 55–60%). The results indicated that ASM significantly (P ≤ 0.05) increased the activities of phenylalanine ammonia lyase, tyrosine ammonia lyase, cinnamate-4-hydroxylase, 4-coumarate/coenzyme A ligase, peroxidase, and laccase. ASM also enhanced cinnamic acid dehydrogenase activity. Furthermore, ASM significantly (P ≤ 0.05) enhanced the contents of caffeic acid and ferulic acid, the precursors of lignin biosynthesis, and decreased the content of p-coumaric acid during the late assay time. In addition, significant accumulation of total phenolics, flavonoids and lignin were observed in ASM-treated fruit. These results suggest that ASM treatment activates the phenylpropanoid pathway to enhance the activity of related enzymes as well as the phenylpropanoid content in the fruit to strengthen the cell wall and prevent pathogenic invasion.

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What this paper is about

Muskmelon (Cucumis melo L. cv. Yujinxiang) fruit were dipped in 0.1 g/L acibenzolar-S-methyl (ASM) solution for 10 min and then stored at room temperature (22 ± 2 °C, relative humidity 55–60%). The results indicated that ASM significantly (P ≤ 0.05) increased the activities of phenylalanine ammonia lyase, tyrosine ammonia lyase, cinnamate-4-hydroxylase, 4-coumarate/coenzyme A ligase, peroxidase, and laccase. ASM also enhanced cinnamic acid dehydrogenase activity. Furthermore, ASM significantly (P ≤ 0.05) enhanced the contents of caffeic acid and ferulic acid, the precursors of lignin biosynthesis, and decreased the content of p-coumaric acid during the late assay time. In addition, significant accumulation of total phenolics, flavonoids and lignin were observed in ASM-treated fruit. These results suggest that ASM treatment activates the phenylpropanoid pathway to enhance the activity of related enzymes as well as the phenylpropanoid content in the fruit to strengthen the cell wall and prevent pathogenic invasion.

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Available abstract

Muskmelon (Cucumis melo L. cv. Yujinxiang) fruit were dipped in 0.1 g/L acibenzolar-S-methyl (ASM) solution for 10 min and then stored at room temperature (22 ± 2 °C, relative humidity 55–60%). The results indicated that ASM significantly (P ≤ 0.05) increased the activities of phenylalanine ammonia lyase, tyrosine ammonia lyase, cinnamate-4-hydroxylase, 4-coumarate/coenzyme A ligase, peroxidase, and laccase. ASM also enhanced cinnamic acid dehydrogenase activity. Furthermore, ASM significantly (P ≤ 0.05) enhanced the contents of caffeic acid and ferulic acid, the precursors of lignin biosynthesis, and decreased the content of p-coumaric acid during the late assay time. In addition, significant accumulation of total phenolics, flavonoids and lignin were observed in ASM-treated fruit. These results suggest that ASM treatment activates the phenylpropanoid pathway to enhance the activity of related enzymes as well as the phenylpropanoid content in the fruit to strengthen the cell wall and prevent pathogenic invasion.

Key concepts: Phenylpropanoid, Phenylalanine ammonia-lyase, Cucumis, Cinnamic acid, Chemistry, Phenylalanine, Cinnamyl-alcohol dehydrogenase, Caffeic acid

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Effect of postharvest acibenzolar-S-methyl dipping on phenylpropanoid pathway metabolism in muskmelon (Cucumis melo L.) fruits — Research Paper | ScholarLens