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
Abstract
Yaoyao Liu, Yonghong Ge, Yang Bi, Canying Li, Huiwen Deng, Lingang Hu, Boyu Dong
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.
OpenAlex reports 143 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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