Dicyclohexylcarbodiimide and disodium succinate regulate the browning development in fresh longan pericarp by modulating the antioxidant system and the metabolisms of membrane lipids and phenolics

被引:22
|
作者
Chen, Yazhen [1 ,2 ]
Lin, Hetong [1 ,2 ]
Zhang, Huili [1 ,2 ]
Chen, Yang [1 ,2 ]
Lin, Mengshi [3 ]
Zheng, Yi [1 ,2 ]
Fan, Zhongqi [1 ,2 ]
Wang, Hui [1 ,2 ]
Chen, Yihui [1 ,2 ]
Lin, Yifen [1 ,2 ]
机构
[1] Fujian Agr & Forestry Univ, Inst Postharvest Technol Agr Prod, Coll Food Sci, Fuzhou 350002, Fujian, Peoples R China
[2] Fujian Prov Univ, Fujian Agr & Forestry Univ, Key Lab Postharvest Biol Subtrop Special Agr Prod, Fuzhou 350002, Fujian, Peoples R China
[3] Univ Missouri, Food Sci Program, Div Food Nutr & Exercise Sci, Columbia, MO 65211 USA
基金
中国国家自然科学基金;
关键词
Longan fruit; Pericarp pigments; Browning; Reactive oxygen species; Lipid peroxidation; Phenolic metabolism; HARVESTED LITCHI FRUIT; DISEASE DEVELOPMENT; PROPYL GALLATE; QUALITY; STORAGE;
D O I
10.1016/j.postharvbio.2023.112388
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
In this study, the effects of dicyclohexylcarbodiimide (DCC) and disodium succinate (DS) treatments on the pericarp browning (PB) development in postharvest longan were elucidated by measuring PB-related phenotypes and the metabolisms of antioxidants, membrane lipids, and phenolics. Compared to the control, DCC-treated longan displayed the higher levels of PB index, CMP, ROS, PA, DAG, and SFAs, the higher activities of POD, PPO, and MLMEs including PLD, PC-PLC, PI-PLC, lipase, and LOX, and the higher expression levels of DlPPO1 , DlPOD1 , and genes encoding MLMEs. In contrast, the lower levels of chromaticity values, pigments, TP, PC, PI, and USFAs, the lower activities of RSEs including SOD, CAT, and APX, the lower expression levels of genes encoding RSEs, and a lower non-enzymatic antioxidant capacity were also noted in DCC-treated longan. These results imply that the exacerbated PB induced by DCC was associated with the activation of MLMEs by up -regulating the expression of genes encoding MLMEs, which expedited the damage of cell membrane. This membrane damage was also regulated by the accelerated accumulation of ROS triggered by DCC. The increased membrane permeability after the damage prompted an enzymatic oxidation between phenol oxidase and phe-nolics. However, the opposite effect occurred in the DS-treated longan.
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页数:15
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