Compared with the P. longanae-infected longan, the DNP-treated P. longanae-infected fruit represented a higher pulp breakdown index, a higher O2 -. production rate, and a higher MDA content, but the lower activities of APX, SOD and CAT, the lower transcript levels of DlAPX6, DlSOD1, DlSOD2, DlSOD3 and DlCAT1, the lower values of AsA, GSH, flavonoid and total phenolics, a lower scavenging ability of DPPH radical, and a lower value of reducing power. Whereas, the ATP-treated P. longanae-infected samples showed the contrary results. The above findings indicated that the DNP-promoted the pulp breakdown in P. longanae-infected longan was because DNP weakened the capacity of scavenging ROS, raised the O2 -. level, and accelerated the membrane lipids peroxidation. However, the ATP-suppressed the pulp breakdown in P. longanae-infected longan was because ATP improved the capacity of scavenging ROS, reduced the O2 -. level, and reduced the membrane lipids peroxidation.
Keywords: 2,4-Dinitrophenol (DNP); APX, ascorbate peroxidase; ASA, acetylsalicylic acid; ASM, acibenzolar-S-methyl; ATP, adenosine triphosphate; Adenosine triphosphate (ATP); AsA, ascorbic acid; CAT, catalase; CE, catechin equivalent; DHEA, dehydroepiandrosterone; DNP, 2,4-dinitrophenol; DPPH, 1,1-diphenyl-2-picrylhydrazyl; DlSOD, DlCAT, and DlAPX denotes the gene of SOD, CAT, and APX in longan pulp, separately; GAE, gallic acid equivalent; GSH, glutathione; H2O2, hydrogen peroxide; Longan fruit; MDA, malondialdehyde; Membrane lipids peroxidation; NaClO, sodium hypochlorite; O2–., superoxide anion; P. longanae, Phomopsis longanae Chi; Phomopsis longanae Chi; Pulp breakdown; RH, relative humidity; RNA, ribose nucleic acid; ROS metabolism; ROS, reactive oxygen species; RSEs, ROS-scavenging enzymes; Reactive oxygen species (ROS); SDW, sterile distilled water; SOD, superoxide dismutase; cDNA, complementary deoxyribo nucleic acid; ·OH, hydroxyl radical.
© 2022 The Authors.