2019
DOI: 10.1016/j.postharvbio.2018.10.018
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Influence of fruit stalk on reactive oxygen species metabolism and quality maintenance of peach fruit under chilling injury condition

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Cited by 27 publications
(13 citation statements)
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“…The over-production of O 2 − (the intermediate product of membrane lipid peroxidation) leads to oxidation in cells and causes degradation of lipids, which increases the MDA content in cells [3,[25][26][27]. In our study, the O 2 − content of BFN and BFA showed no significant differences, which indicates that at the beginning of sunburn injury, the higher scavenging effect in the pericarp cells overcomes the increasing concentrations of ROS [28]. The O 2 − content of BFB was significantly higher than that of BFN and BFA, which can be corelated to the fact that with increasing stress conditions, the ability of cells to scavenge ROS decreases and results in cell membrane degradation [26,29,30].…”
Section: Discussioncontrasting
confidence: 48%
“…The over-production of O 2 − (the intermediate product of membrane lipid peroxidation) leads to oxidation in cells and causes degradation of lipids, which increases the MDA content in cells [3,[25][26][27]. In our study, the O 2 − content of BFN and BFA showed no significant differences, which indicates that at the beginning of sunburn injury, the higher scavenging effect in the pericarp cells overcomes the increasing concentrations of ROS [28]. The O 2 − content of BFB was significantly higher than that of BFN and BFA, which can be corelated to the fact that with increasing stress conditions, the ability of cells to scavenge ROS decreases and results in cell membrane degradation [26,29,30].…”
Section: Discussioncontrasting
confidence: 48%
“…The O 2 − content was measured following the method of Li et al. (2019). Briefly, 1.0 mL peach juice was incubated with 1.0 mL reaction mixture containing 0.5 mL phosphate buffer (50.0 mM, pH = 7.8) and 0.5 mL hydroxylamine hydrochloride (10.0 mM) at 25°C for 0.5 h. Then 1.0 mL sulfanilic acid (17.0 mM) and 1.0 mL α‐naphthol (7.0 mM) were added and incubated for another 15 min at 25°C, and the absorption was recorded at 530 nm.…”
Section: Methodsmentioning
confidence: 99%
“…Various in vitro ROS trapping assays exist for evaluating the oxidant scavenging capacity of biological samples. For instance, the hydroxyl radical scavenging activity of a range of biological samples such as chicken skin enzymatic protein hydrolysates [ 30 ] and peach fruit extracts [ 31 ] has been evaluated using a method proposed by de Avellar et al [ 32 ]. This method is based on the production of hydroxyl radicals in the Fenton reaction following the combination of hydrogen peroxide with 1,10-phenanthroline and ferrous ammonium sulfate.…”
Section: Principles Of Chemical Antioxidant Assaysmentioning
confidence: 99%