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      Deciphering the Metabolic Pathways of Pitaya Peel after Postharvest Red Light Irradiation

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          Abstract

          Red light irradiation can effectively prolong the shelf-life of many fruit. However, little is known about red light-induced metabolite and enzyme activities. In this study, pitaya fruit was treated with 100 Lux red light for 24 h. Red light irradiation significantly attenuated the variation trend of senescence traits, such as the decrease of total soluble solid (TSS) and TSS/acidity (titratable acidity, TA) ratio, the increase of TA, and respiratory rate. In addition, the reactive oxygen species (ROS) related characters, primary metabolites profiling, and volatile compounds profiling were determined. A total of 71 primary metabolites and 67 volatile compounds were detected and successfully identified by using gas chromatography mass spectrometry (GC-MS). Red light irradiation enhanced glycolysis, tricarboxylic acid (TCA) cycle, aldehydes metabolism, and antioxidant enzymes activities at early stage of postharvest storage, leading to the reduction of H 2O 2, soluble sugars, organic acids, and C-6 and C-7 aldehydes. At a later stage of postharvest storage, a larger number of resistance-related metabolites and enzyme activities were induced in red light-treated pitaya peel, such as superoxide dismutase (SOD), ascorbate peroxidase (APX), 1,1-diphenyl-2-picryl-hydrazyl (DPPH) radical-scavenging, reducing power, fatty acids, and volatile aroma.

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          Most cited references43

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          Class III peroxidases in plant defence reactions.

          When plants are attacked by pathogens, they defend themselves with an arsenal of defence mechanisms, both passive and active. The active defence responses, which require de novo protein synthesis, are regulated through a complex and interconnected network of signalling pathways that mainly involve three molecules, salicylic acid (SA), jasmonic acid (JA), and ethylene (ET), and which results in the synthesis of pathogenesis-related (PR) proteins. Microbe or elicitor-induced signal transduction pathways lead to (i) the reinforcement of cell walls and lignification, (ii) the production of antimicrobial metabolites (phytoalexins), and (iii) the production of reactive oxygen species (ROS) and reactive nitrogen species (RNS). Among the proteins induced during the host plant defence, class III plant peroxidases (EC 1.11.1.7; hydrogen donor: H(2)O(2) oxidoreductase, Prxs) are well known. They belong to a large multigene family, and participate in a broad range of physiological processes, such as lignin and suberin formation, cross-linking of cell wall components, and synthesis of phytoalexins, or participate in the metabolism of ROS and RNS, both switching on the hypersensitive response (HR), a form of programmed host cell death at the infection site associated with limited pathogen development. The present review focuses on these plant defence reactions in which Prxs are directly or indirectly involved, and ends with the signalling pathways, which regulate Prx gene expression during plant defence. How they are integrated within the complex network of defence responses of any host plant cell will be the cornerstone of future research.
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            Fatty Acid- and Lipid-Mediated Signaling in Plant Defense.

            Fatty acids and lipids, which are major and essential constituents of all plant cells, not only provide structural integrity and energy for various metabolic processes but can also function as signal transduction mediators. Lipids and fatty acids can act as both intracellular and extracellular signals. In addition, cyclic and acyclic products generated during fatty acid metabolism can also function as important chemical signals. This review summarizes the biosynthesis of fatty acids and lipids and their involvement in pathogen defense.
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              Antioxidant and antiproliferative activities of red pitaya

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                Author and article information

                Journal
                Metabolites
                Metabolites
                metabolites
                Metabolites
                MDPI
                2218-1989
                14 March 2020
                March 2020
                : 10
                : 3
                : 108
                Affiliations
                [1 ]Center of Economic Botany, Core Botanical Gardens, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China; wuqixian@ 123456scbg.ac.cn (Q.W.); wubangcai88@ 123456163.com (T.L.); q-hxia@ 123456scbg.ac.cn (H.Q.); ymjiang@ 123456scbg.ac.cn (Y.J.)
                [2 ]Institute of Fruit Tree Research, Guangdong Academy of Agricultural Sciences, Guangzhou 510600, China; huijun_gao@ 123456aliyun.com
                [3 ]College of Food Science and Technology, Hainan University, Haikou 570228, China; zhangzhengke@ 123456hotmail.com
                Author notes
                [* ]Correspondence: yunze@ 123456scbg.ac.cn ; Tel.: +86-20-37252525
                Author information
                https://orcid.org/0000-0002-4648-9572
                https://orcid.org/0000-0003-3966-7657
                Article
                metabolites-10-00108
                10.3390/metabo10030108
                7143668
                32183356
                0205591c-7430-4f22-bc5a-7a52ed8385af
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 17 January 2020
                : 02 March 2020
                Categories
                Article

                fruit decay,red light,pitaya,primary metabolites,ros-related characters,volatile compounds

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