外源钙和钙抑制剂对苹果成熟过程中抗坏血酸生物合成和循环的影响。

IF 5.7 2区 生物学 Q1 PLANT SCIENCES
Siqi Yan, Jingyi Lv, Sijie Dong, Xin Sun, Yonghong Ge
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引用次数: 0

摘要

抗坏血酸(AsA)是苹果果实中重要的抗氧化剂。l -半乳糖途径被认为是其生物合成的主要途径,而抗坏血酸-谷胱甘肽(AsA-GSH)循环是其循环的主要途径。钙信号对水果成熟至关重要。迄今为止,苹果果实成熟过程中钙信号与AsA代谢之间的关系尚不明确。在这项工作中,采后苹果用氯化钙(CaCl2)、氯丙嗪(CPZ)和乙二醇-双(2-氨基乙醚)-N,N,N‘,N’-四乙酸(EGTA)处理,并在20℃下成熟。结果表明,与对照相比,CaCl2处理保持了果肉硬度,降低了成熟过程中的呼吸速率和乙烯产量。在成熟过程中,降低了过氧化氢(H2O2)和去氢抗坏血酸(DHA)的含量,提高了AsA含量和AsA/DHA比值。该处理还提高了l -半乳糖脱氢酶(GalDH)、l -半乳糖-1,4-内酯脱氢酶(GalLDH)、抗坏血酸过氧化物酶(APX)、脱氢抗坏血酸还原酶(DHAR)和单脱氢抗坏血酸还原酶(MDHAR)的活性。相反,EGTA和CPZ处理显示出截然相反的结果。从苹果基因组中共鉴定出71个参与l -半乳糖和AsA循环途径的基因,其中44个基因在果实组织中特异性表达。定量实时PCR (qPCR)分析显示,除了l-半乳糖-1-磷酸磷酸酶基因MdGPP4和MdMDHAR2的表达不受所有处理的影响外,这些基因的表达在三种处理下均有差异。这些数据表明,钙信号在苹果果实成熟过程中介导AsA代谢中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of exogenous calcium and calcium inhibitors on ascorbic acid biosynthesis and recycling during apple ripening.

Ascorbic acid (AsA) is a crucial antioxidant in apple fruit. The L-galactose pathway is considered the primary route for its biosynthesis, whereas the ascorbate-glutathione (AsA-GSH) cycle is the main route for its recycling. Calcium signaling is essential for fruit ripening. To date, relationships between calcium signaling and AsA metabolism in ripening apple fruit are still undetermined. In this work, postharvest apples were treated with calcium chloride (CaCl2), chlorpromazine (CPZ) and ethylene glycol-bis(2-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA), and ripened at 20 °C. The results indicated that, compared with the controls, CaCl2 treatment maintained flesh firmness and reduced respiration rate and ethylene production during ripening. It reduced contents of hydrogen peroxide (H2O2) and dehydroascorbic acid (DHA) but increased content of AsA and AsA/DHA ratio during ripening. This treatment additionally promoted activities of L-galactose dehydrogenase (GalDH), L-galactono-1,4-lactone dehydrogenase (GalLDH), ascorbate peroxidase (APX), dehydroascorbate reductase (DHAR) and monodehydroascorbate reductase (MDHAR). Conversely, EGTA and CPZ treatments displayed contrasting results. A total of 71 genes involved in L-galactose and AsA recycling pathways were identified from the apple genome, with 44 genes expressed specifically in fruit tissue. Quantitative real-time PCR (qPCR) analysis revealed that the expression of these genes responded differentially to these three treatments, except for one L-galactose-1-phosphate phosphatase gene (MdGPP4) and MdMDHAR2 whose expression was unaffected by all treatments. These data indicated that calcium signaling play a role in mediating AsA metabolism in ripening apple fruit.

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来源期刊
Plant Physiology and Biochemistry
Plant Physiology and Biochemistry 生物-植物科学
CiteScore
11.10
自引率
3.10%
发文量
410
审稿时长
33 days
期刊介绍: Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement. Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB. Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.
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