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Advances in metabolism and genetic control of astringency in persimmon (Diospyros kaki Thunb.) fruit: A review

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SCIENTIA HORTICULTURAE
卷 308, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.scienta.2022.111561

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Tannins; Proanthocyanidin; Shikimate pathway; Acetaldehyde; Deastringency

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This review summarizes the advances in the metabolism of astringency in persimmon fruit. Astringency is mainly caused by the formation of complexes between proanthocyanidins and saliva proteins. Different persimmon cultivars have different metabolic pathways for astringency removal. Acetaldehyde is identified as the key compound in the reduction of astringency, and enzymes and transport proteins play important roles in this process. Astringency removal can be achieved through postharvest treatments that induce the synthesis of acetaldehyde by the fruit.
Persimmon fruits accumulate proanthocyanidins during development. Proanthocyanidins form insoluble com-plexes with saliva proteins, which promote a sensation of dryness in the mouth called astringency. Persimmon cultivars are classified according to pollination and the presence of astringency at harvest. The different char-acteristics between persimmon cultivars lead to different metabolic pathways for the loss of astringency. The aim of this review is to gather information about the advances in the literature on the metabolism of astringency in persimmon fruit. Persimmon proanthocyanidins are mostly catechins or epicatechins, biosynthesized from substrates of the shikimic acid pathway, via biosynthetic pathways of phenylpropanoids and flavonoids, from gallic acid units, or from precursors of the anthocyanin pathway. Two enzymes have been identified as key enzymes to this pathway: leucoanthocyanidin reductase and anthocyanidin reductase. Non-astringent cultivars accumulate proanthocyanidins during fruit development, however, the expression of genes that encode essential enzymes of the biosynthetic pathway is reduced in the early stages, interrupting the accumulation of proan-thocyanidins. Acetaldehyde is the responsible compound for the polymerization of proanthocyanidins and the consequent reduction of astringency. In certain non-astringent cultivars, proanthocyanidins are polymerized by acetaldehyde in the final stages of fruit development and transported to the vacuole, blocking the biosynthetic pathway. Two transport proteins, GST and MATE, are supposed to be essential in this process. In other non -astringent cultivars, the loss of astringency can happen due to the dilution of proanthocyanidins as a result of the increase in fruit volume. The removal of astringency in astringent cultivars occurs through the application of postharvest treatments that induce the synthesis of acetaldehyde by the fruit. Exposure to ethylene, high CO2 concentration or ethanol are the most used technologies for this purpose. Despite the advances made in the last decade, the astringency metabolism is complex and involves several metabolic pathways that still need to be elucidated for a better understanding of the effects of astringency removal in persimmon fruit.

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