State Key Laboratory of Food Nutrition and Safety, Tianjin University of Science and Technology, Tianjin 300457, PR China; Key Laboratory of Food Nutrition and Safety, Ministry of Education, Tianjin University of Science and Technology, Tianjin 300457, PR China; College of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin 300457, PR China.
State Key Laboratory of Food Nutrition and Safety, Tianjin University of Science and Technology, Tianjin 300457, PR China; Key Laboratory of Food Nutrition and Safety, Ministry of Education, Tianjin University of Science and Technology, Tianjin 300457, PR China; College of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin 300457, PR China.
Int J Biol Macromol. 2023 Jun 15;240:124356. doi: 10.1016/j.ijbiomac.2023.124356. Epub 2023 Apr 7.
This study aimed to investigate the effect of custard apple cell wall polysaccharides-disassembling on postharvest fruit softening and to explore its key metabolic pathways and gene expression. Custard apple fruit was stored at 15 ± 0.5 °C for 12 days, it was found that the decreased significantly in fruit firmness, contents of NaCO-soluble pectin, hemicellulose and cellulose, and the increased significantly in water-soluble pectin and CDTA-soluble pectin. The activities of cell wall-degrading relevant enzymes in fruit were improved significantly during storage, including cellulase, polygalacturonase, pectin methyl esterase, neutral xylanase, β-galactosidase, and β-D-glucosidase. The RNA sequencing results revealed 41,545 nonredundant unigenes and 7571 differentially expressed genes (DEGs) in custard apple fruit samples. Functional annotation and DEGs data revealed cell wall degradation potentially involved in starch and sucrose metabolism, amino sugar and nucleotide sugar metabolism, galactose metabolism, pentose and glucuronate interconversions. Specifically, two EG and six β-Glc genes controlled the cellulose decomposition, and one β-xyl and one GATU genes involved in the degradation of hemicellulose, and two PME, one Pel, and four PG genes were the major regulators of pectin disassembling. These results provide a molecular foundation for explaining fruit softening and extending shelf life of custard apple.
本研究旨在探讨番荔枝细胞壁多糖降解对采后果实软化的影响,并探讨其关键代谢途径和基因表达。将番荔枝果实贮藏在 15±0.5°C 下 12 天,发现果实硬度、NaCO 可溶性果胶、半纤维素和纤维素含量显著降低,水溶性果胶和 CDTA 可溶性果胶含量显著增加。贮藏过程中果实细胞壁降解相关酶的活性显著提高,包括纤维素酶、多聚半乳糖醛酸酶、果胶甲酯酶、中性木聚糖酶、β-半乳糖苷酶和β-D-葡萄糖苷酶。RNA 测序结果显示,番荔枝果实样品中有 41545 个非冗余的 unigenes 和 7571 个差异表达基因(DEGs)。功能注释和 DEGs 数据显示,细胞壁降解可能参与淀粉和蔗糖代谢、氨基糖和核苷酸糖代谢、半乳糖代谢、戊糖和葡萄糖醛酸转化。具体来说,两个 EG 和六个β-Glc 基因控制纤维素分解,一个β-xyl 和一个 GATU 基因参与半纤维素的降解,两个 PME、一个 Pel 和四个 PG 基因是果胶分解的主要调控因子。这些结果为解释果实软化和延长番荔枝货架期提供了分子基础。