共查询到17条相似文献,搜索用时 234 毫秒
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细胞壁分解酶与果实软化的关系研究进展 总被引:3,自引:0,他引:3
软化是影响果实采后寿命的重要因素,是果实成熟过程一系列细胞壁酶有序作用的结果。各种酶在不同种类果实成熟与软化过程的表现各有特点。本文针对细胞壁分解相关的各种酶,综述果实成熟与软化过程酶活性变化、酶基因表达的最新研究进展,并推测果实软化的分子机理。 相似文献
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果实成熟衰老过程中软化机理研究进展 总被引:1,自引:0,他引:1
介绍了果实成熟衰老过程中呼吸作用、乙烯释放量、细胞壁超微结构和组分变化,以及与果实软化有关的细胞壁酶的活性变化。多数果实软化是由于细胞壁的破坏,细胞中的果胶溶液化,纤维素解体等。与果实软化相关较为密切的4种细胞壁酶:多聚半乳糖醛酸酶(PG)、β-半乳糖苷酶(β-Gal)、纤维素酶(Cx)和果胶甲酯酶(PME)。为深入研究果实软化机理提供参考。 相似文献
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李属植物果实营养丰富,为人类提供了大量的营养物质,但是其果实采后迅速软化,导致果实品质下降、不耐贮藏及货架期短。为了解李属植物果实成熟软化的研究概况,本研究归纳总结了李属植物果实成熟过程中包括呼吸作用、乙烯释放、品质相关物质变化在内的生理变化,细胞壁结构、物质成分变化、细胞壁降解相关酶在内的细胞壁变化,果实成熟软化相关的基因及果实成熟软化蛋白质组学研究进展,并提出了存在的问题及未来研究趋势。指出目前李属植物果实成熟软化研究集中于果实采收后或贮藏期间细胞壁物质成分、结构变化及细胞壁降解相关酶,如多聚半乳糖醛酸酶、β-半乳糖苷酶等的活性变化,及这些酶的基因克隆、功能分析,指出结合转录组学、蛋白质组学、代谢组学和基因组学等几种组学将是李属植物果实成熟软化研究的发展方向。 相似文献
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L-半胱氨酸盐酸盐处理延缓香蕉果实采后成熟的初步研究 总被引:1,自引:0,他引:1
以"巴西"香蕉为试材,利用0.05%的外源L-半胱氨酸盐酸盐处理,测定常温(24±1)℃贮藏过程中果实硬度、色差、可溶性糖含量及多酚氧化酶(PPO)、过氧化物酶(POD)和果胶裂解酶(PL)活性,初步探索L-半胱氨酸盐酸盐处理延缓香蕉果实成熟的机理。结果表明:0.05%L-半胱氨酸盐酸盐处理能够延缓香蕉果实硬度和果皮H值的下降,并减缓果皮L值和C值以及果肉可溶性糖含量的上升,从而保持贮藏品质;同时,通过抑制果皮PPO和POD活性减缓在贮藏后期的褐变,并抑制果肉PL活性推迟香蕉软化进程。因此,0.05%L-半胱氨酸盐酸盐处理可延缓香蕉果实常温贮藏的成熟进程,具有一定的应用价值。 相似文献
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《分子植物育种》2021,19(18):5994-6002
PrupeSEP1在调节桃果实成熟软化过程中起重要作用,本研究通过PrupeSEP1酵母双杂筛库鉴定得到的互作蛋白PrupeAKR2。为了探究PrupeAKR2在桃果实成熟软化中的作用,本研究将PrupeAKR2在‘中桃5号’果实中瞬时过表达,研究其对果实贮藏期间质地指标,成熟软化相关基因的表达量变化的影响,同时利用酵母双杂交系统验证PrupeAKR2和PrupeSEP1是否存在互作。结果表明,瞬时过表达PrupeAKR2后,与对照(PC2300空载体)相比,果实加快软化。在采后贮藏的前2 d,OE-PrupeAKR2果实中成熟软化相关的PrupeACS1、PrupeACO1、PrupePME、PrupePG21、PrupePG22的表达均被抑制;而OE-PrupeAKR2果实在贮藏的4~10 d PrupeACO1和PrupePME的表达量、在贮藏的8~10 d PrupeACS1和PrupePG21的表达量、以及在贮藏的4~8 d PrupePG22的表达量均显著高于对照果实。酵母双杂交验证表明PrupeAKR2与PrupeSEP1存在互作关系。研究结果表明,桃PrupeAKR2和PrupeSEP1蛋白发生互作,且正向调控果实成熟软化。本研究可为PrupeAKR2调控果实成熟软化提供理论依据,对开展PrupeAKR2功能的深入研究具有重要意义。 相似文献
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研究1-MCP和乙烯利处理对5种秋子梨(20±1)℃常温贮藏期间主要生理及软化相关指标的影响,探讨1-MCP和乙烯利对秋子梨品种软化机理的调控,为控制秋子梨果实后熟软化进程提供理论依据.以南果梨、京白梨、花盖梨、尖把梨和安梨5种秋子梨为试材,分别用浓度为0.5μL/L的1-MCP密闭熏蒸24 h和1.0 g/kg的乙烯利溶液浸泡5 min,比较常温((20±1)℃)贮藏期间果实硬度、可溶性固形物(SSC)、可滴定酸(TA)、维生素C(Vc)、呼吸强度、乙烯释放量等生理品质指标以及水溶性果胶、纤维素、淀粉含量、β-半乳糖苷酶(β-Gal)、淀粉酶(AM)、多聚半乳糖醛酸酶(PG)、纤维素酶(CL)等软化相关指标变化.与对照(CK)组相比,1-MCP处理可明显延缓5种秋子梨果实硬度、水溶性果胶(WSP)、纤维素、呼吸强度、乙烯释放量和淀粉含量的减少,降低了PG、β-Gal、CL、AM酶活性,而乙烯利处理组与对照组差异较小.1-MCP处理可通过抑制细胞壁相关降解酶活性和减少乙烯释放量来减轻细胞壁物质的降解,从而有效延缓秋子梨果实软化进程,而乙烯利对果实贮藏过程中软化和细胞壁降解生理变化无明显影响. 相似文献
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《Postharvest Biology and Technology》2002,24(2):135-145
‘Canino’ apricots and ‘Royal Zee’ plums were treated with 1000 nl l−1 1-methylcyclopropene (1-MCP) at 20 °C for 20 h following harvest before 0 °C storage. After 5 days storage for apricots and 10 days for plums and after 30 days storage for both, fruit were moved to 20 °C for ripening. In addition, apricots were stored for 20 days and then treated with 1-MCP concentrations of 10, 100 and 1000 nl l−1 at removal and held for ripening. Ethylene production and respiration rate, as well as fruit quality of apricots varied with treatment. Ethylene production was efficiently inhibited by 1000 nl l−1 1-MCP in fruit treated after storage but not in fruit treated before storage. Fruit softening was associated with ethylene production and affected by 1-MCP in a concentration dependent manner when treated after storage, while 1-MCP did not affect softening in prestorage treated fruit. The color change of fruit was ethylene-independent and not affected by 1-MCP. Internal flesh browning was decreased by 1-MCP regardless of the concentration when treated after storage, while it was enhanced in fruit treated before storage. Decay development in apricots was decreased by 1-MCP in a concentration dependent manner. Ethylene production and respiration in ‘Royal Zee’ plums was greatly inhibited by 1-MCP during ripening after both short-term (10 day) and long term (30 day) storage. Parameters associated with ripening processes were decreased significantly by 1-MCP, including softening, color change, and loss of titratable acidity. These data demonstrate that 1-MCP has potential to delay ripening of apricots and plums, but the cultivar, maturity of fruit, and time of application must be chosen carefully. It is suggested that 1-MCP is more efficient for extending the shelf life and improving the quality of ‘Canino’ apricots directly marketed or after storage, whereas it might be a potent compound for extending both storage period and shelf life of ‘Royal Zee’ plums. 相似文献
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U. Flitsanov A. Mizrach A. Liberzon M. Akerman G. Zauberman 《Postharvest Biology and Technology》2000,20(3):279-286
The low-temperature storage of avocado affects its subsequent softening process and shelf life. One of the main indices of ripeness in avocado fruit is firmness, which changes during the ripening and softening process. The temperature and duration of storage fundamentally influence the firmness of the stored fruit, and monitoring the softening of fruit enables us to regulate its shelf life. The objective of the present study was to use nondestructive ultrasonic tests to elucidate the influences of storage temperature and time on the softening process of avocado fruit. The attenuation of the ultrasonic waves transmitted through the fruit tissue changes as the fruit passes through the various softening stages during and after low-temperature storage. Four groups of avocados, each stored at a different low temperature, and a control group which was stored at room temperature (20°C) were examined during and after their designated storage times, until they reached full ripeness at room temperature. Nondestructive ultrasonic tests and destructive penetration measurements were carried out in order to determine the attenuation and the tissue firmness, respectively, of the avocados. Statistical analysis showed quite good correlation between the firmness and the ultrasonic attenuation, and their dependence on previous storage time-temperature history. This suggests that the ultrasonic measurements could be used as a nondestructive method of monitoring avocado ripeness during low-temperature storage. 相似文献
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Preclimacteric avocado (Persea americana Mill. cv. Booth 7) fruit were treated with aqueous 1-methylcyclopropene (1-MCP) at 0.93 and 9.3 mmol m−3 and then stored at 20 °C to investigate the effect of 1-MCP on antioxidant systems of mesocarp tissue during ripening. Exposure to 1-MCP concentrations significantly delayed softening and peak ethylene production. 1-MCP significantly delayed accumulation of total soluble phenolics, flavonoids, and total antioxidant capacity although levels eventually reached control fruit maxima. The influence of 1-MCP was more pronounced at the higher concentration. Activities of peroxidase [POD (EC 1.11.1.7)], superoxide dismutase [SOD (EC 1.15.1.1)], catalase [CAT (1.11.1.6)] and l-ascorbate peroxidase [APX (EC 1.11.1.11)] increased during early ripening of control fruit followed by slight (CAT) or significant (POD, APX) declines with further ripening. Increases in activities of all enzymes were delayed in proportion to 1-MCP concentration, and maximum activities attained during ripening were largely unaffected by 1-MCP. Postclimacteric declines in POD and APX were not observed at the higher 1-MCP concentration, possibly reflecting incomplete ripening. The results indicate that changes in antioxidant parameters of avocado fruit are not markedly influenced by 1-MCP but are delayed or altered in proportion to the general suppression of ripening as indicated by ethylene production and fruit softening trends. Together with previously published reports, the data also indicate that the effects of ethylene-action suppression on antioxidant parameters during ripening vary considerably among different fruits. Relationships between antioxidant systems, ethylene and ripening are discussed. 相似文献