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Changes in cell wall polysaccharides of kiwifruit and the visco-elastic properties detected by a laser Doppler method

机译:激光多普勒法检测猕猴桃细胞壁多糖的变化及粘弹性

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Visco-elastic properties of kiwifruit were measured by a laser Doppler method over an eight day ripening period. After ethylene treatment, fruit flesh elasticity decreased exponentially. However, viscosity of the flesh increased from day 0 to 2 and then decreased. Fruit tissue was boiled in 80% ethanol to extract soluble sugars (EtOH fraction); the EtOH-insoluble residue was treated with alpha -amylase to solubilize starch. The amount of sucrose, glucose, fructose and inositol in the EtOH fraction on unit FW basis increased from day 0 to 3, while starch decreased during the ripening period. Cell wall material was fractionated into the hot water-soluble (WS), hot EDTA-soluble (pectin), alkaline soluble (hemicellulose) and residual (cellulose) fractions. The quantity of hydrolyzed sugars in the WS fraction decreased exponentially during ripening, whereas that in the pectin and hemicellulose fractions increased slightly on day 1 and then decreased rapidly. The amount of cellulose remained nearly constant during ripening. The iodine method revealed appreciable amounts of xyloglucan in the hemicellulose fraction. Gel permeation chromatography of polymers in the hemicellulose fraction revealed that xyloglucan had degraded rapidly by day 2. The molecular weights of both total sugar and uronic acid components of the pectin fraction increased from day 0 to 2, and then decreased. The amount of total cell wall polysaccharides and starch decreased by 80% during ripening, which indicates that a decrease in the molecular weight of xyloglucan correlates with a loss in fruit tissue elasticity, while the changes in the molecular weight of pectin corresponds with changes in viscosity. A substantial portion of the cell wall polysaccharides was hydrolyzed to soluble sugars in the early phase of ripening.
机译:通过激光多普勒方法在八天的成熟期内测量猕猴桃的粘弹性。乙烯处理后,果肉弹性呈指数下降。但是,果肉的粘度从第0天增加到第2天,然后下降。将水果组织在80%乙醇中煮沸以提取可溶性糖(EtOH馏分);将不溶于EtOH的残基用α-淀粉酶处理以溶解淀粉。从第0天到第3天,以单位FW为基础的EtOH馏分中的蔗糖,葡萄糖,果糖和肌醇的量增加,而淀粉在成熟期减少。将细胞壁材料分级为可溶于热水的(WS),可溶于EDTA的(果胶),可溶于碱的(半纤维素)和残留的(纤维素)级分。 WS馏分中的水解糖量在成熟期间呈指数下降,而果胶和半纤维素馏分中的水解糖量在第1天略有增加,然后迅速下降。在成熟过程中,纤维素的量几乎保持恒定。碘法显示半纤维素部分中有相当数量的木葡聚糖。半纤维素馏分中聚合物的凝胶渗透色谱法显示,木葡聚糖在第2天迅速降解。果胶馏分中的总糖和糖醛酸成分的分子量从第0天增加到第2天,然后降低。在成熟过程中,细胞壁多糖和淀粉的总量减少了80%,这表明木葡聚糖的分子量降低与果实组织弹性的下降有关,而果胶分子量的变化与粘度的变化相对应。 。在成熟的早期,大部分细胞壁多糖被水解成可溶性糖。

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