Department of Scientific and Industrial Research, DSIR Fruit and Trees, Mt. Albert Research Centre, Private Bag, Auckland, New Zealand.
Plant Physiol. 1992 Jan;98(1):71-81. doi: 10.1104/pp.98.1.71.
Pectic polysaccharides solubilized in vivo during ripening, were isolated using phenol, acetic acid, and water (PAW) from the outer pericarp of kiwifruit (Actinidia deliciosa [A. Chev.] C.F. Liang and A.R. Ferguson var deliciosa ;Hayward') before and after postharvest ethylene treatment. Insoluble polysaccharides of the cell wall materials (CWMs) were solubilized in vitro by chemical extraction with 0.05 molar cyclohexane-trans-1,2-diamine tetraacetate (CDTA), 0.05 molar Na(2)CO(3), 6 molar guanidinium thiocyanate, and 4 molar KOH. The Na(2)CO(3)-soluble fraction decreased by 26%, and the CDTA-soluble fraction increased by 54% 1 day after ethylene treatment. Concomitantly, an increase in the pectic polymer content of the PAW-soluble fraction occurred without loss of galactose from the cell wall. The molecular weight of the PAW-soluble pectic fraction 1 day after ethylene treatment was similar to that of the Na(2)CO(3)-soluble fraction before ethylene treatment. Four days after ethylene treatment, 60% of cell wall polyuronide was solubilized, and 50% of the galactose was lost from the CWM, but the degree of galactosylation and molecular weight of pectic polymers remaining in the CWMs did not decrease. The exception was the CDTA-soluble fraction which showed an apparent decrease in molecular weight during ripening. Concurrently, the PAW-soluble pectic fraction showed a 20-fold reduction in molecular weight. The results suggest that considerable solubilization of the pectic polymers occurred during ripening without changes to their primary structure or degree of polymerization. Following solubilization, the polymers then became susceptible to depolymerization and degalactosidation. Pectolytic enzymes such as endopolygalacturonase and beta-galactosidase were therefore implicated in the degradation of solubilized cell wall pectic polymers but not the initial solubilization of the bulk of the pectic polymers in vivo.
在成熟过程中体内溶解的果胶多糖,是从猕猴桃(Actinidia deliciosa [A. Chev.] C.F. Liang 和 A.R. Ferguson var deliciosa ; Hayward')外种皮用苯酚、乙酸和水(PAW)提取的,在采后乙烯处理前后进行分离。细胞壁材料(CWMs)的不溶性多糖通过化学提取用 0.05 摩尔环己烷-反-1,2-二胺四乙酸(CDTA)、0.05 摩尔 Na(2)CO(3)、6 摩尔硫氰酸胍和 4 摩尔 KOH 进行体外溶解。乙烯处理 1 天后,Na(2)CO(3)可溶部分减少 26%,CDTA 可溶部分增加 54%。同时,PAW 可溶部分果胶聚合物含量增加,而细胞壁中半乳糖没有损失。乙烯处理 1 天后 PAW 可溶果胶部分的分子量与乙烯处理前 Na(2)CO(3)可溶部分的分子量相似。乙烯处理 4 天后,60%的细胞壁聚半乳糖醛酸被溶解,50%的半乳糖从 CWMs 中丢失,但果胶聚合物的酯化度和分子量在 CWMs 中没有降低。例外的是 CDTA 可溶部分在成熟过程中分子量明显下降。同时,PAW 可溶果胶部分的分子量减少了 20 倍。结果表明,果胶聚合物在成熟过程中发生了相当大的溶解,但其一级结构或聚合度没有改变。溶解后,聚合物变得容易解聚和去半乳糖化。因此,果胶酶如内切多聚半乳糖醛酸酶和β-半乳糖苷酶参与了溶解的细胞壁果胶聚合物的降解,但不参与体内大部分果胶聚合物的初始溶解。