Brummell David A, Dal Cin V, Crisosto Carlos H, Labavitch John M
Department of Plant Sciences, University of California at Davis, One Shields Avenue, Davis, CA 95616, USA.
J Exp Bot. 2004 Sep;55(405):2029-39. doi: 10.1093/jxb/erh227. Epub 2004 Jul 30.
Cell wall changes were examined in fruit of a melting flesh peach (Prunus persica L.) allowed to ripen on the tree. Three phases to softening were noted, the first of which began prior to the completion of flesh colour change and an increase in ethylene evolution. Softening in young mature fruit, prior to ripening, was associated with a depolymerization of matrix glycans both loosely and tightly attached to cellulose and a loss of Gal from all cell wall fractions. After the initiation of ripening, but before the melting stage, softening was associated with continuing, progressive depolymerization of matrix glycans. A massive loss of Ara from the loosely bound matrix glycan fraction was observed, probably from side chains of glucuronoarabinoxylan, pectin, or possibly arabinogalactan protein firmly bound into the wall and solubilized in this extract. An increase in the solubilization of polyuronides also occurred during this period, when softening was already well advanced. The extensive softening of the melting period was marked by substantial depolymerization of both loosely and tightly bound matrix glycans, including a loss of Ara from the latter, an increase in matrix glycan extractability, and a dramatic depolymerization of chelator-soluble polyuronides which continued during senescence. Depolymerization of chelator-soluble polyuronides thus occurred substantially after the increase in their solubilization. Ripening-related increases were observed in the activities of exo- and endo-polygalacturonase (EC 3.2.1.67; EC 3.2.1.15), pectin methylesterase (EC 3.1.1.11), endo-1,4-beta-glucanase (EC 3.2.1.4), endo-1,4-beta-mannanase (EC 3.2.1.78), alpha-arabinosidase (EC 3.2.1.55), and beta-galactosidase (EC 3.2.1.23), but the timing and extent of the increases differed between enzymes and was not necessarily related to ethylene evolution. Fruit softening in peach is a continuous process and correlated closely with the depolymerization of matrix glycans, which proceeded throughout development. However, numerous other cell wall changes also took place, such as the deglycosylation of particular polymers and the solubilization and depolymerization of chelator-soluble polyuronides, but these were transient and occurred only at specific phases of the softening process. Fruit softening and other textural changes in peach appear to have a number of stages, each involving a different set of cell wall modifications.
对树上成熟的溶质型蜜桃(Prunus persica L.)果实的细胞壁变化进行了研究。观察到软化过程分为三个阶段,第一阶段始于果肉颜色变化完成之前,且乙烯释放量增加。未成熟果实成熟前的软化与松散和紧密附着于纤维素的基质聚糖解聚以及所有细胞壁组分中半乳糖(Gal)的损失有关。成熟开始后但在溶质化阶段之前,软化与基质聚糖持续的渐进性解聚有关。观察到从松散结合的基质聚糖组分中大量损失阿拉伯糖(Ara),可能来自葡糖醛酸阿拉伯木聚糖、果胶的侧链,或者可能来自牢固结合在细胞壁中并在该提取物中溶解的阿拉伯半乳聚糖蛋白。在此期间,当软化已经相当明显时,多聚半乳糖醛酸苷的溶解度也增加。溶质化阶段的广泛软化特征是松散和紧密结合的基质聚糖均发生大量解聚,包括后者中Ara的损失、基质聚糖提取率的增加以及螯合剂可溶性多聚半乳糖醛酸苷的剧烈解聚,这种解聚在衰老过程中持续。因此,螯合剂可溶性多聚半乳糖醛酸苷的解聚在其溶解度增加之后大量发生。观察到与成熟相关的外切和内切多聚半乳糖醛酸酶(EC 3.2.1.67;EC 3.2.1.15)、果胶甲酯酶(EC 3.1.1.11)、内切-1,4-β-葡聚糖酶(EC 3.2.1.4)、内切-1,4-β-甘露聚糖酶(EC 3.2.1.78)、α-阿拉伯糖苷酶(EC 3.2.1.55)和β-半乳糖苷酶(EC 3.2.1.23)活性增加,但酶活性增加的时间和程度不同,且不一定与乙烯释放相关。桃果实的软化是一个连续过程,与基质聚糖的解聚密切相关,基质聚糖解聚贯穿整个发育过程。然而,还发生了许多其他细胞壁变化,例如特定聚合物的去糖基化以及螯合剂可溶性多聚半乳糖醛酸苷的溶解和解聚,但这些都是短暂的,仅在软化过程的特定阶段发生。桃果实的软化和其他质地变化似乎有多个阶段,每个阶段涉及不同的一组细胞壁修饰。