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番茄多聚半乳糖醛酸酶β亚基表达的降低会影响果实成熟过程中果胶的溶解和降解。

Reduction of tomato polygalacturonase beta subunit expression affects pectin solubilization and degradation during fruit ripening.

作者信息

Watson C F, Zheng L, DellaPenna D

机构信息

Department of Plant Sciences, University of Arizona, Tucson 85721.

出版信息

Plant Cell. 1994 Nov;6(11):1623-34. doi: 10.1105/tpc.6.11.1623.

Abstract

The developmental changes that accompany tomato fruit ripening include increased solubilization and depolymerization of pectins due to the action of polygalacturonase (PG). Two PG isoenzymes can be extracted from ripe fruit: PG2, which is a single catalytic PG polypeptide, and PG1, which is composed of PG2 tightly associated with a second noncatalytic protein, the beta subunit. Previous studies have correlated ripening-associated increases in pectin solubilization and depolymerization with the presence of extractable PG1 activity, prior to the appearance of PG2, suggesting a functional role for the beta subunit and PG1 in pectin metabolism. To assess the function of the beta subunit, we produced and characterized transgenic tomatoes constitutively expressing a beta subunit antisense gene. Fruit from antisense lines had greatly reduced levels of beta subunit mRNA and protein and accumulated < 1% of their total extractable PG activity in ripe fruit as PG1, as compared with 25% for wild type. Inhibition of beta subunit expression resulted in significantly elevated levels of EDTA-soluble polyuronides at all stages of fruit ripening and a significantly higher degree of depolymerization at later ripening stages. Decreased beta subunit protein and extractable PG1 enzyme activity and increased pectin solubility and depolymerization all cosegregated with the beta subunit antisense transgene in T2 progeny. These results indicate (1) that PG2 is responsible for pectin solubilization and depolymerization in vivo and (2) that the beta subunit protein is not required for PG2 activity in vivo but (3) does play a significant role in regulating pectin metabolism in wild-type fruit by limiting the extent of pectin solubilization and depolymerization that can occur during ripening. Whether this occurs by direct interaction of the beta subunit with PG2 or indirectly by interaction of the beta subunit with the pectic substrate remains to be determined.

摘要

伴随番茄果实成熟的发育变化包括由于多聚半乳糖醛酸酶(PG)的作用,果胶的增溶和去聚合作用增强。从成熟果实中可以提取出两种PG同工酶:PG2,它是一种单一催化性的PG多肽;PG1,它由与第二种非催化性蛋白质β亚基紧密结合的PG2组成。先前的研究将与成熟相关的果胶增溶和去聚合作用的增加与可提取的PG1活性的存在联系起来,这一活性在PG2出现之前就已存在,这表明β亚基和PG1在果胶代谢中具有功能性作用。为了评估β亚基的功能,我们构建并鉴定了组成型表达β亚基反义基因的转基因番茄。与野生型果实成熟时可提取的PG活性总量的25%相比,反义株系果实中β亚基mRNA和蛋白质的水平大幅降低,成熟果实中作为PG1积累的总可提取PG活性不到1%。β亚基表达的抑制导致在果实成熟的所有阶段,EDTA可溶性聚半乳糖醛酸水平显著升高,并且在成熟后期去聚合程度显著更高。在T2后代中,β亚基蛋白质和可提取的PG1酶活性的降低以及果胶溶解度和去聚合作用的增加都与β亚基反义转基因共分离。这些结果表明:(1)PG2在体内负责果胶的增溶和去聚合;(2)β亚基蛋白质在体内PG2活性中不是必需的;(3)但通过限制成熟过程中可能发生的果胶增溶和去聚合程度,在调节野生型果实的果胶代谢中发挥重要作用。这是通过β亚基与PG2的直接相互作用还是通过β亚基与果胶底物的间接相互作用发生,仍有待确定。

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