Yabuta Yukinori, Mieda Takahiro, Rapolu Madhusudhan, Nakamura Ayana, Motoki Takashi, Maruta Takanori, Yoshimura Kazuya, Ishikawa Takahiro, Shigeoka Shigeru
Department of Advanced Bioscience, Faculty of Agriculture, Kinki University, 3327-204 Nakamachi, Nara, Japan.
J Exp Bot. 2007;58(10):2661-71. doi: 10.1093/jxb/erm124. Epub 2007 Jun 22.
It has been known that leaves exposed to high light contain more L-ascorbic acid (AsA) than those in the shade. However, the mechanism of the light regulation of the AsA pool size in plants is largely unknown. In this work, the relationship between gene expression levels related to AsA biosynthesis and photosynthesis have been studied. When 2-week-old Arabidopsis plants grown under a 16 h daily photoperiod were moved into the dark, the AsA level in the leaves was decreased by 91% in 72 h, whereas it increased by 171% in the leaves of plants exposed to continuous light during the same period. Among the several enzymes of the AsA biosynthesis pathway, the transcript levels of GDP-D-mannose pyrophosphorylase, L-galactose 1-P phosphatase, L-galactono-1,4-lactone dehydrogenase, and the VTC2 gene were down-regulated in the dark. Treatment with inhibitors of photosynthesis, 3-(3,4-dichlorophenyl)-1,1-dimethylurea and atrazine, arrested a rise in the AsA pool size accompanying the decrease in the transcript levels of the genes of the above enzyme in the leaves. When the plants were transferred to a medium containing 0.5% (w/v) sucrose, the photosynthesis activities and the leaf AsA levels were lowered even under exposure to light compared with those in plants on the medium without sucrose. In contrast, the AsA level in leaves of the sugar-insensitive Arabidopsis mutant abi4/sun6 was unaffected by external sucrose. No significant difference in the expression profiles for AsA biosynthesis enzymes was observed between the wild-type and mutant plants by sucrose feeding. The results suggest that photosynthetic electron transport of chloroplasts is closely related to AsA pool size regulation in leaves.
已知暴露在强光下的叶片比处于阴凉处的叶片含有更多的L-抗坏血酸(AsA)。然而,植物中AsA库大小的光调节机制在很大程度上尚不清楚。在这项工作中,研究了与AsA生物合成和光合作用相关的基因表达水平之间的关系。当在每日16小时光周期下生长2周的拟南芥植株移入黑暗中时,叶片中的AsA水平在72小时内下降了91%,而在同一时期暴露于连续光照下的植株叶片中AsA水平增加了171%。在AsA生物合成途径的几种酶中,GDP-D-甘露糖焦磷酸化酶、L-半乳糖1-P磷酸酶、L-半乳糖内酯脱氢酶和VTC2基因的转录水平在黑暗中下调。用光合作用抑制剂3-(3,4-二氯苯基)-1,1-二甲基脲和莠去津处理,阻止了随着叶片中上述酶基因转录水平下降而伴随的AsA库大小的增加。当植株转移到含有0.5%(w/v)蔗糖的培养基中时,与不含蔗糖培养基上的植株相比,即使在光照下,光合作用活性和叶片AsA水平也会降低。相反,对蔗糖不敏感的拟南芥突变体abi4/sun6叶片中的AsA水平不受外源蔗糖的影响。通过蔗糖饲喂,野生型和突变体植株之间未观察到AsA生物合成酶表达谱的显著差异。结果表明,叶绿体的光合电子传递与叶片中AsA库大小的调节密切相关。