Graduate School of Life and Environment Sciences, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8572, Japan.
Graduate School of Life and Environment Sciences, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8572, Japan; Quantum Beam Science Center, Japan Atomic Energy Agency (JAEA), Watanuki 1233, Takasaki, Gunma 370-1292, Japan.
Plant Physiol Biochem. 2015 Nov;96:417-25. doi: 10.1016/j.plaphy.2015.08.021. Epub 2015 Sep 10.
Phosphoenolpyruvate carboxykinase (PEPCK) is a key regulatory enzyme and is utilized in the gluconeogenesis pathway in plants. Although, its catalytic and regulatory properties are quite well understood, there are uncertainties regarding its physiological role in many plants tissues such as the flesh of developing fruits. To further understand the function of PEPCK in fruits and other tissues, RNAi transgenic tomato plants in which SlPEPCK transcription was down-regulated by either CaMV 35S constitutive promoter or the fruit-specific E8 promoter were generated and characterized on the basis of their phenotypic and metabolic aspects. In the PEPCK-deficient lines, prominent growth suppression of germinated seedlings was observed and other vegetative suppression appeared during the early stage of plant growth in the 35S promoter-driven lines. In particular, root elongation was most obviously suppressed in the germinated seedlings, indicating that the gluconeogenesis pathway is involved in the root growth of seedlings. Regarding the primary metabolism in fruit, the soluble sugar content tended to decrease, whereas the malate content tended to increase in ripening fruits of the RNAi lines compared with the wild type. These results indicate that activation of the gluconeogenesis pathway from organic acids to sugars occurs during ripening but is suppressed by the knocking down of the PEPCK gene, suggesting that PEPCK participates in determining the sugar/acid ratio in ripening fruit.
磷酸烯醇式丙酮酸羧激酶(PEPCK)是一种关键的调节酶,在植物的糖异生途径中被利用。尽管其催化和调节特性已经相当清楚,但在许多植物组织中,如发育中的果实的果肉,其生理作用仍存在不确定性。为了进一步了解 PEPCK 在果实和其他组织中的功能,利用 CaMV 35S 组成型启动子或果实特异性 E8 启动子下调 SlPEPCK 转录的 RNAi 转基因番茄植物被生成并基于其表型和代谢方面进行了表征。在 PEPCK 缺陷型系中,观察到萌发幼苗的明显生长抑制,并且在 35S 启动子驱动的系中植物生长的早期出现其他营养生长抑制。特别是在萌发的幼苗中,根伸长受到最明显的抑制,表明糖异生途径参与幼苗的根生长。关于果实中的初级代谢,与野生型相比,RNAi 系的成熟果实中的可溶性糖含量趋于降低,而苹果酸含量趋于增加。这些结果表明,在成熟过程中从有机酸到糖的糖异生途径的激活,但被敲低 PEPCK 基因所抑制,表明 PEPCK 参与决定成熟果实中的糖/酸比。