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一氧化氮对叶片磷酸烯醇式丙酮酸羧激酶活性的调节:在高粱盐胁迫响应中的意义。

Nitric oxide regulation of leaf phosphoenolpyruvate carboxylase-kinase activity: implication in sorghum responses to salinity.

机构信息

Departamento de Biología Vegetal y Ecología, Facultad de Biología, Universidad de Sevilla, Avenida Reina Mercedes nº 6, 41012, Seville, Spain.

出版信息

Planta. 2013 Nov;238(5):859-69. doi: 10.1007/s00425-013-1933-x. Epub 2013 Aug 3.

Abstract

Nitric oxide (NO) is a signaling molecule that mediates many plant responses to biotic and abiotic stresses, including salt stress. Interestingly, salinity increases NO production selectively in mesophyll cells of sorghum leaves, where photosynthetic C₄ phosphoenolpyruvate carboxylase (C₄ PEPCase) is located. PEPCase is regulated by a phosphoenolpyruvate carboxylase-kinase (PEPCase-k), which levels are greatly enhanced by salinity in sorghum. This work investigated whether NO is involved in this effect. NO donors (SNP, SNAP), the inhibitor of NO synthesis NNA, and the NO scavenger cPTIO were used for long- and short-term treatments. Long-term treatments had multifaceted consequences on both PPCK gene expression and PEPCase-k activity, and they also decreased photosynthetic gas-exchange parameters and plant growth. Nonetheless, it could be observed that SNP increased PEPCase-k activity, resembling salinity effect. Short-term treatments with NO donors, which did not change photosynthetic gas-exchange parameters and PPCK gene expression, increased PEPCase-k activity both in illuminated leaves and in leaves kept at dark. At least in part, these effects were independent on protein synthesis. PEPCase-k activity was not decreased by short-term treatment with cycloheximide in NaCl-treated plants; on the contrary, it was decreased by cPTIO. In summary, NO donors mimicked salt effect on PEPCase-k activity, and scavenging of NO abolished it. Collectively, these results indicate that NO is involved in the complex control of PEPCase-k activity, and it may mediate some of the plant responses to salinity.

摘要

一氧化氮(NO)是一种信号分子,介导植物对生物和非生物胁迫的许多反应,包括盐胁迫。有趣的是,盐度选择性地增加高粱叶片中叶肉细胞中的 NO 产生,其中存在光合 C₄ 磷酸烯醇丙酮酸羧化酶(C₄ PEPCase)。PEPCase 受磷酸烯醇丙酮酸羧化酶激酶(PEPCase-k)调节,盐度极大地增强了高粱中 PEPCase-k 的水平。这项工作研究了 NO 是否参与这种效应。使用 NO 供体(SNP、SNAP)、NO 合成抑制剂 NNA 和 NO 清除剂 cPTIO 进行长期和短期处理。长期处理对 PPCK 基因表达和 PEPCase-k 活性都有多种影响,还降低了光合作用气体交换参数和植物生长。尽管如此,还是可以观察到 SNP 增加了 PEPCase-k 的活性,类似于盐度的影响。NO 供体的短期处理不会改变光合作用气体交换参数和 PPCK 基因表达,但会增加光照下叶片和黑暗中叶片的 PEPCase-k 活性。至少在一定程度上,这些效应独立于蛋白质合成。在 NaCl 处理的植物中,用环己酰亚胺进行短期处理不会降低 PEPCase-k 的活性;相反,cPTIO 会降低其活性。总之,NO 供体模拟了盐度对 PEPCase-k 活性的影响,而 NO 的清除则消除了这种影响。综上所述,NO 参与了 PEPCase-k 活性的复杂调控,它可能介导了植物对盐度的一些反应。

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