Jacoby R P, Che-Othman M H, Millar A H, Taylor N L
ARC Centre of Excellence in Plant Energy Biology, M316, The University of Western Australia, Crawley, WA, 6009, Australia.
Botanical Institute and Cluster of Excellence on Plant Sciences (CEPLAS), University of Cologne, Cologne, 50674, Germany.
Plant Cell Environ. 2016 Apr;39(4):823-33. doi: 10.1111/pce.12653. Epub 2015 Dec 11.
A number of previous studies have documented the gross response of mitochondrial respiration to salinity treatment, but it is unclear how NaCl directly affects the kinetics of plant phosphorylating and non-phosphorylating electron transport pathways. This study investigates the direct effects of NaCl upon different respiratory pathways in wheat, by measuring rates of isolated mitochondrial oxygen consumption across different substrate oxidation pathways in saline media. We also profile the abundance of respiratory proteins by using targeted selected reaction monitoring (SRM) mass spectrometry of mitochondria isolated from control and salt-treated wheat plants. We show that all pathways of electron transport were inhibited by NaCl concentrations above 400 mM; however electron transfer chains showed divergent responses to NaCl concentrations between 0 and 200 mM. Stimulation of oxygen consumption was measured in response to NaCl in scenarios where exogenous NADH was provided as substrate and electron flow was coupled to the generation of a proton gradient across the inner membrane. Protein abundance measurements show that several enzymes with activities less affected by NaCl are induced by salinity, whereas enzymes with activities inhibited by NaCl are depleted. These data deepen our understanding of how plant respiration responds to NaCl, offering new mechanistic explanations for the divergent salinity responses of whole-plant respiratory rate in the literature.
此前的多项研究记录了线粒体呼吸对盐度处理的总体反应,但尚不清楚氯化钠如何直接影响植物磷酸化和非磷酸化电子传递途径的动力学。本研究通过测量盐溶液中不同底物氧化途径下分离的线粒体氧气消耗速率,研究了氯化钠对小麦不同呼吸途径的直接影响。我们还通过对从对照和盐处理小麦植株中分离的线粒体进行靶向选择反应监测(SRM)质谱分析,来分析呼吸蛋白的丰度。我们发现,氯化钠浓度高于400 mM时,所有电子传递途径均受到抑制;然而,电子传递链对0至200 mM氯化钠浓度的反应存在差异。在外源NADH作为底物且电子流与跨内膜质子梯度的产生相偶联的情况下,测量到氯化钠刺激了氧气消耗。蛋白质丰度测量结果表明,盐度诱导了几种活性受氯化钠影响较小的酶,而活性受氯化钠抑制的酶则减少。这些数据加深了我们对植物呼吸如何响应氯化钠的理解,为文献中全株呼吸速率不同盐度响应提供了新的机理解释。