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Contribution of Malate and Amino Acid Metabolism to Cytoplasmic pH Regulation in Hypoxic Maize Root Tips Studied Using Nuclear Magnetic Resonance Spectroscopy

机译:利用核磁共振波谱研究低氧玉米根尖中苹果酸和氨基酸代谢对细胞质pH调节的贡献

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摘要

31P-, 13C-, and 15N-nuclear magnetic resonance spectroscopy were used to determine the roles of malate, succinate, Ala, Asp, Glu, Gln, and γ-aminobutyrate (GABA) in the energy metabolism and regulation of cytoplasmic pH in hypoxic maize (Zea mays L.) root tips. Nitrogen status was manipulated by perfusing root tips with ammonium sulfate prior to hypoxia; this pretreatment led to enhanced synthesis of Ala early in hypoxia, and of GABA at later times. We show that: (a) the ability to regulate cytoplasmic pH during hypoxia is not significantly affected by enhanced Ala synthesis. (b) Independent of nitrogen status, decarboxylation of Glu to GABA is greatest after several hours of hypoxia, as metabolism collapses. (c) Early in hypoxia, cytoplasmic malate is in part decarboxylated to pyruvate (leading to Ala, lactate, and ethanol), and in part converted to succinate. It appears that activation of malic enzyme serves to limit cytoplasmic acidosis early in hypoxia. (d) Ala synthesis in hypoxic root tips under these conditions is due to transfer of nitrogen ultimately derived from Asp and Gln, present in oxygenated tissue. We describe the relative contributions of glycolysis and malate decarboxylation in providing Ala carbons. (e) Succinate accumulation during hypoxia can be attributed to metabolism of Asp and malate; this flux to succinate is energetically negligible. There is no detectable net flux from Glc to succinate during hypoxia. The significance of the above metabolic reactions relative to ethanol and lactate production, and to flooding tolerance, is discussed. The regulation of the patterns of metabolism during hypoxia is considered with respect to cytoplasmic pH and redox state.
机译:使用 31 P-, 13 C-和 15 N核磁共振波谱法确定苹果酸,琥珀酸,丙氨酸, Asp,Glu,Gln和γ-氨基丁酸(GABA)在低氧玉米(Zea mays L.)根尖的能量代谢和细胞质pH的调节中。缺氧前通过在根尖灌入硫酸铵来控制氮素状态。这种预处理导致缺氧早期增强Ala合成,而后期导致GABA合成增强。我们显示:(a)缺氧期间调节细胞质pH的能力不受增强的Ala合成影响。 (b)与氮的状态无关,缺氧几个小时后,Glu脱羧成GABA的作用最大,这是因为代谢崩溃。 (c)在缺氧的早期,胞质苹果酸被部分脱羧为丙酮酸(导致丙氨酸,乳酸和乙醇),部分被转化为琥珀酸。看来苹果酸酶的活化可在缺氧早期限制细胞质酸中毒。 (d)在这些条件下,低氧根尖中的Ala合成归因于氧的组织中最终来自Asp和Gln的氮的转移。我们描述了糖酵解和苹果酸脱羧在提供Ala碳中的相对贡献。 (e)缺氧期间琥珀酸盐的积累可归因于Asp和苹果酸的代谢;琥珀酸盐的这种通量在能量上可以忽略不计。在缺氧期间,没有检测到从Glc到琥珀酸盐的净通量。讨论了上述代谢反应相对于乙醇和乳酸的产生以及对水淹耐受性的重要性。考虑到细胞质的pH和氧化还原状态,对缺氧期间新陈代谢模式的调节。

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