Department of Biochemistry, University of California, Riverside, California 92521.
Plant Physiol. 1992 Feb;98(2):480-7. doi: 10.1104/pp.98.2.480.
(31)P-, (13)C-, and (15)N-nuclear magnetic resonance spectroscopy were used to determine the roles of malate, succinate, Ala, Asp, Glu, Gln, and gamma-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.
(31)P、(13)C 和(15)N 核磁共振波谱被用于确定苹果酸、琥珀酸、丙氨酸、天冬氨酸、谷氨酸、谷氨酰胺和γ-氨基丁酸(GABA)在缺氧玉米(Zea mays L.)根尖的能量代谢和细胞质 pH 调节中的作用。氮素状况通过在缺氧前用硫酸铵灌注根尖来操纵;这种预处理导致在缺氧早期丙氨酸的合成增强,而在后期 GABA 的合成增强。我们表明:(a)在缺氧期间调节细胞质 pH 的能力不受增强的丙氨酸合成的显著影响。(b)独立于氮素状况,谷氨酸的脱羧作用在缺氧数小时后最大,因为代谢崩溃。(c)在缺氧早期,细胞质中的苹果酸部分脱羧为丙酮酸(导致丙氨酸、乳酸和乙醇),部分转化为琥珀酸。似乎苹果酸酶的激活有助于在缺氧早期限制细胞质酸中毒。(d)在这些条件下缺氧根尖中丙氨酸的合成归因于最终源自天冬氨酸和谷氨酰胺的氮的转移,这些氮源存在于氧合组织中。我们描述了糖酵解和苹果酸脱羧作用在提供丙氨酸碳方面的相对贡献。(e)缺氧期间琥珀酸的积累可归因于天冬氨酸和苹果酸的代谢;这种流向琥珀酸的通量在能量上可以忽略不计。在缺氧期间没有检测到葡萄糖向琥珀酸的净通量。上述代谢反应相对于乙醇和乳酸的产生以及耐淹水能力的意义将被讨论。细胞质 pH 和氧化还原状态被考虑用于缺氧期间代谢模式的调节。