Polle A
Georg-August Universitaet, Forstbotanisches Institut, Abteilung I, Forstbotanik und Baumphysiologie, Buesgenweg 2, 37077 Goettingen, Germany.
Plant Physiol. 2001 May;126(1):445-62. doi: 10.1104/pp.126.1.445.
The present study introduces metabolic modeling as a new tool to analyze the network of redox reactions composing the superoxide dismutase-ascorbate (Asc)-glutathione (GSH) cycle. Based on previously determined concentrations of antioxidants and defense enzymes in chloroplasts, kinetic properties of antioxidative enzymes, and nonenzymatic rate constants of antioxidants with reactive oxygen, models were constructed to simulate oxidative stress and calculate changes in concentrations and fluxes of oxidants and antioxidants. Simulated oxidative stress in chloroplasts did not result in a significant accumulation of O2*- and H2O2 when the supply with reductant was sufficient. Model results suggest that the coupling between Asc- and GSH-related redox systems was weak because monodehydroascorbate radical reductase prevented dehydroascorbate (DHA) formation efficiently. DHA reductase activity was dispensable. Glutathione reductase was mainly required for the recycling of GSH oxidized in nonenzymatic reactions. In the absence of monodehydroascorbate radical reductase and DHA reductase, glutathione reductase and GSH were capable to maintain the Asc pool more than 99% reduced. This suggests that measured DHA/Asc ratios do not reflect a redox balance related to the Asc-GSH-cycle. Decreases in Asc peroxidase resulted in marked H2O2 accumulation without significant effects on the redox balance of Asc/DHA or GSH/GSSG. Simulated loss of SOD resulted in higher H2O2 production rates, thereby affecting all subsequent steps of the Asc-GSH-cycle. In conclusion, modeling approaches contribute to the theoretical understanding of the functioning of antioxidant systems by pointing out questions that need to be validated and provide additional information that is useful to develop breeding strategies for higher stress resistance in plants.
本研究引入代谢建模作为一种新工具,用于分析构成超氧化物歧化酶 - 抗坏血酸(Asc) - 谷胱甘肽(GSH)循环的氧化还原反应网络。基于先前测定的叶绿体中抗氧化剂和防御酶的浓度、抗氧化酶的动力学特性以及抗氧化剂与活性氧的非酶促速率常数,构建模型以模拟氧化应激并计算氧化剂和抗氧化剂的浓度及通量变化。当还原剂供应充足时,叶绿体中模拟的氧化应激并未导致超氧阴离子(O2*-)和过氧化氢(H2O2)的显著积累。模型结果表明,Asc和GSH相关氧化还原系统之间的耦合较弱,因为单脱氢抗坏血酸自由基还原酶有效地阻止了脱氢抗坏血酸(DHA)的形成。DHA还原酶活性是可有可无的。谷胱甘肽还原酶主要用于非酶促反应中氧化型谷胱甘肽(GSSG)的循环利用。在缺乏单脱氢抗坏血酸自由基还原酶和DHA还原酶的情况下,谷胱甘肽还原酶和GSH能够使抗坏血酸池维持超过99%的还原状态。这表明测得的DHA/Asc比值并不反映与Asc - GSH循环相关的氧化还原平衡。抗坏血酸过氧化物酶的减少导致显著的H2O2积累,但对Asc/DHA或GSH/GSSG的氧化还原平衡没有显著影响。模拟超氧化物歧化酶(SOD)的缺失导致更高的H2O2产生速率,从而影响Asc - GSH循环的所有后续步骤。总之,建模方法通过指出需要验证的问题,有助于从理论上理解抗氧化系统的功能,并提供有助于制定提高植物抗逆性育种策略的额外信息。