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实验和模型数据与在细胞色素氧化酶的临界氧分压以上的内部[O2]水平下植物组织呼吸下调的观点相矛盾。

Experimental and modelling data contradict the idea of respiratory down-regulation in plant tissues at an internal [O2] substantially above the critical oxygen pressure for cytochrome oxidase.

机构信息

Department of Biological Sciences, University of Hull, Kingston upon Hull, UK.

出版信息

New Phytol. 2011 Apr;190(2):431-41. doi: 10.1111/j.1469-8137.2010.03537.x. Epub 2010 Nov 30.

DOI:10.1111/j.1469-8137.2010.03537.x
PMID:21118258
Abstract

• Some recent data on O(2) scavenging by root segments showed a two-phase reduction in respiration rate starting at/above 21 kPa O(2) in the respirometer medium. The initial decline was attributed to a down-regulation of respiration, involving enzymes other than cytochrome oxidase, and interpreted as a means of conserving O(2). As this appeared to contradict earlier findings, we sought to clarify the position by mathematical modelling of the respirometer system. • The Fortran-based model accommodated the multicylindrical diffusive and respiratory characteristics of roots and the kinetics of the scavenging process. Output included moving images and data files of respiratory activity and [O(2)] from root centre to respirometer medium. • With respiration at any locus following a mitochondrial cytochrome oxidase O(2) dependence curve (the Michaelis-Menten constant K(m) = 0.0108 kPa; critical O(2) pressure, 1-2 kPa), the declining rate of O(2) consumption proved to be biphasic: an initial, long semi-linear part, reflecting the spread of severe hypoxia within the stele, followed by a short curvilinear fall, reflecting its extension through the pericycle and cortex. • We conclude that the initial respiratory decline in root respiration recently noted in respirometry studies is attributable to the spread of severe hypoxia from the root centre, rather than a conservation of O(2) by controlled down-regulation of respiration based on O(2) sensors.

摘要

• 最近有一些关于根段清除 O(2)的资料显示,在呼吸计介质中,当 O(2)分压达到/高于 21 kPa 时,呼吸速率开始呈现两阶段下降。最初的下降归因于呼吸的下调,涉及细胞色素氧化酶以外的酶,被解释为一种节约 O(2)的手段。由于这似乎与早期的发现相矛盾,我们试图通过呼吸计系统的数学建模来澄清这一观点。 • 该基于 Fortran 的模型适应了根的多圆柱扩散和呼吸特性以及清除过程的动力学。输出包括呼吸活性和[O(2)]从根中心到呼吸计介质的移动图像和数据文件。 • 任何位置的呼吸都遵循线粒体细胞色素氧化酶 O(2)依赖曲线(米氏常数 K(m) = 0.0108 kPa;临界 O(2)压力,1-2 kPa),O(2)消耗的下降速率被证明是两阶段的:最初是长的半线性部分,反映了严重缺氧在中柱内的扩散,随后是短的曲线下降,反映了它通过中皮层和皮层的延伸。 • 我们的结论是,最近在呼吸计研究中观察到的根呼吸初始呼吸下降归因于严重缺氧从中柱中心的扩散,而不是基于 O(2)传感器的呼吸受控下调来节约 O(2)。

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