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Transgenic Tobacco Plants Overexpressing Chloroplastic Ferredoxin-NADP(H) Reductase Display Normal Rates of Photosynthesis and Increased Tolerance to Oxidative Stress1

机译:过表达叶绿体铁氧还蛋白-NADP(H)还原酶的转基因烟草植物显示出正常的光合作用速率和对氧化胁迫的耐受性1

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摘要

Ferredoxin-NADP(H) reductase (FNR) catalyzes the last step of photosynthetic electron transport in chloroplasts, driving electrons from reduced ferredoxin to NADP+. This reaction is rate limiting for photosynthesis under a wide range of illumination conditions, as revealed by analysis of plants transformed with an antisense version of the FNR gene. To investigate whether accumulation of this flavoprotein over wild-type levels could improve photosynthetic efficiency and growth, we generated transgenic tobacco (Nicotiana tabacum) plants expressing a pea (Pisum sativum) FNR targeted to chloroplasts. The alien product distributed between the thylakoid membranes and the chloroplast stroma. Transformants grown at 150 or 700 μmol quanta m−2 s−1 displayed wild-type phenotypes regardless of FNR content. Thylakoids isolated from plants with a 5-fold FNR increase over the wild type displayed only moderate stimulation (approximately 20%) in the rates of electron transport from water to NADP+. In contrast, when donors of photosystem I were used to drive NADP+ photoreduction, the activity was 3- to 4-fold higher than the wild-type controls. Plants expressing various levels of FNR (from 1- to 3.6-fold over the wild type) failed to show significant differences in CO2 assimilation rates when assayed over a range of light intensities and CO2 concentrations. Transgenic lines exhibited enhanced tolerance to photooxidative damage and redox-cycling herbicides that propagate reactive oxygen species. The results suggest that photosynthetic electron transport has several rate-limiting steps, with FNR catalyzing just one of them.
机译:铁氧还蛋白-NADP(H)还原酶(FNR)催化了叶绿体中光合电子传输的最后一步,将电子从还原的铁氧还蛋白驱动到NADP +。如通过分析用反义形式的FNR基因转化的植物所揭示的,该反应是在宽范围的光照条件下光合作用的速率限制。为了调查这种黄素蛋白在野生型水平上的积累是否可以提高光合效率和生长,我们生成了表达针对叶绿体的豌豆(Pisum sativum)FNR的转基因烟草(Nicotiana tabacum)植物。外来产物分布在类囊体膜和叶绿体基质之间。无论FNR含量如何,在150或700μmol量子m-2 s-1处生长的转化子均显示野生型表型。从植物中分离的类囊体的FNR比野生型增加了5倍,从水到NADP +的电子传输速率仅表现出中等程度的刺激(约20%)。相反,当使用光系统I的供体驱动NADP +光还原时,其活性比野生型对照高3至​​4倍。在各种光强度和CO2浓度范围内进行分析时,表达各种水平FNR(比野生型高1到3.6倍)的植物在CO2同化率上均未显示出显着差异。转基因品系对光氧化损伤和传播活性氧的氧化还原循环除草剂表现出更高的耐受性。结果表明,光合电子传递具有多个限速步骤,其中FNR催化其中之一。

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