首页> 外文期刊>Plant, Cell & Environment >Regulation of cyclic electron flow in C-3 plants: differential effects of limiting photosynthesis at ribulose-1,5-bisphosphate carboxylase/oxygenase and glyceraldehyde-3-phosphate dehydrogenase
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Regulation of cyclic electron flow in C-3 plants: differential effects of limiting photosynthesis at ribulose-1,5-bisphosphate carboxylase/oxygenase and glyceraldehyde-3-phosphate dehydrogenase

机译:C-3植物中循环电子流的调节:限制光合作用对核糖-1,5-双磷酸羧化酶/加氧酶和甘油醛-3-磷酸脱氢酶的不同影响

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摘要

Cyclic electron flow around photosystem I (CEF1) is thought to augment chloroplast ATP production to meet metabolic needs. Very little is known about the induction and regulation of CEF1. We investigated the effects on CEF1 of antisense suppression of the Calvin-Benson enzymes glyceraldehyde-3-phosphate dehydrogenase (gapR), and ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) small subunit (SSU), in tobacco (Nicotiana tabacum cv. Wisconsin 38). The gapR, but not ssuR, mutants showed substantial increases in CEF1, demonstrating that specific intermediates, rather than slowing of assimilation, induce CEF1. Both types of mutant showed increases in steady-state transthylakoid proton motive force (pmf) and subsequent activation of the photoprotective q(E) response. With gapR, the increased pmf was caused both by up-regulation of CEF1 and down-regulation of the ATP synthase. In ssuR, the increased pmf was attributed entirely to a decrease in ATP synthase activity, as previously seen in wild-type plants when CO2 levels were decreased. Comparison of major stromal metabolites in gapR, ssuR and hcef1, a mutant with decreased fructose 1,6-bisphosphatase activity, showed that neither the ATP/ADP ratio, nor major Calvin-Benson cycle intermediates can directly account for the activation of CEF1, suggesting that chloroplast redox status or reactive oxygen species regulate CEF1.
机译:围绕光系统I(CEF1)的循环电子流被认为可以增加叶绿体ATP的产量,以满足代谢需要。关于CEF1的诱导和调控了解甚少。我们调查了对烟草中的Calvin-Benson酶甘油醛-3-磷酸脱氢酶(gapR)和核糖1,5-双磷酸羧化酶/加氧酶(Rubisco)小亚基(SSU)的反义抑制作用对CEF1的影响。 cv。Wisconsin 38)。 gapR突变体而不是ssuR突变体显示CEF1显着增加,表明特定的中间体(而不是减缓同化作用)诱导CEF1。两种类型的突变体均显示稳态跨类囊体质子动力(pmf)的增加以及随后的光保护性q(E)响应的激活。使用gapR,pmf的增加是由CEF1的上调和ATP合酶的下调引起的。在ssuR中,pmf的增加完全归因于ATP合酶活性的降低,如先前在野生型植物中观察到的,当CO2水平降低时。比较gapR,ssuR和hcef1中主要的基质代谢物(果糖1,6-双磷酸酶活性降低的突变体)表明,ATP / ADP比率或主要的Calvin-Benson循环中间体均不能直接说明CEF1的激活。叶绿体氧化还原状态或活性氧调节CEF1。

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