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首页> 外文期刊>Plant physiology >NADP-malate dehydrogenase in the C4 plant Flaveria bidentis. Cosense suppression of activity in mesophyll and bundle-sheath cells and consequences for photosynthesis.
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NADP-malate dehydrogenase in the C4 plant Flaveria bidentis. Cosense suppression of activity in mesophyll and bundle-sheath cells and consequences for photosynthesis.

机译:C4植物黄萎病中的NADP-苹果酸脱氢酶。共同抑制叶肉和束鞘细胞中的活性以及对光合作用的影响。

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摘要

Flaveria bidentis, a C4 dicot, was transformed with sorghum (a monocot) cDNA clones encoding NADP-malate dehydrogenase (NADP-MDH; EC 1.1.1.82) driven by the cauliflower mosaic virus 35S promoter. Although these constructs were designed for over-expression, many transformants contained between 5 and 50% of normal NADP-MDH activity, presumably by cosense suppression of the native gene. The activities of a range of other photosynthetic enzymes were unaffected. Rates of photosynthesis in plants with less than about 10% of normal activity were reduced at high light and at high CO2 concentrations, but were unaffected at low light or at CO2 concentrations below about 150 鎙 litre-1. The large decrease in maximum activity of NADP-MDH was accompanied by anincrease in the activation state of the enzyme. However, the activation state was unaffected in plants with 50% of normal activity. Metabolic flux control analysis of plants with a range of activities demonstrated that this enzyme is not important in regulating the steady-state flux through C4 photosynthesis in F. bidentis. Cosense suppression of gene expression was similarly effective in both the mesophyll and bundle-sheath cells. Photosynthesis of plants with very low activity of NADP-MDH in the bundle-sheath cells was only slightly inhibited, suggesting that the presence of the enzyme in this compartment is not essential for supporting maximum rates of photosynthesis.
机译:用高粱(单子叶植物)转化高粱(单子叶植物)黄花牛cDNA克隆,该cDNA克隆由花椰菜花叶病毒35S启动子驱动,编码NADP-苹果酸脱氢酶(NADP-MDH; EC 1.1.1.82)。尽管这些构建体是为过表达而设计的,但许多转化体可能包含正常NADP-MDH活性的5%至50%,大概是由于天然基因的共义抑制。一系列其他光合酶的活性不受影响。在高光照和高CO2浓度下,正常活性低于10%的植物的光合作用速率会降低,但在低光照或CO2浓度低于150升-1时,光合作用的速率不会受到影响。 NADP-MDH的最大活性大大降低,同时伴随着酶激活状态的增加。但是,激活状态在正常活性为50%的植物中不受影响。对具有多种活性的植物进行的代谢通量控制分析表明,该酶在通过双歧F的C4光合作用调节稳态通量中并不重要。共同抑制基因表达在叶肉和束鞘细胞中同样有效。束鞘细胞中NADP-MDH活性极低的植物的光合作用仅受到轻微抑制,这表明该隔室中酶的存在对于支持最大的光合作用率不是必不可少的。

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