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A Rice Plastidial Nucleotide Sugar Epimerase Is Involved in Galactolipid Biosynthesis and Improves Photosynthetic Efficiency

机译:水稻稻瘟病菌核苷酸糖差向异构酶参与半乳糖脂的生物合成并提高光合效率

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摘要

Photosynthesis is the final determinator for crop yield. To gain insight into genes controlling photosynthetic capacity, we selected from our large T-DNA mutant population a rice stunted growth mutant with decreased carbon assimilate and yield production named photoassimilate defective1 (phd1). Molecular and biochemical analyses revealed that PHD1 encodes a novel chloroplast-localized UDP-glucose epimerase (UGE), which is conserved in the plant kingdom. The chloroplast localization of PHD1 was confirmed by immunoblots, immunocytochemistry, and UGE activity in isolated chloroplasts, which was approximately 50% lower in the phd1-1 mutant than in the wild type. In addition, the amounts of UDP-glucose and UDP-galactose substrates in chloroplasts were significantly higher and lower, respectively, indicating that PHD1 was responsible for a major part of UGE activity in plastids. The relative amount of monogalactosyldiacylglycerol (MGDG), a major chloroplast membrane galactolipid, was decreased in the mutant, while the digalactosyldiacylglycerol (DGDG) amount was not significantly altered, suggesting that PHD1 participates mainly in UDP-galactose supply for MGDG biosynthesis in chloroplasts. The phd1 mutant showed decreased chlorophyll content, photosynthetic activity, and altered chloroplast ultrastructure, suggesting that a correct amount of galactoglycerolipids and the ratio of glycolipids versus phospholipids are necessary for proper chloroplast function. Downregulated expression of starch biosynthesis genes and upregulated expression of sucrose cleavage genes might be a result of reduced photosynthetic activity and account for the decreased starch and sucrose levels seen in phd1 leaves. PHD1 overexpression increased photosynthetic efficiency, biomass, and grain production, suggesting that PHD1 plays an important role in supplying sufficient galactolipids to thylakoid membranes for proper chloroplast biogenesis and photosynthetic activity. These findings will be useful for improving crop yields and for bioenergy crop engineering.
机译:光合作用是决定作物产量的最终决定因素。为了深入了解控制光合作用能力的基因,我们从我们的大型T-DNA突变体种群中选择了一个水稻发育不良的生长突变体,其碳同化物含量降低,产量提高,称为光同化缺陷1(phd1)。分子和生化分析表明,PHD1编码一种新的叶绿体定位的UDP-葡萄糖差向异构酶(UGE),在植物界中是保守的。通过免疫印迹,免疫细胞化学和分离的叶绿体中的UGE活性证实了PHD1的叶绿体定位,其在phd1-1突变体中比在野生型中低约50%。此外,叶绿体中UDP-葡萄糖和UDP-半乳糖底物的含量分别显着较高和较低,这表明PHD1负责质体中UGE活性的主要部分。在突变体中,主要叶绿体膜半乳糖脂的单半乳糖基二酰基甘油(MGDG)的相对数量减少,而二半乳糖基二酰基甘油(DGDG)的数量没有显着改变,这表明PHD1主要参与UDP-半乳糖供应,用于叶绿体中MGDG的生物合成。 phd1突变体显示出降低的叶绿素含量,光合活性和改变的叶绿体超微结构,表明正确数量的半乳甘油脂和糖脂与磷脂的比例对于适当的叶绿体功能是必需的。淀粉生物合成基因的表达下调和蔗糖裂解基因的表达上调可能是光合作用降低的结果,并解释了phd1叶片中淀粉和蔗糖水平的降低。 PHD1的过表达增加了光合作用的效率,生物量和谷物的产量,这表明PHD1在为类囊体膜提供足够的半乳糖脂以提供适当的叶绿体生物发生和光合作用方面起着重要作用。这些发现将有助于提高作物产量和生物能源作物工程。

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