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高光在黄瓜(Cucumis sativus)子叶脱黄化过程中,在5-氨基乙酰丙酸合成水平上抑制叶绿素生物合成。

High light inhibits chlorophyll biosynthesis at the level of 5-aminolevulinate synthesis during de-etiolation in cucumber (Cucumis sativus) cotyledons.

作者信息

Aarti D, Tanaka R, Ito H, Tanaka A

机构信息

Institute of Low Temperature Science, Hokkaido University, Sapporo, Japan.

出版信息

Photochem Photobiol. 2007 Jan-Feb;83(1):171-6. doi: 10.1562/2006-03-06-RA-835.

Abstract

Using the vascular plant Cucumis sativus (cucumber) as a model, we studied the effects of high (intense and excess) light upon chlorophyll biosynthesis during de-etiolation. When illuminated with high light (1500-1600 microE/m2/s), etiolated cucumber cotyledons failed to synthesize chlorophyll entirely. However, upon transfer to low light conditions (40-45 microE/m2/s), chlorophyll biosynthesis and subsequent accumulation resumed following an initial 2-12 h delay. Duration of high light treatment negatively correlated with chlorophyll biosynthetic activity. Specifically, we found that high light severely inhibited 5-aminolevulinic acid (ALA) synthesis. This effect partly could be because of the decrease in protein level of glutamyl-tRNA reductase (GluTR) observed. Protein level of glutamate-1-semialdehyde (GSA-AT) remained unchanged. It was also found that high light did not suppress HEMA 1 expression. Therefore, we speculated that this significant inhibition of ALA synthesis might have occurred mainly because of concomitant inactivation of GluTR and/or inhibition of complex formation between GluTR and GSA-AT. Our further observation that both methyl viologen and rose bengal similarly inhibit ALA synthesis under low light conditions suggested that reactive oxygen species (ROS) could be responsible for the inhibition of ALA synthesis in cotyledons exposed to high light conditions.

摘要

以维管植物黄瓜为模型,我们研究了高光(强光和过量光)对脱黄化过程中叶绿素生物合成的影响。用高光(1500 - 1600微爱因斯坦/平方米/秒)照射时,黄化的黄瓜子叶完全无法合成叶绿素。然而,转移到低光条件(40 - 45微爱因斯坦/平方米/秒)后,叶绿素生物合成及随后的积累在最初延迟2 - 12小时后恢复。高光处理的持续时间与叶绿素生物合成活性呈负相关。具体而言,我们发现高光严重抑制5-氨基乙酰丙酸(ALA)的合成。这种效应部分可能是由于观察到的谷氨酰-tRNA还原酶(GluTR)蛋白水平下降。谷氨酸-1-半醛(GSA-AT)的蛋白水平保持不变。还发现高光并未抑制HEMA 1的表达。因此,我们推测ALA合成的这种显著抑制可能主要是由于GluTR的伴随失活和/或GluTR与GSA-AT之间复合物形成的抑制。我们进一步观察到,甲基紫精和孟加拉玫瑰红在低光条件下同样抑制ALA合成,这表明活性氧(ROS)可能是导致暴露于高光条件下子叶中ALA合成受抑制的原因。

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