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赤霉素对燕麦茎段中葡萄糖代谢和细胞壁合成的调节作用。

Regulation of glucose metabolism and cell wall synthesis in Avena stem segments by gibberellic Acid.

机构信息

Department of Cellular and Molecular Biology, Division of Biological Sciences, University of Michigan, Ann Arbor, Michigan 48109.

出版信息

Plant Physiol. 1978 Sep;62(3):391-6. doi: 10.1104/pp.62.3.391.

Abstract

Gibberellic acid (GA) stimulated both the elongation of Avena sativa stem segments and increased synthesis of cell wall material. The effects of GA on glucose metabolism, as related to cell wall synthesis, have been investigated in order to find specific events regulated by GA. GA caused a decline in the levels of glucose, glucose 6-phosphate, and fructose 6-phosphate if exogenous sugar was not supplied to the segments, whereas the hormone caused no change in the levels of glucose 6-phosphate, fructose 6-phosphate, UDP-glucose, or the adenylate energy charge if the segments were incubated in 0.1 m glucose. No GA-induced change could be demonstrated in the activities of hexokinase, phosphoglucomutase, UDP-glucose pyrophosphorylase, or polysaccharide synthetases using UDP-glucose, UDP-galactose, UDP-xylose, and UDP-arabinose as substrates. GA stimulated the activity of GDP-glucose-dependent beta-glucan synthetase by 2- to 4-fold over the control. When glucan synthetase was assayed using UDP-glucose as substrate, only beta-1,3-linked glucan was synthesized in vitro, whereas with GDP-glucose, only beta-1,4-linked glucan was synthesized. These results suggest that one part of the mechanism by which GA stimulates cell wall synthesis concurrently with elongation in Avena stem segments may be through a stimulation of cell wall polysaccharide synthetase activity.

摘要

赤霉素(GA)既能刺激燕麦茎切段的伸长,又能促进细胞壁物质的合成。为了找到受 GA 调控的特定事件,我们研究了 GA 对与细胞壁合成有关的葡萄糖代谢的影响。如果不给切段提供外源糖,GA 会导致葡萄糖、葡萄糖 6-磷酸和果糖 6-磷酸的水平下降,而如果在 0.1 m 葡萄糖中孵育,激素不会改变葡萄糖 6-磷酸、果糖 6-磷酸、UDP-葡萄糖或腺苷酸能量电荷的水平。如果以 UDP-葡萄糖、UDP-半乳糖、UDP-木糖和 UDP-阿拉伯糖为底物,使用 hexokinase、phosphoglucomutase、UDP-glucose pyrophosphorylase 或多糖合成酶,都无法证明 GA 诱导的活性变化。GA 刺激 GDP-葡萄糖依赖性β-葡聚糖合成酶的活性比对照增加 2 到 4 倍。当使用 UDP-葡萄糖作为底物测定葡聚糖合酶时,仅在体外合成β-1,3 连接的葡聚糖,而使用 GDP-葡萄糖时,仅合成β-1,4 连接的葡聚糖。这些结果表明,GA 刺激燕麦茎切段伸长和细胞壁合成的机制之一可能是通过刺激细胞壁多糖合成酶的活性。

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