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杜氏盐藻中甘油合成对渗透变化的响应调控

Regulation of glycerol synthesis in response to osmotic changes in dunaliella.

作者信息

Chitlaru E, Pick U

机构信息

Department of Biochemistry, The Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

Plant Physiol. 1991 May;96(1):50-60. doi: 10.1104/pp.96.1.50.

Abstract

Changes in phosphometabolites, following osmotic shock, were analyzed by two-dimensional thin layer chromatography, in extracts of the halotolerant alga Dunaliella salina in order to clarify the regulation of glycerol synthesis from starch. The experiments were carried out in wild-type and in osmotically defective mutant cells. It is demonstrated that hyperosmotic shock induces a decrease in fructose 6-phosphate and an increase in fructose-1,6-bisphosphate indicating the activation of phosphofructokinase. Two mutants, which are specifically defective in their response to hyperosmotic shock, accumulate glucose 6-phosphate or phosphogluconate following shock, and have remarkably reduced activities of glucose-6-phosphate dehydrogenase and of phosphogluconate dehydrogenase, respectively. These results indicate that the pentose-phosphate oxidative pathway has a major role in glycerol synthesis. Hyperosmotic shock leads to a transient accumulation of phosphorylcholine and to a decrease of inositolbisphosphate in D. salina extracts. Accumulation of phosphorylcholine is not detected in osmotically defective mutants. Hypoosmotic shock induces an increase in inositolbisphosphate but not in phosphorylcholine. These results are consistent with previous indications for differential activations of phospholipases by hyper or hypoosmotic shock in Dunaliella. Based on these results we suggest that (a) phosphofructokinase is an important checkpoint enzyme in the regulation of glycerol production, and (b) that the pentose-phosphate pathway has a major role in keeping oxidation-reduction balance during glycerol synthesis. The possible role of lipid breakdown products as second messengers in regulating glycerol production in Dunaliella is discussed.

摘要

为了阐明盐生杜氏藻中淀粉合成甘油的调控机制,采用二维薄层色谱法分析了渗透休克后耐盐藻杜氏盐藻提取物中磷酸代谢物的变化。实验在野生型和渗透缺陷型突变细胞中进行。结果表明,高渗休克诱导6-磷酸果糖减少,1,6-二磷酸果糖增加,表明磷酸果糖激酶被激活。两个对高渗休克反应存在特异性缺陷的突变体,在休克后分别积累6-磷酸葡萄糖或磷酸葡萄糖酸,且6-磷酸葡萄糖脱氢酶和磷酸葡萄糖酸脱氢酶的活性显著降低。这些结果表明戊糖磷酸氧化途径在甘油合成中起主要作用。高渗休克导致杜氏盐藻提取物中磷酸胆碱短暂积累,肌醇二磷酸减少。在渗透缺陷型突变体中未检测到磷酸胆碱的积累。低渗休克诱导肌醇二磷酸增加,但不诱导磷酸胆碱增加。这些结果与之前关于杜氏盐藻中高渗或低渗休克对磷脂酶的差异激活的研究结果一致。基于这些结果,我们认为:(a)磷酸果糖激酶是甘油生产调控中的一个重要检查点酶;(b)戊糖磷酸途径在甘油合成过程中维持氧化还原平衡方面起主要作用。还讨论了脂质分解产物作为第二信使在调控杜氏盐藻甘油生产中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5afa/1080712/00e7c861f626/plntphys00691-0061-a.jpg

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