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在硫饥饿条件下一种硫脂的合成和降解的调节及其在莱茵衣藻中的生理意义。

Regulation of synthesis and degradation of a sulfolipid under sulfur-starved conditions and its physiological significance in Chlamydomonas reinhardtii.

机构信息

School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Horinouchi, Hachioji, Tokyo 192-0392, Japan.

出版信息

New Phytol. 2010 Feb;185(3):676-86. doi: 10.1111/j.1469-8137.2009.03115.x. Epub 2009 Dec 14.

Abstract

Regulation of synthesis and degradation of sulfoquinovosyl diacylglycerol (SQDG), one of the membrane lipids that construct thylakoids, under sulfur (S)-starved conditions and its physiological significance were explored in a green alga, Chlamydomonas reinhardtii. Here, we used sac1 and sac3 mutants defective in response to ambient S-status to characterize the system of known induction of SQDG degradation by S starvation that ensures a major S source for protein synthesis. The SQDG synthesis system was monitored in the wild type during S starvation. An SQDG-deficient mutant, hf-2, was utilized to discover functions where SQDG metabolism participates during S starvation. The induction of SQDG degradation was largely repressed in both sac1 and sac3 mutants. The SQDG synthesis capacity was increased by 40% after S starvation, with a sixfold elevation in the mRNA level of the SQD1 gene for SQDG synthesis. Compared with the wild type, hf-2 had decreased protein accumulation, photosystem (PS) I stability and growth rate. A role of SQDG as an S storage lipid is fulfilled under the control of both SAC1 and SAC3 genes, and it is essential for proper protein synthesis in acclimatization of cells to S starvation. The enhancement in SQDG synthesis may reflect the importance of SQDG as the membrane lipid that stabilizes the PSI complex.

摘要

在绿藻衣藻中探索了硫饥饿条件下构建类囊体膜脂磺基奎诺糖二酰甘油(SQDG)的合成和降解的调控及其生理意义。在这里,我们使用对环境 S 状态无反应的 sac1 和 sac3 突变体来表征已知的由 S 饥饿诱导 SQDG 降解的系统,该系统确保了蛋白质合成的主要 S 来源。在 S 饥饿期间,监测野生型中的 SQDG 合成系统。利用 SQDG 缺陷突变体 hf-2 来发现 SQDG 代谢在 S 饥饿期间参与的功能。在 sac1 和 sac3 突变体中,SQDG 降解的诱导被大大抑制。S 饥饿后 SQDG 合成能力增加了 40%,SQDG 合成的 SQD1 基因的 mRNA 水平升高了六倍。与野生型相比,hf-2 的蛋白积累、PS I 稳定性和生长速率降低。在 SAC1 和 SAC3 基因的控制下,SQDG 作为一种 S 储存脂质发挥作用,对于细胞适应 S 饥饿时的适当蛋白质合成是必不可少的。SQDG 合成的增强可能反映了 SQDG 作为稳定 PSI 复合物的膜脂的重要性。

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