Memon A R, Boss W F
Department of Biological Sciences, Middle East Technical University, Ankara, Turkey.
J Biol Chem. 1990 Sep 5;265(25):14817-21.
Irradiation of sunflower (Helianthus annuus L. cv. Russian Mammoth) hypocotyls with white light resulted in a 51% decrease in plasma membrane phosphatidylinositol monophosphate (PIP) kinase activity. As little as 10 s of white light irradiation was sufficient to lower the phosphatidylinositol bisphosphate (PIP2) produced in the in vitro phosphorylation assay. This decrease was not caused by an increase in phospholipase C activity since analysis of the water-soluble products indicated no increase in inositol bisphosphate or inositol trisphosphate. Treatment of the plasma membrane with 200 microM vanadate prior to phosphorylation enhanced the PIP kinase and appeared to overcome the light inhibition. In addition to decreasing the PIP kinase activity, light irradiation resulted in a corresponding decrease in the H(+)-ATPase activity to 53% of the dark control values. The plasma membrane ATPase activity increased approximately 2-fold when PIP or PIP2 was added to the isolated membranes. Thus, effects of external stimuli on the level of plasma membrane PIP or PIP2 could affect plasma membrane ATPase activity directly and thereby provide an alternative mechanism for control of cell growth.
用白光照射向日葵(向日葵属俄罗斯猛犸象品种)下胚轴,导致质膜磷脂酰肌醇单磷酸(PIP)激酶活性降低51%。仅10秒的白光照射就足以降低体外磷酸化试验中产生的磷脂酰肌醇二磷酸(PIP2)。这种降低不是由磷脂酶C活性增加引起的,因为对水溶性产物的分析表明肌醇二磷酸或肌醇三磷酸没有增加。在磷酸化之前用200微摩尔钒酸盐处理质膜可增强PIP激酶活性,并且似乎能克服光抑制作用。除了降低PIP激酶活性外,光照还导致H(+) - ATP酶活性相应降低至黑暗对照值的53%。当将PIP或PIP2添加到分离的膜中时,质膜ATP酶活性增加约2倍。因此,外部刺激对质膜PIP或PIP2水平的影响可能直接影响质膜ATP酶活性,从而为控制细胞生长提供一种替代机制。