Hieber A David, Kawabata Osamu, Yamamoto Harry Y
Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI 96822, USA.
Plant Cell Physiol. 2004 Jan;45(1):92-102. doi: 10.1093/pcp/pch010.
The dynamics of the xanthophyll cycle relative to non-photochemical quenching (NPQ) were examined in tobacco plants overexpressing violaxanthin de-epoxidase (VDE), PsbS and PsbS+VDE for effects on NPQ and violaxanthin (V) de-epoxidation over a range of light intensities. Induction of de-epoxidation and NPQ increased in overexpressed VDE and PsbS plants, respectively. Surprisingly, under low light, overexpressing PsbS enhanced de-epoxidation in addition to NPQ. The effect was hypothesized as due to PsbS binding zeaxanthin (Z) or inducing the binding of Z within the quenching complex, thus shifting the equilibrium toward higher de-epoxidation states. Studies in model systems show that Z can stereospecifically inhibit VDE activity against violaxanthin. This effect, observed under conditions of limiting lipid concentration, was interpreted as product feedback inhibition. These results support the hypothesis that the capacity of the thylakoid lipid phase for xanthophylls is limited and modulates xanthophyll-cycle activity, in conjunction with the release of V and binding of Z by pigment-binding proteins. These modulating factors are incorporated into a lipid-matrix model that has elements of a signal transduction system wherein the light-generated protons are the signal, VDE the signal receptor, Z the secondary messenger, the lipid phase the transduction network, and Z-binding proteins the targets.
在一系列光照强度下,研究了过表达紫黄质脱环氧化酶(VDE)、PsbS和PsbS + VDE的烟草植株中叶黄素循环相对于非光化学猝灭(NPQ)的动力学,以考察其对NPQ和紫黄质(V)脱环氧化的影响。过表达VDE和PsbS的植株中,脱环氧化和NPQ的诱导分别增加。令人惊讶的是,在低光照条件下,过表达PsbS除了增强NPQ外,还增强了脱环氧化。推测这种效应是由于PsbS结合玉米黄质(Z)或诱导Z在猝灭复合物中的结合,从而使平衡向更高的脱环氧化状态移动。模型系统研究表明,Z可以立体特异性地抑制VDE对紫黄质的活性。在脂质浓度受限的条件下观察到的这种效应被解释为产物反馈抑制。这些结果支持了这样的假设,即类囊体脂质相中叶黄素的容量是有限的,并与色素结合蛋白对V的释放和Z的结合一起调节叶黄素循环活性。这些调节因子被纳入一个脂质基质模型,该模型具有信号转导系统的元素,其中光产生的质子是信号,VDE是信号受体,Z是第二信使,脂质相是转导网络,Z结合蛋白是靶标。