Noctor G., Strohm M., Jouanin L., Kunert K. J., Foyer C. H., Rennenberg H.
Laboratoire du Metabolisme (G.N.) and Laboratoire de Biologie Cellulaire (L.J.), Institut National de la Recherche Agronomique, Route de Saint-Cyr, 78026 Versailles Cedex, France.
Plant Physiol. 1996 Nov;112(3):1071-1078. doi: 10.1104/pp.112.3.1071.
Internode stem fragments of the poplar hybrid Populus tremula x Populus alba were transformed with a bacterial gene (gshl) for [gamma]-glutamylcysteine synthetase ([gamma]-ECS) targeted to the cytosol. Lines overexpressing [gamma]-ECS were identified by northern analysis, and the transformant with the highest enzyme activity was used to investigate the control of glutathione synthesis. Whereas foliar [gamma]-ECS activity was below the limit of detection in untransformed plants, activities of up to 8.7 nmol mg-1 protein min-1 were found in the transformant, in which the foliar contents of [gamma]-glutamylcysteine ([gamma]-EC) and glutathione were increased approximately 10- and 3-fold, respectively, without affecting either the reduction state of the glutathione pool or the foliar cysteine content. A supply of exogenous cysteine to leaf discs increased the glutathione content from both transformed and untransformed poplars, and caused the [gamma]-EC content of the transformant discs to increase still further. The following conclusions are drawn: (a) the native [gamma]-ECS of untransformed poplars exists in quantities that are limiting for foliar glutathione synthesis; (b) foliar glutathione synthesis in untransformed poplars is limited by cysteine availability; (c) in the transformant interactions between glutathione synthesis and cysteine synthesis operate to sustain the increased formation of [gamma]-EC and glutathione; and (d) the foliar glutathione content of the transformant is restricted by cysteine availability and by the activity of glutathione synthetase.
将白杨杂种欧洲山杨×银白杨的节间茎段用靶向细胞质的细菌γ-谷氨酰半胱氨酸合成酶(γ-ECS)基因(gshl)进行转化。通过Northern分析鉴定出γ-ECS过表达的株系,并使用酶活性最高的转化体来研究谷胱甘肽合成的调控。在未转化的植株中,叶片γ-ECS活性低于检测限,而在转化体中发现其活性高达8.7 nmol mg-1蛋白min-1,其中γ-谷氨酰半胱氨酸(γ-EC)和谷胱甘肽的叶片含量分别增加了约10倍和3倍,而不影响谷胱甘肽库的还原状态或叶片半胱氨酸含量。向叶盘供应外源半胱氨酸增加了转化和未转化杨树的谷胱甘肽含量,并使转化体叶盘的γ-EC含量进一步增加。得出以下结论:(a)未转化杨树的天然γ-ECS数量限制了叶片谷胱甘肽的合成;(b)未转化杨树的叶片谷胱甘肽合成受半胱氨酸可用性的限制;(c)在转化体中,谷胱甘肽合成与半胱氨酸合成之间的相互作用维持了γ-EC和谷胱甘肽形成的增加;(d)转化体的叶片谷胱甘肽含量受半胱氨酸可用性和谷胱甘肽合成酶活性的限制。