Abstract
We studied the signal transduction system of cytosolic ascorbate peroxidase (APX) in spinach. When the detached spinach leaves were treated with 3-aminotriazol and methyl viologen, the cellular H2O2 levels and the transcript level of cytosolic APX (cAPX) were increased. The H2O2 treatment also increased the transcript level of cAPX.
The treatment of DCMU inhibited the induction of cAPX transcript level under high light intensity. In contrast, the treatment with DBMIB increased the transcript level of cAPX under low light intensity. These results indicate that cAPX is regulated by the redox status of plastquinone pool or cellular H2O2 level. Currently, we are analyzing the effects of the production of H2O2 and the over-reduction of plastquinone pool on cAPX induction under high light intensity using transgenic tobacco plants expressing the E. coli catalase (T43-1) or thylakoid-membrane bound APX (TpTAP-12) in chloroplasts.