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. 2014 Jan 7;9:e27389. doi: 10.4161/psb.27389

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Figure 1. Response of OsSUV3 transgenic plants to heavy metal stress. Quantitative real-time PCR analysis of OsSUV3 under different abiotic stress conditions (A) 200 µM CdCl2 (B) 300 µM ZnCl2. Total RNA isolation was done from leaf samples collected at different time intervals (viz. One h, 2 h, 3 h, 6 h, 12 h). Bars indicate the standard error (± SE) calculated from three independent experiments. (C) Leaf disk senescence assay of OsSUV3 transgenic rice plants along with antisense (AS), vector control (VC) and wild-type (WT) in presence of 200 µM CdCl2 and 300 µM ZnCl2. (D) Estimation of total chlorophyll content of OsSUV3 transgenic plants along with AS, VC and WT plants after CdCl2 stress. (E) Estimation of total chlorophyll content of OsSUV3 transgenic plants after ZnCl2 stress. (F) Germination test of T2 SUV3 transgenic AS, VC and WT seeds in MS plate supplemented with 200 µM CdCl2. (G) Germination of T2 SUV3 transgenic seeds after 300 µM ZnCl2. (H) Fresh weight per 10 seedlings from MS plate supplemented with 200 µM CdCl2. (I) Fresh weight per 10 seedlings from MS plate supplemented with 300 µM ZnCl2.