Figure 5.
ETR (I) with or without DBMIB showed CYP37 potential functions in transferring electrons. A) No difference was observed in the ETR (I) of WT and cyp37-1 grown under GL conditions (90 μmol·m−2·s−1) with or without 10 μM DBMIB treatment. WT and cyp37-1 plants were grown under GL for 5 wk, then detached leaves were treated with mock or 10 μM DBMIB in the dark for 2 h and then used for ETR (I) determination. Data represent the means ± Sd, n = 3. PPFD, photosynthetic photon flux density. B) NBT staining showed that superoxide radical accumulation was the same as WT in cyp37-1 mutant plants under GL conditions with or without 10 μM DBMIB treatment. Scale bars: 0.5 cm. C)cyp37-1 mutant showed a similar level of ETR (I) as that observed in WT plants treated with 10 μM DBMIB under HL conditions (350 μmol·m−2·s−1). WT and cyp37-1 plants were grown in GL conditions for 5 wk and then exposed to HL conditions for 4 d. The leaves were treated with mock or 10 μM DBMIB in the dark for 2 h and then used for ETR determination. Data represent the means ± Sd, n = 3. D) The cyp37-1 mutant showed a similar level of ROS accumulation as that observed in WT plants treated with 10 μM DBMIB under HL stress conditions.

ETR (I) with or without DBMIB showed CYP37 potential functions in transferring electrons. A) No difference was observed in the ETR (I) of WT and cyp37-1 grown under GL conditions (90 μmol·m−2·s−1) with or without 10 μM DBMIB treatment. WT and cyp37-1 plants were grown under GL for 5 wk, then detached leaves were treated with mock or 10 μM DBMIB in the dark for 2 h and then used for ETR (I) determination. Data represent the means ± Sd, n = 3. PPFD, photosynthetic photon flux density. B) NBT staining showed that superoxide radical accumulation was the same as WT in cyp37-1 mutant plants under GL conditions with or without 10 μM DBMIB treatment. Scale bars: 0.5 cm. C)cyp37-1 mutant showed a similar level of ETR (I) as that observed in WT plants treated with 10 μM DBMIB under HL conditions (350 μmol·m−2·s−1). WT and cyp37-1 plants were grown in GL conditions for 5 wk and then exposed to HL conditions for 4 d. The leaves were treated with mock or 10 μM DBMIB in the dark for 2 h and then used for ETR determination. Data represent the means ± Sd, n = 3. D) The cyp37-1 mutant showed a similar level of ROS accumulation as that observed in WT plants treated with 10 μM DBMIB under HL stress conditions.

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