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ABSTRACT: Background
Mitochondria are the center of energy metabolism and the production of reactive oxygen species (ROS). ROS production results in a burst of "superoxide flashes", which is always accompanied by depolarization of mitochondrial membrane potential. Superoxide flashes have only been studied in the model plant Arabidopsis thaliana using a complex method to isolate mitochondria. In this study, we present an efficient, easier method to isolate functional mitochondria from floral tissues to measure superoxide flashes.Method
We used 0.5 g samples to isolate mitochondria within <1.5 h from flowers of two non-transgenic plants (Magnolia denudata and Nelumbo nucifera) to measure superoxide flashes. Superoxide flashes were visualized by the pH-insensitive indicator MitoSOX Red, while the mitochondrial membrane potential (?? m) was labelled with TMRM.Results
Mitochondria isolated using our method showed a high respiration ratio. Our results indicate that the location of ROS and mitochondria was in a good coincidence. Increased ROS together with a higher frequency of superoxide flashes was found in mitochondria isolated from the flower pistil. Furthermore, a higher rate of depolarization of the ?? m was observed in the pistil. Taken together, these results demonstrate that the frequency of superoxide flashes is closely related to depolarization of the ?? m in petals and pistils of flowers.
SUBMITTER: Zhang C
PROVIDER: S-EPMC6462395 | biostudies-literature | 2019
REPOSITORIES: biostudies-literature
Zhang Chulan C Sun Fengshuo F Xiong Biao B Zhang Zhixiang Z
PeerJ 20190411
<h4>Background</h4>Mitochondria are the center of energy metabolism and the production of reactive oxygen species (ROS). ROS production results in a burst of "superoxide flashes", which is always accompanied by depolarization of mitochondrial membrane potential. Superoxide flashes have only been studied in the model plant <i>Arabidopsis thaliana</i> using a complex method to isolate mitochondria. In this study, we present an efficient, easier method to isolate functional mitochondria from floral ...[more]