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Updated: Aug 21, 2026

A β-glucuronidase (GUS) Based Cell Death Assay
Published on: May 6, 2011
Catalase and alternative oxidase cooperatively regulate programmed cell death induced by beta-glucan elicitor in
Masashi Mizuno1, Yasuomi Tada, Kimitaka Uchii
1Faculty of Agriculture, Kobe University, Nada-ku, Kobe 657-8501, Japan. mizuno@kobe-u.ac.jp
Abstract:
In potato (Solanum tuberosum L.) suspension cells, the expression of the gene encoding alternative oxidase (AOX) and H2O2 accumulation were induced by treatment with beta-glucan elicitor. The inhibition of catalase activity enhanced both AOX mRNA expression and the production of H2O2, whereas the ascorbate peroxidase inhibitor did not have any effect on these responses. Simultaneous inhibition of catalase and AOX activities in elicited cells dramatically increased H2O2 accumulation, leading to the disruption of mitochondrial membrane potential (deltapsi(m)) and programmed cell death (PCD). The results demonstrate, for the first time, that not only AOX but also catalase plays a central role in the suppression of mitochondrial deltapsi(m) breakdown and PCD induced by beta-glucan elicitor.
Insights
Potato cells treated with beta-glucan elicitor showed increased alternative oxidase (AOX) and hydrogen peroxide (H2O2). Catalase, alongside AOX, is crucial in preventing mitochondrial breakdown and programmed cell death (PCD).
Area of Science:
- Plant molecular biology
- Biochemistry
- Cellular stress responses
Background:
- Beta-glucan elicitors trigger defense responses in potato (Solanum tuberosum L.) cells.
- Alternative oxidase (AOX) and hydrogen peroxide (H2O2) are implicated in plant stress signaling.
Purpose of the Study:
- To investigate the roles of alternative oxidase (AOX) and catalase in beta-glucan-induced programmed cell death (PCD) in potato cells.
- To elucidate the involvement of H2O2 accumulation and mitochondrial membrane potential (deltapsi(m)) in these processes.
Main Methods:
- Potato suspension cells were treated with beta-glucan elicitor.
- Enzyme activities of catalase and ascorbate peroxidase were inhibited.
- AOX gene expression and H2O2 levels were measured.
- Mitochondrial membrane potential (deltapsi(m)) and PCD were assessed.
Main Results:
- Beta-glucan treatment induced AOX expression and H2O2 accumulation.
- Catalase inhibition enhanced AOX mRNA and H2O2 production, while ascorbate peroxidase inhibition had no effect.
- Simultaneous inhibition of catalase and AOX led to significant H2O2 increase, mitochondrial dysfunction, and PCD.
Conclusions:
- Catalase plays a critical role, alongside AOX, in suppressing beta-glucan-induced mitochondrial deltapsi(m) breakdown and PCD in potato cells.
- This study highlights a novel regulatory mechanism involving catalase in plant defense signaling and cell death pathways.
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