The Key Targets of NO-Mediated Post-Translation Modification (PTM) Highlighting the Dynamic Metabolism of ROS and RNS in Peroxisomes

被引:4
作者
Ergashev, Ulugbek [1 ]
Yu, Mei [1 ]
Luo, Long [1 ]
Tang, Jie [2 ]
Han, Yi [1 ]
机构
[1] Anhui Agr Univ, Sch Life Sci, Natl Engn Lab Crop Stress Resistance Breeding, Hefei 230036, Peoples R China
[2] Anhui Agr Univ, Sch Resources & Environm, Anhui Prov Key Lab Hazardous Factors & Risk Contro, Hefei 230036, Peoples R China
关键词
nitric oxide (NO); reactive nitrogen species (RNS); S-nitrosoglutathione (GSNO); peroxynitrite; (ONOO-); post-translational modification (PTM); H2O2; PROTEIN S-NITROSYLATION; NITRIC-OXIDE; TYROSINE NITRATION; MONODEHYDROASCORBATE REDUCTASE; GLUTATHIONE-REDUCTASE; ABIOTIC STRESS; BIOTIN SWITCH; IDENTIFICATION; NITROSOGLUTATHIONE; TRANSNITROSYLATION;
D O I
10.3390/ijms25168873
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nitric oxide (NO) has been firmly established as a key signaling molecule in plants, playing a significant role in regulating growth, development and stress responses. Given the imperative of sustainable agriculture and the urgent need to meet the escalating global demand for food, it is imperative to safeguard crop plants from the effects of climate fluctuations. Plants respond to environmental challenges by producing redox molecules, including reactive oxygen species (ROS) and reactive nitrogen species (RNS), which regulate cellular, physiological, and molecular processes. Nitric oxide (NO) plays a crucial role in plant stress tolerance, acting as a signaling molecule or free radical. NO is involved in various developmental processes in plants through diverse mechanisms. Exogenous NO supplementation can alleviate the toxicity of abiotic stresses and enhance plant resistance. In this review we summarize the studies regarding the production of NO in peroxisomes, and how its molecule and its derived products, (ONOO-) and S-nitrosoglutathione (GSNO) affect ROS metabolism in peroxisomes. Peroxisomal antioxidant enzymes including catalase (CAT), are key targets of NO-mediated post-translational modification (PTM) highlighting the dynamic metabolism of ROS and RNS in peroxisomes.
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页数:16
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