Polyamine, 1,3-diaminopropane, regulates defence responses on growth, gas exchange, PSII photochemistry and antioxidant system in wheat under arsenic toxicity

Copyright © 2023 Elsevier Masson SAS. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Plant physiology and biochemistry : PPB. - 1991. - 201(2023) vom: 15. Aug., Seite 107886
1. Verfasser: Gulenturk, Cagri (VerfasserIn)
Weitere Verfasser: Alp-Turgut, Fatma Nur, Arikan, Busra, Tofan, Aysenur, Ozfidan-Konakci, Ceyda, Yildiztugay, Evren
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Plant physiology and biochemistry : PPB
Schlagworte:Journal Article 1,3-Diaminopropane Antioxidant Arsenic PSII photochemistry Triticum aestivum Antioxidants N712M78A8G Polyamines Thiobarbituric Acid Reactive Substances mehr... Hydrogen Peroxide BBX060AN9V trimethylenediamine CB3ISL56KG Ascorbic Acid PQ6CK8PD0R Glutathione GAN16C9B8O Peroxidase EC 1.11.1.7 Glutathione Peroxidase EC 1.11.1.9 Chlorophyll 1406-65-1
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520 |a The metalloid arsenic (As) is extremely hazardous to all living organisms, including plants. Pollution with As is very detrimental to the photosynthetic machinery, cell division, energy generation, and redox status. In order to cope with stress, the use of growth regulators such as polyamines (PA), which strengthen the antioxidant system of plants, has become widespread in recent years. PAs can modulate the plant growth through basic mechanisms common to all living organisms, such as membrane stabilization, free radical scavenging, deoxyribonucleic acid (DNA), ribonucleic acid (RNA) and protein synthesis, enzyme activities and second messengers. However, the effect of 1,3- diaminopropane (Dap), which is a product of PA catabolism, is not clear enough in plants exposed to As toxicity. In the current study, the different concentrations of 1,3-diaminopropane (0.1, 0.5 and 1 mM Dap) were hydroponically treated to wheat (Triticum aestivum) under arsenic stress (100 μM As) and then relative growth rate (RGR), relative water content (RWC), proline content (Pro), gas exchange parameters, PSII photochemistry, chlorophyll fluorescence kinetics, antioxidant activity and lipid peroxidation were assessed. RGR, RWC, osmotic potential and Pro content decreased in As-applied plants. The inhibition of these parameters could be reversed by Dap treatments. Besides, Dap applications mitigated the As toxicity-induced suppression on chlorophyll fluorescence (Fv/Fm, Fv/Fo and Fo/Fm) and the performance of PSII photochemistry. As impaired the balance on antioxidant capacity by decreased activities of catalase (CAT), peroxidase (POX), glutathione peroxidase (GPX), ascorbate peroxidase (APX), monodehydroascorbate reductase (MDHAR), dehydroascorbate reductase (DHAR), and the contents of ascorbate (AsA) and glutathione (GSH) and then lipid peroxidation (TBARS content) increased. In the presence of Dap under As stress, the plants exhibited an increase in superoxide dismutase (SOD), POX, and GPX. Dap treatments contributed to the maintenance of cellular redox state (AsA/DHA and GSH/GSSG) by regulating the activities/contents of enzyme/non-enzyme involved in the AsA-GSH cycle. After Dap applications against stress, ROS accumulation (H2O2 content) and lipid peroxidation (TBARS) were effectively reduced. The findings showed that by eliminating As-induced oxidative damage and protecting the biochemical processes of photosynthesis, Dap treatments have a substantial potential to give resistance to wheat 
650 4 |a Journal Article 
650 4 |a 1,3-Diaminopropane 
650 4 |a Antioxidant 
650 4 |a Arsenic 
650 4 |a PSII photochemistry 
650 4 |a Triticum aestivum 
650 7 |a Antioxidants  |2 NLM 
650 7 |a Arsenic  |2 NLM 
650 7 |a N712M78A8G  |2 NLM 
650 7 |a Polyamines  |2 NLM 
650 7 |a Thiobarbituric Acid Reactive Substances  |2 NLM 
650 7 |a Hydrogen Peroxide  |2 NLM 
650 7 |a BBX060AN9V  |2 NLM 
650 7 |a trimethylenediamine  |2 NLM 
650 7 |a CB3ISL56KG  |2 NLM 
650 7 |a Ascorbic Acid  |2 NLM 
650 7 |a PQ6CK8PD0R  |2 NLM 
650 7 |a Glutathione  |2 NLM 
650 7 |a GAN16C9B8O  |2 NLM 
650 7 |a Peroxidase  |2 NLM 
650 7 |a EC 1.11.1.7  |2 NLM 
650 7 |a Glutathione Peroxidase  |2 NLM 
650 7 |a EC 1.11.1.9  |2 NLM 
650 7 |a Chlorophyll  |2 NLM 
650 7 |a 1406-65-1  |2 NLM 
700 1 |a Alp-Turgut, Fatma Nur  |e verfasserin  |4 aut 
700 1 |a Arikan, Busra  |e verfasserin  |4 aut 
700 1 |a Tofan, Aysenur  |e verfasserin  |4 aut 
700 1 |a Ozfidan-Konakci, Ceyda  |e verfasserin  |4 aut 
700 1 |a Yildiztugay, Evren  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Plant physiology and biochemistry : PPB  |d 1991  |g 201(2023) vom: 15. Aug., Seite 107886  |w (DE-627)NLM098178261  |x 1873-2690  |7 nnns 
773 1 8 |g volume:201  |g year:2023  |g day:15  |g month:08  |g pages:107886 
856 4 0 |u http://dx.doi.org/10.1016/j.plaphy.2023.107886  |3 Volltext 
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