-
Something wrong with this record ?
Interplay between antioxidants in response to photooxidative stress in Arabidopsis
A. Kumar, A. Prasad, M. Sedlářová, B. Ksas, M. Havaux, P. Pospíšil
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Antioxidants MeSH
- Arabidopsis * genetics MeSH
- Chloroplasts MeSH
- Light MeSH
- Tocopherols MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Tocochromanols (tocopherols, tocotrienols and plastochromanol-8), isoprenoid quinone (plastoquinone-9 and plastoquinol-9) and carotenoids (carotenes and xanthophylls), are lipid-soluble antioxidants in the chloroplasts, which play an important defensive role against photooxidative stress in plants. In this study, the interplay between the antioxidant activities of those compounds in excess light stress was analyzed in wild-type (WT) Arabidopsis thaliana and in a tocopherol cyclase mutant (vte1), a homogentisate phytyl transferase mutant (vte2) and a tocopherol cyclase overexpressor (VTE1oex). The results reveal a strategy of cooperation and replacement between α-tocopherol, plastochromanol-8, plastoquinone-9/plastoquinol-9 and zeaxanthin. In the first line of defense (non-radical mechanism), singlet oxygen is either physically or chemically quenched by α-tocopherol; however, when α-tocopherol is consumed, zeaxanthin and plastoquinone-9/plastoquinol-9 can provide alternative protection against singlet oxygen toxicity by functional replacement of α-tocopherol either by zeaxanthin for the physical quenching or by plastoquinone-9/plastoquinol-9 for the chemical quenching. When singlet oxygen escapes this first line of defense, it oxidizes lipids and forms lipid hydroperoxides, which are oxidized to lipid peroxyl radicals by ferric iron. In the second line of defense (radical mechanism), lipid peroxyl radicals are scavenged by α-tocopherol. After its consumption, plastochromanol-8 overtakes this function. We provide a comprehensive description of the reaction pathways underlying the non-radical and radical antioxidant activities of α-tocopherol, carotenoids, plastoquinone-9/plastoquinol-9 and plastochromanol-8. The interplay between the different plastid lipid-soluble antioxidants in the non-radical and the radical mechanism provides step by step insights into protection against photooxidative stress in higher plants.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21019807
- 003
- CZ-PrNML
- 005
- 20210830101419.0
- 007
- ta
- 008
- 210728s2020 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.freeradbiomed.2020.08.027 $2 doi
- 035 __
- $a (PubMed)32931882
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Kumar, Aditya $u Department of Biophysics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic
- 245 10
- $a Interplay between antioxidants in response to photooxidative stress in Arabidopsis / $c A. Kumar, A. Prasad, M. Sedlářová, B. Ksas, M. Havaux, P. Pospíšil
- 520 9_
- $a Tocochromanols (tocopherols, tocotrienols and plastochromanol-8), isoprenoid quinone (plastoquinone-9 and plastoquinol-9) and carotenoids (carotenes and xanthophylls), are lipid-soluble antioxidants in the chloroplasts, which play an important defensive role against photooxidative stress in plants. In this study, the interplay between the antioxidant activities of those compounds in excess light stress was analyzed in wild-type (WT) Arabidopsis thaliana and in a tocopherol cyclase mutant (vte1), a homogentisate phytyl transferase mutant (vte2) and a tocopherol cyclase overexpressor (VTE1oex). The results reveal a strategy of cooperation and replacement between α-tocopherol, plastochromanol-8, plastoquinone-9/plastoquinol-9 and zeaxanthin. In the first line of defense (non-radical mechanism), singlet oxygen is either physically or chemically quenched by α-tocopherol; however, when α-tocopherol is consumed, zeaxanthin and plastoquinone-9/plastoquinol-9 can provide alternative protection against singlet oxygen toxicity by functional replacement of α-tocopherol either by zeaxanthin for the physical quenching or by plastoquinone-9/plastoquinol-9 for the chemical quenching. When singlet oxygen escapes this first line of defense, it oxidizes lipids and forms lipid hydroperoxides, which are oxidized to lipid peroxyl radicals by ferric iron. In the second line of defense (radical mechanism), lipid peroxyl radicals are scavenged by α-tocopherol. After its consumption, plastochromanol-8 overtakes this function. We provide a comprehensive description of the reaction pathways underlying the non-radical and radical antioxidant activities of α-tocopherol, carotenoids, plastoquinone-9/plastoquinol-9 and plastochromanol-8. The interplay between the different plastid lipid-soluble antioxidants in the non-radical and the radical mechanism provides step by step insights into protection against photooxidative stress in higher plants.
- 650 _2
- $a antioxidancia $7 D000975
- 650 12
- $a Arabidopsis $x genetika $7 D017360
- 650 _2
- $a chloroplasty $7 D002736
- 650 _2
- $a světlo $7 D008027
- 650 _2
- $a tokoferoly $7 D024505
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Prasad, Ankush $u Department of Biophysics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic
- 700 1_
- $a Sedlářová, Michaela $u Department of Botany, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic
- 700 1_
- $a Ksas, Brigitte $u CEA, CNRS UMR 7265 BVME, Aix-Marseille Université, Laboratoire D'Écophysiologie Moléculaire des Plantes, CEA/Cadarache, F-13108, Saint-Paul-lez-Durance, France
- 700 1_
- $a Havaux, Michel $u CEA, CNRS UMR 7265 BVME, Aix-Marseille Université, Laboratoire D'Écophysiologie Moléculaire des Plantes, CEA/Cadarache, F-13108, Saint-Paul-lez-Durance, France
- 700 1_
- $a Pospíšil, Pavel $u Department of Biophysics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic. Electronic address: pavel.pospisil@upol.cz
- 773 0_
- $w MED00001857 $t Free radical biology & medicine $x 1873-4596 $g Roč. 160, č. - (2020), s. 894-907
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32931882 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20210830101419 $b ABA008
- 999 __
- $a ok $b bmc $g 1690589 $s 1140253
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 160 $c - $d 894-907 $e 20200912 $i 1873-4596 $m Free radical biology & medicine $n Free Radic Biol Med $x MED00001857
- LZP __
- $a Pubmed-20210728