Interaction of ascorbate with photosystem I

• Published in: Photosynthesis research 2014-11, Vol.122 (2), p.215-231
• Main Authors: Trubitsin, Boris V, Mamedov, Mahir D, Semenov, Alexey Yu, Tikhonov, Alexander N
• Format: Article
• Language: English
• Subjects: Analysis; Antioxidants; Ascorbic Acid - chemistry; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Biochemistry; Biomedical and Life Sciences; Chloroplasts; cytochrome b; Defense industry; electron transfer; Electron transport; electron transport chain; Electron-Transferring Flavoproteins; electrons; free radicals; Gene Expression Regulation, Bacterial - physiology; ions; Life Sciences; Light; monitoring; mutants; Mutation; oxidants; photooxidation; Photosynthesis; photosystem I; Photosystem I Protein Complex - chemistry; photosystem II; Physiological aspects; Plant biology; Plant Genetics and Genomics; Plant Physiology; Plant Sciences; plastocyanin; Quinone; Regular Paper; spinach; Spinacia oleracea; Synechocystis; Synechocystis - genetics; Synechocystis - metabolism; Thylakoids
• ISSN: 0166-8595; 1573-5079
• DOI: 10.1007/s11120-014-0023-7

Ascorbate is one of the key participants of the antioxidant defense in plants. In this work, we have investigated the interaction of ascorbate with the chloroplast electron transport chain and isolated photosystem I (PSI), using the EPR method for monitoring the oxidized centers [Formula: see text] and ascorbate free radicals. Inhibitor analysis of the light-induced redox transients of P₇₀₀ in spinach thylakoids has demonstrated that ascorbate efficiently donates electrons to [Formula: see text] via plastocyanin. Inhibitors (DCMU and stigmatellin), which block electron transport between photosystem II and Pc, did not disturb the ascorbate capacity for electron donation to [Formula: see text]. Otherwise, inactivation of Pc with CN⁻ ions inhibited electron flow from ascorbate to [Formula: see text]. This proves that the main route of electron flow from ascorbate to [Formula: see text] runs through Pc, bypassing the plastoquinone (PQ) pool and the cytochrome b ₆ f complex. In contrast to Pc-mediated pathway, direct donation of electrons from ascorbate to [Formula: see text] is a rather slow process. Oxidized ascorbate species act as alternative oxidants for PSI, which intercept electrons directly from the terminal electron acceptors of PSI, thereby stimulating photooxidation of P₇₀₀. We investigated the interaction of ascorbate with PSI complexes isolated from the wild type cells and the MenB deletion strain of cyanobacterium Synechocystis sp. PCC 6803. In the MenB mutant, PSI contains PQ in the quinone-binding A₁-site, which can be substituted by high-potential electron carrier 2,3-dichloro-1,4-naphthoquinone (Cl₂NQ). In PSI from the MenB mutant with Cl₂NQ in the A₁-site, the outflow of electrons from PSI is impeded due to the uphill electron transfer from A₁ to the iron-sulfur cluster FX and further to the terminal clusters FA/FB, which manifests itself as a decrease in a steady-state level of [Formula: see text]. The addition of ascorbate promoted photooxidation of P₇₀₀ due to stimulation of electron outflow from PSI to oxidized ascorbate species. Thus, accepting electrons from PSI and donating them to [Formula: see text], ascorbate can mediate cyclic electron transport around PSI. The physiological significance of ascorbate-mediated electron transport is discussed.