期刊
NEW PHYTOLOGIST
卷 202, 期 3, 页码 920-928出版社
WILEY
DOI: 10.1111/nph.12715
关键词
chloroplast envelope membranes; ferric chelate reductase activity; ferric chelate oxidoreductase; iron deficiency; iron uptake
资金
- ERA Chemistry - OTKA [NN-84307]
- Chinese-Hungarian Bilateral Cooperation [TET_12_CN-1-2012-0025]
Iron (Fe) has an essential role in the biosynthesis of chlorophylls and redox cofactors, and thus chloroplast iron uptake is a process of special importance. The chloroplast ferric chelate oxidoreductase (cFRO) has a crucial role in this process but it is poorly characterized. To study the localization and mechanism of action of cFRO, sugar beet (Beta vulgaris cv Orbis) chloroplast envelope fractions were isolated by gradient ultracentrifugation, and their purity was tested by western blotting against different marker proteins. The ferric chelate reductase (FCR) activity of envelope fractions was studied in the presence of NAD(P)H (reductants) and FAD coenzymes. Reduction of Fe(III)-ethylenediaminetetraacetic acid was monitored spectrophotometrically by the Fe(II)-bathophenanthroline disulfonate complex formation. FCR activity, that is production of free Fe(II) for Fe uptake, showed biphasic saturation kinetics, and was clearly associated only to chloroplast inner envelope (cIE) vesicles. The reaction rate was >2.5 times higher with NADPH than with NADH, which indicates the natural coenzyme preference of cFRO activity and its dependence on photosynthesis. FCR activity of cIE vesicles isolated from Fe-deficient plants also showed clear biphasic kinetics, where the K-M of the low affinity component was elevated, and thus this component was down-regulated.
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