Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 445765
Title Communication between L-galactono-¿-lactone dehydrogenase and cytochrome c.
Author(s) Hervas, M.; Bashir, Q.; Leferink, N.G.H.; Ferreira, P.; Moreno-Beltran, J.B.; Westphal, A.H.; Diaz Moreno, I.; Medina, M.; La Rosa, M.A. De; Ubbink, M.; Navarro, J.A.; Berkel, W.J.H. van
Source FEBS Journal 280 (2013)8. - ISSN 1742-464X - p. 1830 - 1840.
DOI https://doi.org/10.1111/febs.12207
Department(s) Biochemistry
VLAG
Publication type Refereed Article in a scientific journal
Publication year 2013
Keyword(s) electron-transfer - nmr-spectroscopy - vitamin-c - yeast iso-1-cytochrome-c - arabidopsis-thaliana - protein interactions - kinetic-analysis - viologen analog - complex - plastocyanin
Abstract l-galactono-1,4-lactone dehydrogenase (GALDH) catalyzes the terminal step of vitamin C biosynthesis in plant mitochondria. Here we investigated the communication between Arabidopsis thaliana GALDH and its natural electron acceptor cytochrome c (Cc). Using laser-generated radicals we observed the formation and stabilization of the GALDH semiquinone anionic species (GALDHSQ ). GALDHSQ oxidation by Cc exhibited a nonlinear dependence on Cc concentration consistent with a kinetic mechanism involving protein-partner association to form a transient bimolecular complex prior to the electron transfer step. Oxidation of GALDHSQ by Cc was significantly impaired at high ionic strength, revealing the existence of attractive charge-charge interactions between the two reactants. Isothermal titration calorimetry showed that GALDH weakly interacts with both oxidized and reduced Cc. Chemical shift perturbations for (1) H and (15) N nuclei of Cc, arising from the interactions with unlabeled GALDH, were used to map the interacting surface of Cc. For Arabidopsis Cc and yeast Cc, similar residues are involved in the interaction with GALDH. These residues are confined to a single surface surrounding the heme edge. The range of chemical shift perturbations for the physiological Arabidopsis Cc-GALDH complex is larger than that of the non-physiological yeast Cc-GALDH complex, indicating that the former complex is more specific. In summary, the results point to a relatively low affinity GALDH-Cc interaction, similar for all partner redox states, involving protein-protein dynamic motions. Evidence is also provided that Cc utilizes a conserved surface surrounding the heme edge for the interaction with GALDH and other redox partners.
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