Towards structural studies of the old yellow enzyme homologue SYE4 from Shewanella oneidensis and its complexes at atomic resolution.

Jonathan Elegheert, Debbie van den Hemel, Ina Dix, Jan Stout, Jozef Van Beeumen, Ann Brigé, Savvas N. Savvides
Acta Cryst Sect F. 2009-12-25; 66(1): 85-90
DOI: 10.1107/S1744309109050386

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1. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 Jan 1;66(Pt 1):85-90. doi: 10.1107/S1744309109050386. Epub 2009 Dec 25.

Towards structural studies of the old yellow enzyme homologue SYE4 from Shewanella oneidensis and its complexes at atomic resolution.

Elegheert J(1), van den Hemel D, Dix I, Stout J, Van Beeumen J, Brigé A, Savvides SN.

Author information:
(1)Department of Biochemistry and Microbiology, Laboratory for Protein Biochemistry and Biomolecular Engineering (L-ProBE), Ghent University, K. L. Ledeganckstraat 35, 9000 Ghent, Belgium.

Shewanella oneidensis is an environmentally versatile Gram-negative gamma-proteobacterium that is endowed with an unusually large proteome of redox proteins. Of the four old yellow enzyme (OYE) homologues found in S. oneidensis,
SYE4 is the homologue most implicated in resistance to oxidative stress. SYE4 was recombinantly expressed in Escherichia coli, purified and crystallized using the hanging-drop vapour-diffusion method. The crystals belonged to the orthorhombic space group P2(1)2(1)2(1) and were moderately pseudo-merohedrally twinned, emulating a P422 metric symmetry. The native crystals of SYE4 were of exceptional diffraction quality and provided complete data to 1.10 A resolution using synchrotron radiation, while crystals of the reduced enzyme and of the enzyme in complex with a wide range of ligands typically led to high-quality complete data sets to 1.30-1.60 A resolution, thus providing a rare opportunity to dissect the structure-function relationships of a good-sized enzyme (40 kDa) at true atomic
resolution. Here, the attainment of a number of experimental milestones in the crystallographic studies of SYE4 and its complexes are reported, including isolation of the elusive hydride-Meisenheimer complex.

DOI: 10.1107/S1744309109050386
PMCID: PMC2805545
PMID: 20057079 [Indexed for MEDLINE]

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