Title of article
NMR redox studies of flavocytochrome c3 from Shewanella frigidimarina
Author/Authors
Miguel Pessanha Pais، نويسنده , , David L. Turner، نويسنده , , Emma L. Rothery، نويسنده , , Katherine L. Pankhurst، نويسنده , , Graeme A. Reid، نويسنده , , Stephen K. Chapman، نويسنده , , Ant?nio V. Xavier، نويسنده , , Carlos A. Salgueiro، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2003
Pages
3
From page
379
To page
381
Abstract
Flavocytochrome c3 is a periplasmic fumarate reductase with Mr 63.8 kDa, isolated from Shewanella frigidimarina NCIMB400. NMR spectroscopy was tested for its potential to elucidate the oxidation profile of each of the four haem groups in the enzyme, using the strategy developed previously to perform the thermodynamic characterization of small tetrahaem cytochromes (FEBS Lett. 314 (1992) 155). This work shows that, despite the large size of the protein, 2D-NMR NOESY experiments can be used to obtain the network of chemical exchange connectivities, between the signals of specific haem groups in sequential oxidation stages.
Keywords
NMR , Paramagnetic shifts , Electron tranfer protein , Shewanella , Multihaem , Flavocytochrome
Journal title
INORGANICA CHIMICA ACTA
Serial Year
2003
Journal title
INORGANICA CHIMICA ACTA
Record number
1321855
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