Title of article :
Direct electrochemistry and environmental sensing of rice hemoglobin immobilized at graphite electrodes
Author/Authors :
Royo، نويسنده , , Beatriz and Sosna، نويسنده , , Maciej and Asensio، نويسنده , , Aaron C. and Moran، نويسنده , , Jose F. and Ferapontova، نويسنده , , Elena E.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
8
From page :
67
To page :
74
Abstract :
Non-symbiotic hemoglobin from rice (Oryza sativa L.), OsHb-1, with hexacoordinated rather than pentacoordinated heme and high affinity for oxygen, may have a particular role in O2 and environmental sensing. Here, a 21 kDa monomer OsHb-1 was electrochemically studied at graphite electrodes and further probed in analysis of environmental species such as hydrogen peroxide, cyanide, and superoxide. Redox potential of the OsHb-1 heme iron was found to be −136 mV vs. SCE, at pH 6.5, while the rate constant ks for the heterogeneous electron transfer (ET) between graphite and OsHb-1 immobilized in the Nafion membrane at the carbon nanotubes-modified electrodes was below 0.2 s−1. Despite sluggish ET, OsHb-1 efficiently, with current densities exceeding 2 mA cm−2 at −0.3 V, electrocatalyzed reduction of O2 starting from the potentials of OsHb-1 heme. The bioelectrocatalytic reduction of O2 was partially inhibited by CN− thus enabling its sensing down to a 100 pM level. Peroxidase-like activity of OsHb-1 and the reaction of the superoxide anion with the heme iron of OsHb-1, in de-oxygenated solutions, were studied and analysed in terms of OsHb-1 reactivity. The results obtained indicate OsHb-1 is a sensitive tool for environmental biosensing and toxicity screening.
Keywords :
Electron transfer , Rice hemoglobin , Ligand sensing: oxygen , Bioelectrocatalysis , hydrogen peroxide , Heme proteins , cyanide and superoxide
Journal title :
Journal of Electroanalytical Chemistry
Serial Year :
2013
Journal title :
Journal of Electroanalytical Chemistry
Record number :
1677364
Link To Document :
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