TY - JOUR
T1 - Potential pulse-assisted immobilization of Myrothecium verrucaria bilirubin oxidase at planar and nanoporous gold electrodes
AU - Lopez, Francesca
AU - Siepenkoetter, Till
AU - Xiao, Xinxin
AU - Magner, Edmond
AU - Schuhmann, Wolfgang
AU - Salaj-Kosla, Urszula
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - A potential pulse-assisted approach was used to immobilize Myrothecium verrucaria bilirubin oxidase at planar and nanoporous gold electrodes (NPG) containing pores of ca. 20 nm and ca. 40 nm in diameter. An increase in the current due to the bioelectrocatalytic reduction of oxygen by MvBOD-modified gold electrodes obtained from a 20 μL drop by the proposed pulse-assisted approach was observed when compared to the response obtained with electrodes modified by drop-casting. This increase likely arises from a preferential orientation of MvBOD molecules at the planar gold surface obtained by fast switching of the potential pulses between opposite charges. The concomitant ion stirring effect induces the attraction of the enzymes to the charged gold surface and forces access to the internal pore volume of the NPG. Immobilization of MvBOD using the potential pulse-assisted approach significantly increases current densities by facilitating the electron transfer between the enzyme and the electrode surface.
AB - A potential pulse-assisted approach was used to immobilize Myrothecium verrucaria bilirubin oxidase at planar and nanoporous gold electrodes (NPG) containing pores of ca. 20 nm and ca. 40 nm in diameter. An increase in the current due to the bioelectrocatalytic reduction of oxygen by MvBOD-modified gold electrodes obtained from a 20 μL drop by the proposed pulse-assisted approach was observed when compared to the response obtained with electrodes modified by drop-casting. This increase likely arises from a preferential orientation of MvBOD molecules at the planar gold surface obtained by fast switching of the potential pulses between opposite charges. The concomitant ion stirring effect induces the attraction of the enzymes to the charged gold surface and forces access to the internal pore volume of the NPG. Immobilization of MvBOD using the potential pulse-assisted approach significantly increases current densities by facilitating the electron transfer between the enzyme and the electrode surface.
KW - Blue multi-copper oxidases
KW - Enzyme immobilization
KW - Myrothecium verrucaria bilirubin oxidase
KW - Nanoporous gold (NPG)
KW - Potential pulse-assisted immobilization
UR - http://www.scopus.com/inward/record.url?scp=85039436523&partnerID=8YFLogxK
U2 - 10.1016/j.jelechem.2017.12.023
DO - 10.1016/j.jelechem.2017.12.023
M3 - Article
AN - SCOPUS:85039436523
SN - 1572-6657
VL - 812
SP - 194
EP - 198
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
ER -