Direct Bioelectrocatalysis of PQQ-Dependent Glucose Dehydrogenase
The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone‐dependent glucose dehydrogenase (PQQ‐dependent GDH) covalently attached to single‐walled carbon nanotubes (SWNTs). The homogeneous ink‐like SWNT suspension was used for both creating the SWNT network on the microelectrode c...
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Published in | Electroanalysis (New York, N.Y.) Vol. 19; no. 15; pp. 1562 - 1568 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Weinheim
WILEY-VCH Verlag
01.08.2007
WILEY‐VCH Verlag |
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Abstract | The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone‐dependent glucose dehydrogenase (PQQ‐dependent GDH) covalently attached to single‐walled carbon nanotubes (SWNTs). The homogeneous ink‐like SWNT suspension was used for both creating the SWNT network on the microelectrode carbon surface and for enzyme immobilization. Functionalization of the SWNT surface by forming active ester groups was found to considerably enhance SWNT solubility in water with a range from 0.1 to 1.0 mg/mL. The PQQ‐dependent GDH immobilized on the surface of the SWNTs exhibited fast heterogeneous electron transfer with a rate constant of 3.6 s−1. Moreover, the immobilized PQQ‐dependent GDH retained its enzymatic activity for glucose oxidation. A fusion of PQQ‐dependent GDH with SWNTs has a great potential for the development of low‐cost and reagentless glucose sensors and biofuel cells. |
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AbstractList | Abstract
The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone‐dependent glucose dehydrogenase (PQQ‐dependent GDH) covalently attached to single‐walled carbon nanotubes (SWNTs). The homogeneous ink‐like SWNT suspension was used for both creating the SWNT network on the microelectrode carbon surface and for enzyme immobilization. Functionalization of the SWNT surface by forming active ester groups was found to considerably enhance SWNT solubility in water with a range from 0.1 to 1.0 mg/mL. The PQQ‐dependent GDH immobilized on the surface of the SWNTs exhibited fast heterogeneous electron transfer with a rate constant of 3.6 s
−1
. Moreover, the immobilized PQQ‐dependent GDH retained its enzymatic activity for glucose oxidation. A fusion of PQQ‐dependent GDH with SWNTs has a great potential for the development of low‐cost and reagentless glucose sensors and biofuel cells. The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone‐dependent glucose dehydrogenase (PQQ‐dependent GDH) covalently attached to single‐walled carbon nanotubes (SWNTs). The homogeneous ink‐like SWNT suspension was used for both creating the SWNT network on the microelectrode carbon surface and for enzyme immobilization. Functionalization of the SWNT surface by forming active ester groups was found to considerably enhance SWNT solubility in water with a range from 0.1 to 1.0 mg/mL. The PQQ‐dependent GDH immobilized on the surface of the SWNTs exhibited fast heterogeneous electron transfer with a rate constant of 3.6 s−1. Moreover, the immobilized PQQ‐dependent GDH retained its enzymatic activity for glucose oxidation. A fusion of PQQ‐dependent GDH with SWNTs has a great potential for the development of low‐cost and reagentless glucose sensors and biofuel cells. The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone-dependent glucose dehydrogenase (PQQ-dependent GDH) covalently attached to single-walled carbon nanotubes (SWNTs). The homogeneous ink-like SWNT suspension was used for both creating the SWNT network on the microelectrode carbon surface and for enzyme immobilization. Functionalization of the SWNT surface by forming active ester groups was found to considerably enhance SWNT solubility in water with a range from 0.1 to 1.0mg/mL. The PQQ-dependent GDH immobilized on the surface of the SWNTs exhibited fast heterogeneous electron transfer with a rate constant of 3.6 s-1. Moreover, the immobilized PQQ-dependent GDH retained its enzymatic activity for glucose oxidation. A fusion of PQQ-dependent GDH with SWNTs has a great potential for the development of low-cost and reagentless glucose sensors and biofuel cells. |
Author | Apblett, Christopher Ivnitski, Dmitri Atanassov, Plamen |
Author_xml | – sequence: 1 givenname: Dmitri surname: Ivnitski fullname: Ivnitski, Dmitri email: ivnitski@unm.edu organization: Department of Chemical & Nuclear Engineering, University of New Mexico, Albuquerque, NM 87131, USA – sequence: 2 givenname: Plamen surname: Atanassov fullname: Atanassov, Plamen organization: Department of Chemical & Nuclear Engineering, University of New Mexico, Albuquerque, NM 87131, USA – sequence: 3 givenname: Christopher surname: Apblett fullname: Apblett, Christopher organization: Sandia National Laboratories, Albuquerque, NM, 87185, USA |
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Snippet | The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone‐dependent glucose dehydrogenase (PQQ‐dependent GDH) covalently attached to... Abstract The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone‐dependent glucose dehydrogenase (PQQ‐dependent GDH) covalently attached... The direct bioelectrocatalysis was demonstrated for pyrroloquinoline quinone-dependent glucose dehydrogenase (PQQ-dependent GDH) covalently attached to... |
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SubjectTerms | Carbon nanotubes Direct electron transfer Glucose PQQ-dependent glucose dehydrogenase |
Title | Direct Bioelectrocatalysis of PQQ-Dependent Glucose Dehydrogenase |
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