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231223s2010 xx |||||o 00| ||eng c |
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|a 10.1021/la903799n
|2 doi
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|a pubmed24n0649.xml
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|a (DE-627)NLM194771075
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|a (NLM)20121055
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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1 |
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|a Zhou, Haojie
|e verfasserin
|4 aut
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|a Noncovalent attachment of NAD+ cofactor onto carbon nanotubes for preparation of integrated dehydrogenase-based electrochemical biosensors
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|c 2010
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 01.07.2010
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|a Date Revised 21.11.2013
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|a published: Print
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|a Citation Status MEDLINE
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|a This study describes a facile approach to the preparation of integrated dehydrogenase-based electrochemical biosensors through noncovalent attachment of an oxidized form of beta-nicotinamide adenine dinucleotide (NAD(+)) onto carbon nanotubes with the interaction between the adenine subunit in NAD(+) molecules and multiwalled carbon nanotubes (MWCNTs). X-ray photoelectron spectroscopic and cyclic voltammetric results suggest that NAD(+) is noncovalently attached onto MWCNTs to form an NAD(+)/MWCNT composite that acts as the electronic transducer for the integrated dehydrogenase-based electrochemical biosensors. With glucose dehydrogenase (GDH) as a model dehydrogenase-based recognition unit, electrochemical studies reveal that glucose is readily oxidized at the GDH/NAD(+)/MWCNT-modified electrode without addition of NAD(+) in the phosphate buffer. The potential for the oxidation of glucose at the GDH/NAD(+)/MWCNT-modified electrode remains very close to that for NADH oxidation at the MWCNT-modified electrode, but it is more negative than those for the oxidation of glucose at the MWCNT-modified electrode and for NADH oxidation at a bare glassy carbon electrode. These results demonstrate that NAD(+) molecules stably attached onto MWCNTs efficiently act as the cofactor for the dehydrogenases. MWCNTs employed here not only serve as the electronic transducer and the support to confine NAD(+) cofactor onto the electrode surface, but also act as the electrocatalyst for NADH oxidation in the dehydrogenase-based electrochemical biosensors. At the GDH/NAD(+)/MWCNT-based glucose biosensor, the current is linear with the concentration of glucose being within a concentration range from 10 to 300 microM with a limit of detection down to 4.81 microM (S/N = 3). This study offers a facile and versatile approach to the development of integrated dehydrogenase-based electrochemical devices, such as electrochemical biosensors and biofuel cells
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Research Support, U.S. Gov't, Non-P.H.S.
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|a Nanotubes, Carbon
|2 NLM
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|a NAD
|2 NLM
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|a 0U46U6E8UK
|2 NLM
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|a Glucose 1-Dehydrogenase
|2 NLM
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|a EC 1.1.1.47
|2 NLM
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1 |
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|a Zhang, Zipin
|e verfasserin
|4 aut
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1 |
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|a Yu, Ping
|e verfasserin
|4 aut
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700 |
1 |
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|a Su, Lei
|e verfasserin
|4 aut
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1 |
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|a Ohsaka, Takeo
|e verfasserin
|4 aut
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1 |
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|a Mao, Lanqun
|e verfasserin
|4 aut
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773 |
0 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 26(2010), 8 vom: 20. Apr., Seite 6028-32
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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1 |
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|g volume:26
|g year:2010
|g number:8
|g day:20
|g month:04
|g pages:6028-32
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|u http://dx.doi.org/10.1021/la903799n
|3 Volltext
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|d 26
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