- The present study reports a facile approach for sulfite biosensing, based on enhanced direct electron transfer of a human sulfite oxidase (hSO) immobilized on a gold nanoparticles modified electrode. The spherical core shell AuNPs were prepared via a new method by reduction of HAuCl4 with branched poly(ethyleneimine) in an ionic liquids resulting particles with a diameter less than 10 nm. These nanoparticles were covalently attached to a mercaptoundecanoic acid modified Au-electrode where then hSO was adsorbed and an enhanced interfacial electron transfer and electrocatalysis was achieved. UV/Vis and resonance Raman spectroscopy, in combination with direct protein voltammetry, are employed for the characterization of the system and reveal no perturbation of the structural integrity of the redox protein. The proposed biosensor exhibited a quick steady-state current response, within 2 s, a linear detection range between 0.5 and 5.4 mu M with a high sensitivity (1.85 nA mu M-1). The investigated system provides remarkable advantages inThe present study reports a facile approach for sulfite biosensing, based on enhanced direct electron transfer of a human sulfite oxidase (hSO) immobilized on a gold nanoparticles modified electrode. The spherical core shell AuNPs were prepared via a new method by reduction of HAuCl4 with branched poly(ethyleneimine) in an ionic liquids resulting particles with a diameter less than 10 nm. These nanoparticles were covalently attached to a mercaptoundecanoic acid modified Au-electrode where then hSO was adsorbed and an enhanced interfacial electron transfer and electrocatalysis was achieved. UV/Vis and resonance Raman spectroscopy, in combination with direct protein voltammetry, are employed for the characterization of the system and reveal no perturbation of the structural integrity of the redox protein. The proposed biosensor exhibited a quick steady-state current response, within 2 s, a linear detection range between 0.5 and 5.4 mu M with a high sensitivity (1.85 nA mu M-1). The investigated system provides remarkable advantages in the possibility to work at low applied potential and at very high ionic strength. Therefore these properties could make the proposed system useful in the development of bioelectronic devices and its application in real samples.…
MetadatenAuthor details: | Stefano Frasca, Oscar Rojas, Johannes Salewski, Bettina NeumannORCiD, Konstanze Stiba, Inez M. Weidinger, Brigitte TierschORCiD, Silke LeimkühlerORCiDGND, Joachim KoetzORCiDGND, Ursula WollenbergerORCiDGND |
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DOI: | https://doi.org/10.1016/j.bioelechem.2011.11.012 |
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ISSN: | 1567-5394 |
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Title of parent work (English): | Bioelectrochemistry : an international journal devoted to electrochemical aspects of biology and biological aspects of electrochemistry ; official journal of the Bioelectrochemical Society |
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Publisher: | Elsevier |
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Place of publishing: | Lausanne |
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Publication type: | Article |
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Language: | English |
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Year of first publication: | 2012 |
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Publication year: | 2012 |
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Release date: | 2017/03/26 |
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Tag: | Direct electron transfer; Gold nanoparticle; Human sulfite oxidase; Ionic liquid; Sulfite biosensor |
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Volume: | 87 |
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Number of pages: | 9 |
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First page: | 33 |
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Last Page: | 41 |
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Funding institution: | Cluster of Excellence "Unifying Concepts in Catalysis"; Deutsche
Forschungsgemeinschaft [EXC 314, SM 199/7-1]; ILB (TERAsens); Fonds der
Chemischen Industrie; National University of Costa Rica; National
Science Bureau of Costa Rica (MICIT); National Science Bureau of Costa
Rica (CONICIT); DAAD |
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Organizational units: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie |
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Peer review: | Referiert |
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