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Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme
In this paper we report the successful use of a non-metallic electrode material, boron-doped diamond (BDD), for the anodic electro-oxidative modification of hen egg white lysozyme (HEWL). Platinum electrodes can give rise to loss of activity of HEWL in electrosynthetic studies, whereas activity is r...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101334/ https://www.ncbi.nlm.nih.gov/pubmed/21760652 http://dx.doi.org/10.1016/j.enzmictec.2010.02.002 |
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author | Iniesta, Jesús Esclapez-Vicente, María Deseada Heptinstall, John Walton, David J. Peterson, Ian R. Mikhailov, Victor A. Cooper, Helen J. |
author_facet | Iniesta, Jesús Esclapez-Vicente, María Deseada Heptinstall, John Walton, David J. Peterson, Ian R. Mikhailov, Victor A. Cooper, Helen J. |
author_sort | Iniesta, Jesús |
collection | PubMed |
description | In this paper we report the successful use of a non-metallic electrode material, boron-doped diamond (BDD), for the anodic electro-oxidative modification of hen egg white lysozyme (HEWL). Platinum electrodes can give rise to loss of activity of HEWL in electrosynthetic studies, whereas activity is retained on boron-doped diamond which is proposed as an effective substitute material for this purpose. We also compare literature methods of electrode pre-treatment to determine the most effective in electrosynthesis. Our findings show a decrease in total nitroprotein yield with decreasing nitrite concentration and an increase with increasing solution pH, confirming that, at a BDD electrode, the controlling factor remains the concentration of tyrosine phenolate anion. Purification of mono- and bis-nitrated HEWL and assay of enzymic activity showed better retention of activity at BDD electrode surfaces when compared to platinum. The products from electro-oxidation of HEWL at BDD were confirmed by electrospray ionization Fourier transform ion cyclotron resonance (ESI-FT-ICR) mass spectrometry, which revealed unique mass increases of +45 and +90 Da for the mono- and bis-nitrated lysozyme, respectively, corresponding to nitration at tyrosine residues. The nitration sites were confirmed as Tyr23 and Tyr20. |
format | Text |
id | pubmed-3101334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-31013342011-07-12 Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme Iniesta, Jesús Esclapez-Vicente, María Deseada Heptinstall, John Walton, David J. Peterson, Ian R. Mikhailov, Victor A. Cooper, Helen J. Enzyme Microb Technol Article In this paper we report the successful use of a non-metallic electrode material, boron-doped diamond (BDD), for the anodic electro-oxidative modification of hen egg white lysozyme (HEWL). Platinum electrodes can give rise to loss of activity of HEWL in electrosynthetic studies, whereas activity is retained on boron-doped diamond which is proposed as an effective substitute material for this purpose. We also compare literature methods of electrode pre-treatment to determine the most effective in electrosynthesis. Our findings show a decrease in total nitroprotein yield with decreasing nitrite concentration and an increase with increasing solution pH, confirming that, at a BDD electrode, the controlling factor remains the concentration of tyrosine phenolate anion. Purification of mono- and bis-nitrated HEWL and assay of enzymic activity showed better retention of activity at BDD electrode surfaces when compared to platinum. The products from electro-oxidation of HEWL at BDD were confirmed by electrospray ionization Fourier transform ion cyclotron resonance (ESI-FT-ICR) mass spectrometry, which revealed unique mass increases of +45 and +90 Da for the mono- and bis-nitrated lysozyme, respectively, corresponding to nitration at tyrosine residues. The nitration sites were confirmed as Tyr23 and Tyr20. Elsevier 2010-05-05 /pmc/articles/PMC3101334/ /pubmed/21760652 http://dx.doi.org/10.1016/j.enzmictec.2010.02.002 Text en © 2010 Elsevier Inc. https://creativecommons.org/licenses/by/4.0/ Open Access under CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) license |
spellingShingle | Article Iniesta, Jesús Esclapez-Vicente, María Deseada Heptinstall, John Walton, David J. Peterson, Ian R. Mikhailov, Victor A. Cooper, Helen J. Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme |
title | Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme |
title_full | Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme |
title_fullStr | Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme |
title_full_unstemmed | Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme |
title_short | Retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme |
title_sort | retention of enzyme activity with a boron-doped diamond electrode in the electro-oxidative nitration of lysozyme |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101334/ https://www.ncbi.nlm.nih.gov/pubmed/21760652 http://dx.doi.org/10.1016/j.enzmictec.2010.02.002 |
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