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Substrate specificity of a new laccase from Trametes polyzona WRF03

Various aromatic compounds that are structurally analogous to lignin were tested as possible/preferred substrates for purified laccase from newly isolated white rote fungi, Trametes polyzona WRF03. The pH optima were tested using different substrates and kinetic studies were conducted at these pH op...

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Autores principales: Ezike, Tobechukwu C., Udeh, Jerry O., Joshua, Parker E., Ezugwu, Arinze L., Isiwu, Chukwurobe V., Eze, Sabinus O.O., Chilaka, Ferdinand C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841367/
https://www.ncbi.nlm.nih.gov/pubmed/33537494
http://dx.doi.org/10.1016/j.heliyon.2021.e06080
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author Ezike, Tobechukwu C.
Udeh, Jerry O.
Joshua, Parker E.
Ezugwu, Arinze L.
Isiwu, Chukwurobe V.
Eze, Sabinus O.O.
Chilaka, Ferdinand C.
author_facet Ezike, Tobechukwu C.
Udeh, Jerry O.
Joshua, Parker E.
Ezugwu, Arinze L.
Isiwu, Chukwurobe V.
Eze, Sabinus O.O.
Chilaka, Ferdinand C.
author_sort Ezike, Tobechukwu C.
collection PubMed
description Various aromatic compounds that are structurally analogous to lignin were tested as possible/preferred substrates for purified laccase from newly isolated white rote fungi, Trametes polyzona WRF03. The pH optima were tested using different substrates and kinetic studies were conducted at these pH optima. The pH optima in the presence of ABTS, α-naphthol, o-dianisidine, and catechol were 4.5 but 5.0 and 5.5 in the presence of guaiacol and pyrogallol, respectively. The initial velocities obtained from the kinetic study were analyzed using Graph Pad Prism 7 and Lineweaver-Burk plot to obtain kinetic constants (k(m) and (Vmax)) which were used to calculate substrate specificity. Amongst all the substrates tested, ABTS had the highest specificity-constant (181.51 M(−1)s(−1)), and therefore, the most preferred substrate was followed by α-naphthol, o-dianisidine, guaiacol, pyrogallol, and catechol. Resorcinol, orcinol, and veratryl alcohol did not display any considerable chemical shift in the presence of Trametes polyzona WRF03 laccase. Also, oxidation of phenolic substrates appeared to be dependent on the nature of the substituent groups and their relative position on the aromatic nucleus. Since most of these substrates are structural analogs of lignin and many recalcitrant environmental pollutants, the enzyme may find application in delignification, treatment of wastewater containing dyes, and polycyclic aromatic hydrocarbons (PAHs).
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spelling pubmed-78413672021-02-02 Substrate specificity of a new laccase from Trametes polyzona WRF03 Ezike, Tobechukwu C. Udeh, Jerry O. Joshua, Parker E. Ezugwu, Arinze L. Isiwu, Chukwurobe V. Eze, Sabinus O.O. Chilaka, Ferdinand C. Heliyon Research Article Various aromatic compounds that are structurally analogous to lignin were tested as possible/preferred substrates for purified laccase from newly isolated white rote fungi, Trametes polyzona WRF03. The pH optima were tested using different substrates and kinetic studies were conducted at these pH optima. The pH optima in the presence of ABTS, α-naphthol, o-dianisidine, and catechol were 4.5 but 5.0 and 5.5 in the presence of guaiacol and pyrogallol, respectively. The initial velocities obtained from the kinetic study were analyzed using Graph Pad Prism 7 and Lineweaver-Burk plot to obtain kinetic constants (k(m) and (Vmax)) which were used to calculate substrate specificity. Amongst all the substrates tested, ABTS had the highest specificity-constant (181.51 M(−1)s(−1)), and therefore, the most preferred substrate was followed by α-naphthol, o-dianisidine, guaiacol, pyrogallol, and catechol. Resorcinol, orcinol, and veratryl alcohol did not display any considerable chemical shift in the presence of Trametes polyzona WRF03 laccase. Also, oxidation of phenolic substrates appeared to be dependent on the nature of the substituent groups and their relative position on the aromatic nucleus. Since most of these substrates are structural analogs of lignin and many recalcitrant environmental pollutants, the enzyme may find application in delignification, treatment of wastewater containing dyes, and polycyclic aromatic hydrocarbons (PAHs). Elsevier 2021-01-25 /pmc/articles/PMC7841367/ /pubmed/33537494 http://dx.doi.org/10.1016/j.heliyon.2021.e06080 Text en © 2021 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Ezike, Tobechukwu C.
Udeh, Jerry O.
Joshua, Parker E.
Ezugwu, Arinze L.
Isiwu, Chukwurobe V.
Eze, Sabinus O.O.
Chilaka, Ferdinand C.
Substrate specificity of a new laccase from Trametes polyzona WRF03
title Substrate specificity of a new laccase from Trametes polyzona WRF03
title_full Substrate specificity of a new laccase from Trametes polyzona WRF03
title_fullStr Substrate specificity of a new laccase from Trametes polyzona WRF03
title_full_unstemmed Substrate specificity of a new laccase from Trametes polyzona WRF03
title_short Substrate specificity of a new laccase from Trametes polyzona WRF03
title_sort substrate specificity of a new laccase from trametes polyzona wrf03
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841367/
https://www.ncbi.nlm.nih.gov/pubmed/33537494
http://dx.doi.org/10.1016/j.heliyon.2021.e06080
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