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Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris

Laccases (E.C. 1.10.3.2) are multicopper oxidases of great importance in the industry due to their non-specificity and high oxidative potential. Laccases are useful to bleach synthetic dyes, oxidize phenolic compounds and degrade pesticides, among others. Hence, the objective of this work was to opt...

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Autores principales: Ardila-Leal, Leidy D., Alvarado-Ramírez, María F., Gutiérrez-Rojas, Ivonne S., Poutou-Piñales, Raúl A., Quevedo-Hidalgo, Balkys, Pérez-Flórez, Alejandro, Pedroza-Rodríguez, Aura M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184261/
https://www.ncbi.nlm.nih.gov/pubmed/32368658
http://dx.doi.org/10.1016/j.heliyon.2020.e03852
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author Ardila-Leal, Leidy D.
Alvarado-Ramírez, María F.
Gutiérrez-Rojas, Ivonne S.
Poutou-Piñales, Raúl A.
Quevedo-Hidalgo, Balkys
Pérez-Flórez, Alejandro
Pedroza-Rodríguez, Aura M.
author_facet Ardila-Leal, Leidy D.
Alvarado-Ramírez, María F.
Gutiérrez-Rojas, Ivonne S.
Poutou-Piñales, Raúl A.
Quevedo-Hidalgo, Balkys
Pérez-Flórez, Alejandro
Pedroza-Rodríguez, Aura M.
author_sort Ardila-Leal, Leidy D.
collection PubMed
description Laccases (E.C. 1.10.3.2) are multicopper oxidases of great importance in the industry due to their non-specificity and high oxidative potential. Laccases are useful to bleach synthetic dyes, oxidize phenolic compounds and degrade pesticides, among others. Hence, the objective of this work was to optimize low cost culture media for recombinant (rPOXA 1B) laccase production from Pleurotus ostreatus in Pichia pastoris. To this end, low cost nitrogen sources were studied, such as malt extract, isolated soy protein and milk serum. Following, two central composite designs (CCD) were performed. In CCD-1 different concentrations of glucose USP (0–13.35 gL(-1)), protein isolated soy protein (5–25 gL(-1)), malt extract (3.5–17.5 gL(-1)) and (NH(4))(2)SO(4) (1.3–6.5 gL(-1)) were evaluated. In CCD-2 only different concentrations of glucose USP (7.9–22 gL(-1)) and isolated soy protein (15.9–44.9 gL(-1)) were evaluated. CCD-2 results led to a One Factor Experimental design (OFED) to evaluate higher isolated soy protein (20–80 gL(-1)) concentrations. In all designs, (CCD-1, CCD-2 and OFED) CuSO(4) (0.16 gL(-1)) and chloramphenicol (0.1 gL(-1)) concentrations remained unchanged. For the OFED after sequential statistical optimization, an enzyme activity of 12,877.3 ± 481.2 UL(−1) at 168 h was observed. rPOXA 1B activity increased 30.54 % in comparison with CCD-2 results. Final composition of optimized media was: 20 gL(-1) glucose USP, 50 gL(-1) isolated soy protein 90 % (w/w), 11.74 gL(-1) malt extract, and 4.91 gL(-1) (NH(4))(2)SO(4). With this culture media, it was possible to reduce culture media costs by 89.84 % in comparison with improved culture media previously described by our group.
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spelling pubmed-71842612020-05-04 Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris Ardila-Leal, Leidy D. Alvarado-Ramírez, María F. Gutiérrez-Rojas, Ivonne S. Poutou-Piñales, Raúl A. Quevedo-Hidalgo, Balkys Pérez-Flórez, Alejandro Pedroza-Rodríguez, Aura M. Heliyon Article Laccases (E.C. 1.10.3.2) are multicopper oxidases of great importance in the industry due to their non-specificity and high oxidative potential. Laccases are useful to bleach synthetic dyes, oxidize phenolic compounds and degrade pesticides, among others. Hence, the objective of this work was to optimize low cost culture media for recombinant (rPOXA 1B) laccase production from Pleurotus ostreatus in Pichia pastoris. To this end, low cost nitrogen sources were studied, such as malt extract, isolated soy protein and milk serum. Following, two central composite designs (CCD) were performed. In CCD-1 different concentrations of glucose USP (0–13.35 gL(-1)), protein isolated soy protein (5–25 gL(-1)), malt extract (3.5–17.5 gL(-1)) and (NH(4))(2)SO(4) (1.3–6.5 gL(-1)) were evaluated. In CCD-2 only different concentrations of glucose USP (7.9–22 gL(-1)) and isolated soy protein (15.9–44.9 gL(-1)) were evaluated. CCD-2 results led to a One Factor Experimental design (OFED) to evaluate higher isolated soy protein (20–80 gL(-1)) concentrations. In all designs, (CCD-1, CCD-2 and OFED) CuSO(4) (0.16 gL(-1)) and chloramphenicol (0.1 gL(-1)) concentrations remained unchanged. For the OFED after sequential statistical optimization, an enzyme activity of 12,877.3 ± 481.2 UL(−1) at 168 h was observed. rPOXA 1B activity increased 30.54 % in comparison with CCD-2 results. Final composition of optimized media was: 20 gL(-1) glucose USP, 50 gL(-1) isolated soy protein 90 % (w/w), 11.74 gL(-1) malt extract, and 4.91 gL(-1) (NH(4))(2)SO(4). With this culture media, it was possible to reduce culture media costs by 89.84 % in comparison with improved culture media previously described by our group. Elsevier 2020-04-25 /pmc/articles/PMC7184261/ /pubmed/32368658 http://dx.doi.org/10.1016/j.heliyon.2020.e03852 Text en © 2020 The Author(s) 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 Article
Ardila-Leal, Leidy D.
Alvarado-Ramírez, María F.
Gutiérrez-Rojas, Ivonne S.
Poutou-Piñales, Raúl A.
Quevedo-Hidalgo, Balkys
Pérez-Flórez, Alejandro
Pedroza-Rodríguez, Aura M.
Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris
title Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris
title_full Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris
title_fullStr Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris
title_full_unstemmed Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris
title_short Low-cost media statistical design for laccase rPOXA 1B production in P. pastoris
title_sort low-cost media statistical design for laccase rpoxa 1b production in p. pastoris
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184261/
https://www.ncbi.nlm.nih.gov/pubmed/32368658
http://dx.doi.org/10.1016/j.heliyon.2020.e03852
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