LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase Cocktail

Cellulose is the most abundant polysaccharide in lignocellulosic biomass, where it is interlinked with lignin and hemicellulose. Bioethanol can be produced from biomass. Since breaking down biomass is difficult, cellulose-active enzymes secreted by filamentous fungi play an important role in degradi...

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Main Authors: Aline Vianna Bernardi, Luis Eduardo Gerolamo, Paula Fagundes de Gouvêa, Deborah Kimie Yonamine, Lucas Matheus Soares Pereira, Arthur Henrique Cavalcante de Oliveira, Sérgio Akira Uyemura, Taisa Magnani Dinamarco
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/1/276
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spelling doaj-3d7652520193497b96d0ac6127dde9a52020-12-30T00:05:52ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-12-012227627610.3390/ijms22010276LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase CocktailAline Vianna Bernardi0Luis Eduardo Gerolamo1Paula Fagundes de Gouvêa2Deborah Kimie Yonamine3Lucas Matheus Soares Pereira4Arthur Henrique Cavalcante de Oliveira5Sérgio Akira Uyemura6Taisa Magnani Dinamarco7Faculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-901, São Paulo, BrazilFaculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-901, São Paulo, BrazilFaculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-901, São Paulo, BrazilFaculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-901, São Paulo, BrazilFaculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-901, São Paulo, BrazilFaculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-901, São Paulo, BrazilFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-903, São Paulo, BrazilFaculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto 14040-901, São Paulo, BrazilCellulose is the most abundant polysaccharide in lignocellulosic biomass, where it is interlinked with lignin and hemicellulose. Bioethanol can be produced from biomass. Since breaking down biomass is difficult, cellulose-active enzymes secreted by filamentous fungi play an important role in degrading recalcitrant lignocellulosic biomass. We characterized a cellobiohydrolase (<i>Af</i>Cel6A) and lytic polysaccharide monooxygenase LPMO (<i>Af</i>AA9_B) from <i>Aspergillus fumigatus</i> after they were expressed in <i>Pichia pastoris</i> and purified. The biochemical parameters suggested that the enzymes were stable; the optimal temperature was ~60 °C. Further characterization revealed high turnover numbers (<i>k</i><sub>cat</sub> of 147.9 s<sup>−1</sup> and 0.64 s<sup>−1</sup>, respectively). Surprisingly, when combined, <i>Af</i>Cel6A and <i>Af</i>AA9_B did not act synergistically. <i>Af</i>Cel6A and <i>Af</i>AA9_B association inhibited <i>Af</i>Cel6A activity, an outcome that needs to be further investigated. However, <i>Af</i>Cel6A or <i>Af</i>AA9_B addition boosted the enzymatic saccharification activity of a cellulase cocktail and the activity of cellulase <i>Af</i>-EGL7. Enzymatic cocktail supplementation with <i>Af</i>Cel6A or <i>Af</i>AA9_B boosted the yield of fermentable sugars from complex substrates, especially sugarcane exploded bagasse, by up to 95%. The synergism between the cellulase cocktail and <i>Af</i>AA9_B was enzyme- and substrate-specific, which suggests a specific enzymatic cocktail for each biomass by up to 95%. The synergism between the cellulase cocktail and <i>Af</i>AA9_B was enzyme- and substrate-specific, which suggests a specific enzymatic cocktail for each biomass.https://www.mdpi.com/1422-0067/22/1/276GH6 cellobiohydrolaseAA9 LPMOlignocellulose hydrolysisbioethanol
collection DOAJ
language English
format Article
sources DOAJ
author Aline Vianna Bernardi
Luis Eduardo Gerolamo
Paula Fagundes de Gouvêa
Deborah Kimie Yonamine
Lucas Matheus Soares Pereira
Arthur Henrique Cavalcante de Oliveira
Sérgio Akira Uyemura
Taisa Magnani Dinamarco
spellingShingle Aline Vianna Bernardi
Luis Eduardo Gerolamo
Paula Fagundes de Gouvêa
Deborah Kimie Yonamine
Lucas Matheus Soares Pereira
Arthur Henrique Cavalcante de Oliveira
Sérgio Akira Uyemura
Taisa Magnani Dinamarco
LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase Cocktail
International Journal of Molecular Sciences
GH6 cellobiohydrolase
AA9 LPMO
lignocellulose hydrolysis
bioethanol
author_facet Aline Vianna Bernardi
Luis Eduardo Gerolamo
Paula Fagundes de Gouvêa
Deborah Kimie Yonamine
Lucas Matheus Soares Pereira
Arthur Henrique Cavalcante de Oliveira
Sérgio Akira Uyemura
Taisa Magnani Dinamarco
author_sort Aline Vianna Bernardi
title LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase Cocktail
title_short LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase Cocktail
title_full LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase Cocktail
title_fullStr LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase Cocktail
title_full_unstemmed LPMO <i>Af</i>AA9_B and Cellobiohydrolase <i>Af</i>Cel6A from <i>A. fumigatus</i> Boost Enzymatic Saccharification Activity of Cellulase Cocktail
title_sort lpmo <i>af</i>aa9_b and cellobiohydrolase <i>af</i>cel6a from <i>a. fumigatus</i> boost enzymatic saccharification activity of cellulase cocktail
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-12-01
description Cellulose is the most abundant polysaccharide in lignocellulosic biomass, where it is interlinked with lignin and hemicellulose. Bioethanol can be produced from biomass. Since breaking down biomass is difficult, cellulose-active enzymes secreted by filamentous fungi play an important role in degrading recalcitrant lignocellulosic biomass. We characterized a cellobiohydrolase (<i>Af</i>Cel6A) and lytic polysaccharide monooxygenase LPMO (<i>Af</i>AA9_B) from <i>Aspergillus fumigatus</i> after they were expressed in <i>Pichia pastoris</i> and purified. The biochemical parameters suggested that the enzymes were stable; the optimal temperature was ~60 °C. Further characterization revealed high turnover numbers (<i>k</i><sub>cat</sub> of 147.9 s<sup>−1</sup> and 0.64 s<sup>−1</sup>, respectively). Surprisingly, when combined, <i>Af</i>Cel6A and <i>Af</i>AA9_B did not act synergistically. <i>Af</i>Cel6A and <i>Af</i>AA9_B association inhibited <i>Af</i>Cel6A activity, an outcome that needs to be further investigated. However, <i>Af</i>Cel6A or <i>Af</i>AA9_B addition boosted the enzymatic saccharification activity of a cellulase cocktail and the activity of cellulase <i>Af</i>-EGL7. Enzymatic cocktail supplementation with <i>Af</i>Cel6A or <i>Af</i>AA9_B boosted the yield of fermentable sugars from complex substrates, especially sugarcane exploded bagasse, by up to 95%. The synergism between the cellulase cocktail and <i>Af</i>AA9_B was enzyme- and substrate-specific, which suggests a specific enzymatic cocktail for each biomass by up to 95%. The synergism between the cellulase cocktail and <i>Af</i>AA9_B was enzyme- and substrate-specific, which suggests a specific enzymatic cocktail for each biomass.
topic GH6 cellobiohydrolase
AA9 LPMO
lignocellulose hydrolysis
bioethanol
url https://www.mdpi.com/1422-0067/22/1/276
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