Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentation

Background: Tannases are enzymes with biotechnological potential produced mainly by microorganisms as filamentous fungi. In this context, the production and characterization of a multi-tolerant tannase from Aspergillus carbonarius is described. Results: The filamentous fungus A. carbonarius produced...

Full description

Bibliographic Details
Main Authors: Larissa Serrani Valera, João Atílio Jorge, Luis Henrique Souza Guimarães
Format: Article
Language:English
Published: Elsevier 2015-11-01
Series:Electronic Journal of Biotechnology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S071734581500127X
id doaj-7fdec753e8ca40f481b81006ab0b2af9
record_format Article
spelling doaj-7fdec753e8ca40f481b81006ab0b2af92020-11-24T23:01:48ZengElsevierElectronic Journal of Biotechnology0717-34582015-11-0118646447010.1016/j.ejbt.2015.09.008Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentationLarissa Serrani Valera0João Atílio Jorge1Luis Henrique Souza Guimarães2Instituto de Química de Araraquara, Universidade Estadual Paulista “Júlio de Mesquita Filho”, Rua Prof. Mario Degni s/n, Quitandinha, 14800-900 Araraquara, São Paulo, BrazilDepartamento de Biologia, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Avenida Bandeirantes 3900, Monte Alegre, 14040-901 Ribeirão Preto, São Paulo, BrazilDepartamento de Biologia, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Avenida Bandeirantes 3900, Monte Alegre, 14040-901 Ribeirão Preto, São Paulo, BrazilBackground: Tannases are enzymes with biotechnological potential produced mainly by microorganisms as filamentous fungi. In this context, the production and characterization of a multi-tolerant tannase from Aspergillus carbonarius is described. Results: The filamentous fungus A. carbonarius produced high levels of tannase when cultivated under solid-state fermentation using green tea leaves as substrate/carbon source and tap water at a 1:1 ratio as the moisture agent for 72 h at 30°C. Two tannase activity peaks were obtained during the purification step using DEAE-Cellulose. The second peak (peak II) was purified 11-fold with 14% recovery from a Sepharose CL-6B chromatographic column. The tannase from peak II (tannase II) was characterized as a heterodimeric glycoprotein of 134.89 kDa, estimated through gel filtration, with subunits of 65 kDa and 100 kDa, estimated through SDS-PAGE, and 48% carbohydrate content. The optimal temperature and pH for tannase II activity was 60°C and 5.0, respectively. The enzyme was fully stable at temperatures ranging from 20–60°C for 120 min, and the half-life (T1/2) at 75°C was 62 min. The activation energy was 28.93 kJ/mol. After incubation at pH 5.0 for 60 min, 75% of the enzyme activity was maintained. However, enzyme activity was increased in the presence of AgNO3 and it was tolerant to solvents and detergents. Tannase II exhibited a better affinity for methyl gallate (Km = 1.42 mM) rather than for tannic acid (Km = 2.2 mM). Conclusion: A. carbonarius tannase presented interesting properties as, for example, multi-tolerance, which highlight its potential for future application.http://www.sciencedirect.com/science/article/pii/S071734581500127XAspergillusMicrobial enzymesSolid-state fermentationTannaseTannic acid
collection DOAJ
language English
format Article
sources DOAJ
author Larissa Serrani Valera
João Atílio Jorge
Luis Henrique Souza Guimarães
spellingShingle Larissa Serrani Valera
João Atílio Jorge
Luis Henrique Souza Guimarães
Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentation
Electronic Journal of Biotechnology
Aspergillus
Microbial enzymes
Solid-state fermentation
Tannase
Tannic acid
author_facet Larissa Serrani Valera
João Atílio Jorge
Luis Henrique Souza Guimarães
author_sort Larissa Serrani Valera
title Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentation
title_short Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentation
title_full Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentation
title_fullStr Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentation
title_full_unstemmed Characterization of a multi-tolerant tannin acyl hydrolase II from Aspergillus carbonarius produced under solid-state fermentation
title_sort characterization of a multi-tolerant tannin acyl hydrolase ii from aspergillus carbonarius produced under solid-state fermentation
publisher Elsevier
series Electronic Journal of Biotechnology
issn 0717-3458
publishDate 2015-11-01
description Background: Tannases are enzymes with biotechnological potential produced mainly by microorganisms as filamentous fungi. In this context, the production and characterization of a multi-tolerant tannase from Aspergillus carbonarius is described. Results: The filamentous fungus A. carbonarius produced high levels of tannase when cultivated under solid-state fermentation using green tea leaves as substrate/carbon source and tap water at a 1:1 ratio as the moisture agent for 72 h at 30°C. Two tannase activity peaks were obtained during the purification step using DEAE-Cellulose. The second peak (peak II) was purified 11-fold with 14% recovery from a Sepharose CL-6B chromatographic column. The tannase from peak II (tannase II) was characterized as a heterodimeric glycoprotein of 134.89 kDa, estimated through gel filtration, with subunits of 65 kDa and 100 kDa, estimated through SDS-PAGE, and 48% carbohydrate content. The optimal temperature and pH for tannase II activity was 60°C and 5.0, respectively. The enzyme was fully stable at temperatures ranging from 20–60°C for 120 min, and the half-life (T1/2) at 75°C was 62 min. The activation energy was 28.93 kJ/mol. After incubation at pH 5.0 for 60 min, 75% of the enzyme activity was maintained. However, enzyme activity was increased in the presence of AgNO3 and it was tolerant to solvents and detergents. Tannase II exhibited a better affinity for methyl gallate (Km = 1.42 mM) rather than for tannic acid (Km = 2.2 mM). Conclusion: A. carbonarius tannase presented interesting properties as, for example, multi-tolerance, which highlight its potential for future application.
topic Aspergillus
Microbial enzymes
Solid-state fermentation
Tannase
Tannic acid
url http://www.sciencedirect.com/science/article/pii/S071734581500127X
work_keys_str_mv AT larissaserranivalera characterizationofamultitoleranttanninacylhydrolaseiifromaspergilluscarbonariusproducedundersolidstatefermentation
AT joaoatiliojorge characterizationofamultitoleranttanninacylhydrolaseiifromaspergilluscarbonariusproducedundersolidstatefermentation
AT luishenriquesouzaguimaraes characterizationofamultitoleranttanninacylhydrolaseiifromaspergilluscarbonariusproducedundersolidstatefermentation
_version_ 1725638729790390272