Production and Catalytic Properties of Amylases fromLichtheimia ramosaandThermoascus aurantiacusby Solid-State Fermentation

Author:

de Oliveira Ana Paula Aguero1,Silvestre Maria Alice1,Garcia Nayara Fernanda Lisboa1,Alves-Prado Heloíza Ferreira2,Rodrigues André3,Paz Marcelo Fossa da1,Fonseca Gustavo Graciano4,Leite Rodrigo Simões Ribeiro1ORCID

Affiliation:

1. Laboratory of Enzymology and Fermentation Processes, Faculty of Biological and Environmental Sciences, Federal University of Grande Dourados (FCBA/UFGD), Rodovia Dourados/Itahum, km 12, 79804-970 Dourados, MS, Brazil

2. Faculty of Engineering, Department of Phytotechnology, Food Technology and Social Economy, São Paulo State University (FEIS/UNESP), Avenida Brasil, No. 56, 15385-000 Ilha Solteira, SP, Brazil

3. Laboratory of Fungal Ecology and Systematics, Biosciences Institute, Department of Biochemistry and Microbiology, São Paulo State University (IB/UNESP), Avenida 24A, No. 1515, 13506-900 Rio Claro, SP, Brazil

4. Laboratory of Bioengineering, Faculty of Biological and Environmental Sciences, Federal University of Grande Dourados (FCBA/UFGD), Rodovia Dourados/Itahum, km 12, 79804-970 Dourados, MS, Brazil

Abstract

The present study compared the production and the catalytic properties of amylolytic enzymes obtained from the fungiLichtheimia ramosa(mesophilic) andThermoascus aurantiacus(thermophilic). The highest amylase production in both fungi was observed in wheat bran supplemented with nutrient solution (pH 4.0) after 96 hours of cultivation, reaching 417.2 U/g of dry substrate (or 41.72 U/mL) and 144.5 U/g of dry substrate (or 14.45 U/mL) forL. ramosaandT. aurantiacus, respectively. The enzymes showed higher catalytic activity at pH 6.0 at 60°C. The amylases produced byL. ramosaandT. aurantiacuswere stable between pH 3.5–10.5 and pH 4.5–9.5, respectively. The amylase ofL. ramosawas stable at 55°C after 1 hour of incubation, whereas that ofT. aurantiacusmaintained 60% of its original activity under the same conditions. Both enzymes were active in the presence of ethanol. The enzymes hydrolyzed starch from different sources, with the best results obtained with corn starch. The enzymatic complex produced byL. ramosashowed dextrinizing and saccharifying potential. The enzymatic extract produced by the fungusT. aurantiacuspresented only saccharifying potential, releasing glucose monomers as the main hydrolysis product.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Hindawi Limited

Subject

General Environmental Science,General Biochemistry, Genetics and Molecular Biology,General Medicine

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