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Production, concentration and partial characterization of an enzymatic extract produced by an Aspergillus niger mutant in solid state fermentation.
Santos, Alex da Silva; Pereira, Gabriela Moysés; Mazotto de Almeida, Ana Maria; Santos, Regiane Ribeiro Dos; Terzi, Selma da Costa; Pacheco, Thályta Fraga; Beatriz Vermelho, Alane; Corrêa Cabral, Lourdes Maria; Couri, Sonia; Damaso, Mônica Caramez Triches.
Afiliação
  • Santos ADS; Departamento de Ciência e Tecnologia de Alimentos, Universidade Federal Rural do Rio de Janeiro, Seropédica, Brazil.
  • Pereira GM; Embrapa Agroindústria de Alimentos, Rio de Janeiro, Brazil.
  • Mazotto de Almeida AM; Instituto de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Santos RRD; Instituto de Microbiologia Prof Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Terzi SDC; Departamento de Ciência e Tecnologia de Alimentos, Universidade Federal Rural do Rio de Janeiro, Seropédica, Brazil.
  • Pacheco TF; Embrapa Agroindústria de Alimentos, Rio de Janeiro, Brazil.
  • Beatriz Vermelho A; Embrapa Agroindústria de Alimentos, Rio de Janeiro, Brazil.
  • Corrêa Cabral LM; Embrapa Agroenergia, Brasília, DF, Brazil.
  • Couri S; Instituto de Microbiologia Prof Paulo de Góes, BIOINOVAR, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Damaso MCT; Embrapa Agroindústria de Alimentos, Rio de Janeiro, Brazil.
Prep Biochem Biotechnol ; 52(10): 1109-1118, 2022.
Article em En | MEDLINE | ID: mdl-35175876
ABSTRACT
An enzymatic extract from Aspergillus niger 3T5B8 was produced by Solid State Fermentation (SSF) in aerated columns, using wheat bran as substrate. A combination of extracts produced using three different process conditions varying temperature, pH and aeration formed the final extract (Mixture). The Mixture was concentrated by an ultrafiltration process that partially purified and provided an efficient recovery of the enzymatic activities of xylanase (88.89%), polygalacturonase (89.3%), ß-glucosidase (93.15%), protease (98.68%) and carboxymethylcellulase (CMCase) (98.93%). SDS-PAGE analysis showed 15 visible protein bands in the crude and concentrated Mixture with molecular weights ranging from 15.1 to 104.6 kDa. Thin layer chromatography confirmed the effective action of ß-glucosidase and xylanase hydrolysis activities over cellobiose and xylan, respectively. A central composite design (CCD) with two variables and four replicates at the center points was used to determine the optimal temperature and pH for CMCase and ß-glucosidase. The optimal temperature was 78.9 °C and pH 3.8 for CMCase and 52.8 °C and pH 4.8 for ß-glucosidase, respectively.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aspergillus niger / Beta-Glucosidase Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aspergillus niger / Beta-Glucosidase Idioma: En Ano de publicação: 2022 Tipo de documento: Article