Detalhes bibliográficos
| Ano de defesa: |
2013 |
| Autor(a) principal: |
CORREIA, Patyanne Carvalho
 |
| Orientador(a): |
PORTO, Tatiana Souza |
| Banca de defesa: |
CARVALHO, Maria da Paz,
MAGALHÃES, Oliane Maria Correia,
PORTO, Camila Souza |
| Tipo de documento: |
Dissertação
|
| Tipo de acesso: |
Acesso aberto |
| Idioma: |
por |
| Instituição de defesa: |
Universidade Federal Rural de Pernambuco
|
| Programa de Pós-Graduação: |
Programa de Pós-Graduação em Biociência Animal
|
| Departamento: |
Departamento de Morfologia e Fisiologia Animal
|
| País: |
Brasil
|
| Palavras-chave em Português: |
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| Palavras-chave em Inglês: |
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| Área do conhecimento CNPq: |
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| Link de acesso: |
http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/4654
|
Resumo: |
Keratinase are proteolytic enzymes whose substrate are a group of fibers and insoluble proteins denominate keratin. Some several micro-organisms such as fungi are capable to produce keratinase and to hydrolyze disulfide bonds present in keratinous substrates. The aim of this study was to select a producer keratinase and develop an integrated system which combines production, extraction and purification of keratinase by extractive fermentation in aqueous two-phase system (ATPS), prepared with polyethylene glycol (PEG) and citrate salts. Were observed the fermentation with Aspergillus sp SIS 11 was the higher producer of keratinases (7.65 U / mL), which the best conditions for enzyme production showed feather 0.5% o and pH 9.0. An ATPS which is composed of 20% (w/w) PEG 400 molar mass (g/mol), pH 8.0, 20% (w / w) sodium citrate, provided the best conditions for extractive keratinase production. Promoting greater (purification) 7.41, partition coefficient 0.74 and enzyme recovery 503.6%. In extractive fermentation enzyme produced presented partition coefficient K = 1.39 and enzyme recovery 65.08%. The studied strain was effective for enzyme production and biotechnological potential to use in animal feed. |
