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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Liquid-liquid extraction of lipase produced by psychrotrophic yeast Leucosporidium scottii L117 using aqueous two-phase systems

Texto completo
Autor(es):
Fernandes Duarte, Alysson Wagner [1, 2] ; Lopes, Andre Moreni [3] ; Dutra Molino, Joao Vitor [3] ; Pessoa, Adalberto [3] ; Sette, Lara Duraes [1, 2, 4]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Campinas State Univ UNICAMP, Div Microbial Resources, Chem Biol & Agr Pluridisciplinary Res Ctr CPQBA, BR-13148218 Paulinia, SP - Brazil
[2] Biotechnol Interunit Postgrad Program USP IPT But, Sao Paulo, SP - Brazil
[3] Univ Sao Paulo, Sch Pharmaceut Sci, Dept Biochem & Pharmaceut Technol, BR-05508 Sao Paulo - Brazil
[4] Univ Sao Paulo State UNESP Rio Claro, Dept Biochem & Microbiol, Sao Paulo, SP - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: Separation and Purification Technology; v. 156, n. 2, p. 215-225, DEC 17 2015.
Citações Web of Science: 10
Resumo

Aqueous two-phase systems (ATPS) have been used in biomolecules separation and as an efficient alternative to traditional purification systems for lipases extraction. Here, we investigated the partitioning and recovery of lipase derived from Leucosporidium scottii L117 using ATPS and aqueous two-phase micellar systems (ATPMS). Thus, we evaluated three ATPS: (i) polyethylene glycol (PEG)/phosphate salts and (ii) PEG/polyacrylic acid (NaPA) in different molecular weights (1500, 4000 and 8000 g/mol). (iii) Triton X-114 (TX-114)/McIlvaine buffer pH 7.0 in different conditions (2.0% (w/w) of TX-114 at 25.0 and 28.0 degrees C). The PEG/phosphate and PEG/NaPA systems resulted in a great loss of enzymatic activity; thus these systems do not represent viable alternatives for these lipase extraction. The micellar systems yielded the best results for lipase extraction with enzyme activity balances ranging between 84.7% and 113.05%. After optimizing the micellar system by experimental design of the partition coefficient of lipase increased by 10.3-fold (0.75-7.76). Lipase preferentially partitioned into the micelle-rich phase with K-Lip = 7.76, % RECBot = 93.85% and PF = 1.2 at 25.03 degrees C, 5.1 pH and 10.38% TX-114 and K-Lip, = 4.77, % RECBot = 73.53% and PF = 1.97 at 28.00 degrees C, 4.5 pH and 8.0% TX-114, indicating that the ATPMS represents an alternative to purification/extraction of lipase L scottii L117. A crude lipase extract was also evaluated to define the optimum pH and temperature. Lipase reached optimal activity at 40 degrees C, and remained stable in pH values ranging from pH 3.0 to 8.0 and temperatures from 20.0 to 45.0 degrees C, with relative residual lipase activity above 80% after 30 min of incubation. (C) 2015 Elsevier B.V. All rights reserved. (AU)

Processo FAPESP: 10/17033-0 - Exploração biotecnológica de fungos derivados da Antártica
Beneficiário:Lara Durães Sette
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 13/19486-0 - Biotecnologia marinha e Antártica: enzimas microbianas e suas aplicações
Beneficiário:Lara Durães Sette
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 10/08352-5 - Biodiversidade de leveduras derivadas de ecossistemas Antárticos marinhos e terrestres e prospecção de lipases
Beneficiário:Alysson Wagner Fernandes Duarte
Modalidade de apoio: Bolsas no Brasil - Doutorado