Integration of ultrafiltration into an aqueous two-phase system in the keratinase purification

被引:21
|
作者
Sala, Luisa [1 ]
Gauterio, Gabrielle Victoria [1 ]
Younan, Felipe Fares [1 ]
Brandelli, Adriano [2 ]
Moraes, Caroline Costa [3 ]
Kalil, Susana Juliano [1 ]
机构
[1] Univ Fed Rio Grande, Escola Quim & Alimentos, BR-96201900 Rio Grande, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Inst Ciencia & Tecnol Alimentos, BR-91501970 Porto Alegre, RS, Brazil
[3] Univ Fed Pampa, BR-96412420 Bage, RS, Brazil
关键词
Diafiltration; Keratin; Proteolysis; Polyethylene glycol; KERATINOLYTIC PROTEASE; ALKALINE PROTEASE; ENZYMATIC DEGRADATION; POLYETHYLENE-GLYCOL; PARTITION BEHAVIOR; 2-STEP EXTRACTION; PRION PROTEIN; PLASMID DNA; ENZYMES; SEPARATION;
D O I
10.1016/j.procbio.2014.07.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Keratinases are proteases that have several important applications in the daily life. Although they have attracted the attention of researchers in the field of biotechnology, their use in industrial processes requires efficient purification techniques allowing scaling-up. Among these techniques, the aqueous two-phase system and ultrafiltration stand out. This study reports the purification of keratinase from Bacillus sp. P45 by aqueous two-phase system two-stage process integrated to ultrafiltration. In the aqueous two-phase system, the addition of sodium chloride in polyethylene glycol-potassium phosphate system favored the partitioning of keratinase. The keratinase purified by an aqueous two-phase system two-stage process integrated to ultrafiltration in diafiltration mode presented purification factor of 6.1-fold and enzymatic recovery of 56.3%, and the enzyme was separated from polyethylene glycol. The purified keratinase was capable of hydrolyzing both soluble and insoluble protein substrates more efficiently than the crude enzyme, evidencing the beneficial effect of enzyme purification on its catalytic activity. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2016 / 2024
页数:9
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