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首页> 外文期刊>Biotechnology and Applied Biochemistry >Extraction protease expressed by Penicillium fellutanum from the Brazilian savanna using poly(ethylene glycol)/sodium polyacrylate/NaCl aqueous two-phase system
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Extraction protease expressed by Penicillium fellutanum from the Brazilian savanna using poly(ethylene glycol)/sodium polyacrylate/NaCl aqueous two-phase system

机译:用聚(乙二醇)/聚丙烯酸钠/ NaCl水两相体系从巴西大草原中提取落青霉表达的蛋白酶

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摘要

The partitioning of protease expressed by Penicillium fellutanum from the Brazilian savanna in a novel inexpensive and stable aqueous two-phase system (ATPS) composed of poly(ethylene glycol) (PEG) and sodium polyacrylate (NaPA) was studied in this work using factorial design. The ATPS is formed by mixing both polymers with a salt (NaCl) and fermented broth of P. fellutanum. The effects of molar mass (2,000, 4,000, and 6,000 gmol(-1)) and concentration (6, 8, and 10 wt%) of PEG and that of NaPA concentration (6, 8, and 10 wt%) on protease partitioning (K) at 25 degrees C were studied. A two-level factorial design (2(3)) was implemented. The effect of Na2SO4 concentration (5, 10, and 15 wt%) on the reextraction of the enzyme was also analyzed. The partition coefficient K ranged from 77.51 to 1.21, indicating the versatility of the method. The reextraction was achieved with the addition of 5% Na2SO4, allowing the partitioning of the protease to the upper phase, whereas total proteins were directed to the bottom phase. The results of partitioning using the PEG/NaPA/NaCl system and that of the subsequent reextraction with Na2SO4 suggest that this method can be used to purify proteases from fermented broth of P. fellutanum. (C) 2014 International Union of Biochemistry and Molecular Biology, Inc.
机译:在这项工作中,使用因子设计研究了由巴西热带稀树青霉表达的蛋白酶在由聚乙二醇(PEG)和聚丙烯酸钠(NaPA)组成的新型廉价且稳定的水两相系统(ATPS)中的分配。 。通过将两种聚合物与盐(NaCl)和腐烂假单胞菌的发酵肉汤混合,形成ATPS。摩尔质量(2,000、4,000和6,000 gmol(-1))和PEG浓度(6、8和10 wt%)和NaPA浓度(6、8和10 wt%)对蛋白酶分配的影响研究了在25摄氏度下的(K)。实施了两级因子设计(2(3))。还分析了Na2SO4浓度(5、10和15 wt%)对酶再提取的影响。分配系数K在77.51到1.21之间,表明该方法的多功能性。通过添加5%Na2SO4进行再萃取,从而使蛋白酶分配到上层相,而总蛋白则被引导到下层相。使用PEG / NaPA / NaCl系统分配的结果以及随后用Na2SO4再提取的结果表明,该方法可用于从法氏假单胞菌发酵液中纯化蛋白酶。 (C)2014国际生物化学与分子生物学联合会

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