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Environmental chitinous materials as adsorbents for one-step purification of protease and chitosanase

机译:环境几丁质材料作为吸附剂,可一步纯化蛋白酶和壳聚糖酶

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We describe the use of chitinous materials as adsorbents for purification of protease and chitosanase from bromelain solution and chitosanase from culture supernatants of three bacterial strains: Serratia marcescens TKU011, Bacillus cereus TKU022 and Acinetobacter calcoaceticus TKU024. The best adsorption results were observed when crude shrimp shell chitin (CSSC) and 750-nm chitin nanoparticles (CNP) were used. The optimum temperatures for protease adsorption from bromelain solution (22.9 mg/mL) by CSSC (0.1 g) and by 750-nm CNP (0.1 g) were 4 and 25 ℃, respectively. The purification folds of bromelain by CSSC and 750-nm CNP were 5.2 and 4.5, respectively. For purification of protease from culture supernatants of TKU011, 750-nm CNP was 4.0-fold better than CSSC. However, CSSC exhibited purification folds of 2.9 and 3.3 for the chitosanases from TKU022 and TKU024, respectively. The adsorbed chitinolytic enzymes TKU015 chitinase (30 kDa) and TKU024 chitosanase (27 kDa) exhibited high purity by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). Thus, CSSC and 750-nm CNP indicate potential for use as tools for one-step purification of bacterial chitinolytic enzymes from culture supernatants.
机译:我们描述了使用几丁质材料作为吸附剂,从菠萝蛋白酶溶液中纯化蛋白酶和壳聚糖酶,以及从三种细菌菌株:粘质沙雷氏菌TKU011,蜡状芽孢杆菌TKU022和钙不动杆菌TKU024的培养上清液中纯化壳聚糖酶。当使用粗虾壳甲壳质(CSSC)和750 nm甲壳质纳米颗粒(CNP)时,观察到最佳吸附效果。 CSSC(0.1 g)和750 nm CNP(0.1 g)从菠萝蛋白酶溶液(22.9 mg / mL)吸附蛋白酶的最佳温度分别为4和25℃。 CSSC和750 nm CNP对菠萝蛋白酶的纯化倍数分别为5.2和4.5。为了从TKU011的培养上清液中纯化蛋白酶,750 nm CNP比CSSC强4.0倍。但是,CSSC对来自TKU022和TKU024的壳聚糖酶分别显示出2.9和3.3的纯化倍数。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE),吸附的几丁质分解酶TKU015几丁质酶(30 kDa)和TKU024几丁质酶(27 kDa)表现出高纯度。因此,CSSC和750 nm CNP表示有潜力用作从培养上清液一步纯化细菌几丁质分解酶的工具。

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