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Isolation partial purification biochemical characterization and detergent compatibility of alkaline protease produced by Bacillus subtilis Alcaligenes faecalis and Pseudomonas aeruginosa obtained from sea water samples

机译:海水样品中枯草芽孢杆菌粪产碱菌和铜绿假单胞菌产生的碱性蛋白酶的分离部分纯化生化特性和清洁剂相容性

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摘要

In the current study, bacteria isolated from sea water samples of Murdeshwar, Karnataka, were screened for the production of alkaline protease by culturing them onto skim milk agar media. Of the isolated bacteria, Bacillus subtilis, Pseudomonas aeruginosa and Alcaligenes faecalis showed distinct zones of hydrolysis due to enzyme production. They were each inoculated into enzyme production media under submerged fermentation conditions at 37 °C for 48 h with a constant agitation of 120 rpm. Partial purification of alkaline protease was carried out by isoelectric precipitation. Enzyme activity was determined under varying conditions of pH, incubation temperature, different substrates, carbon and nitrogen sources and salt concentrations using sigma’s universal protease activity assay. Enzyme immobilization was carried out using 2% Sodium alginate and 0.1 M ice cold CaCl2 and its activity under varying pH, temperature conditions and detergent compatibility was assayed. Efficacy of enzyme in stain removal was tested and haemolysis was observed within of 60 s which resulted in removal of the stain. Among the three organisms, enzyme from Bacillus subtilis showed highest activity in all cases indicating that it was the most ideal organism for enzyme production.
机译:在当前的研究中,从卡纳塔克邦默德斯瓦尔海水样品中分离出的细菌通过在脱脂琼脂培养基上培养而筛选出碱性蛋白酶的产生。在分离的细菌中,枯草芽孢杆菌,铜绿假单胞菌和粪便产碱杆菌由于产生酶而显示出明显的水解区域。将它们分别在37°C的深层发酵条件下接种到酶生产培养基中,持续搅拌120 withrpm,持续48 h。通过等电沉淀进行碱性蛋白酶的部分纯化。使用sigma通用蛋白酶活性测定法,可以在不同的pH,孵育温度,不同的底物,碳和氮源以及盐浓度条件下确定酶的活性。用2%海藻酸钠和0.1 M冰冷的CaCl2进行酶固定,并在不同的pH,温度条件和去污剂相容性下测定其活性。测试了酶在去除污渍中的功效,并在60秒内观察到溶血作用,从而导致了污渍的去除。在这三种生物中,枯草芽孢杆菌的酶在所有情况下均表现出最高的活性,这表明它是生产酶的最理想生物。

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