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从岩盐矿中分离出的藤黄微球菌 JPBW-1 产生并特性鉴定了一种耐卤代烃、溶剂、热的碱性脂肪酶。

Production and characterization of a halo-, solvent-, thermo-tolerant alkaline lipase by Staphylococcus arlettae JPBW-1, isolated from rock salt mine.

机构信息

Bioprocess Engineering Laboratory, Department of Biotechnology and Bioinformatics, Jaypee University of Information Technology, Waknaghat, Himachal Pradesh, 173 234, India.

出版信息

Appl Biochem Biotechnol. 2013 Nov;171(6):1429-43. doi: 10.1007/s12010-013-0433-6. Epub 2013 Aug 18.

Abstract

Studies on lipase production and characterization were carried out with a bacterial strain Staphylococcus arlettae JPBW-1 isolated from rock salt mine, Darang, HP, India. Higher lipase activity has been obtained using 10 % inoculum with 5 % of soybean oil as carbon source utilizing a pH 8.0 in 3 h at 35 °C and 100 rpm through submerged fermentation. Partially purified S. arlettae lipase has been found to be active over a broad range of temperature (30-90 °C), pH (7.0-12.0) and NaCl concentration (0-20 %). It has shown extreme stability with solvents such as benzene, xylene, n-hexane, methanol, ethanol and toluene up to 30 % (v/v). The lipase activity has been found to be inhibited by metal ions of K(+), Co(2+) and Fe (2+) and stimulated by Mn(2+), Ca(2+) and Hg(2+). Lipase activity has been diminished with denaturants, but enhanced effect has been observed with surfactants, such as Tween 80, Tween 40 and chelator EDTA. The K m and V max values were found to be 7.05 mM and 2.67 mmol/min, respectively. Thus, the lipase from S. arlettae may have considerable potential for industrial application from the perspectives of its tolerance towards industrial extreme conditions of pH, temperature, salt and solvent.

摘要

从印度哈里亚纳邦达兰的岩盐矿中分离到一株葡萄球菌(Staphylococcus arlettae JPBW-1),对其进行了脂肪酶产生和特性的研究。在 35°C、100rpm 条件下,利用 pH8.0 的环境,以 5%的大豆油为碳源,使用 10%的接种量进行深层发酵,可获得较高的脂肪酶活性。分离出的部分纯化的 S. arlettae 脂肪酶在较宽的温度(30-90°C)、pH(7.0-12.0)和 NaCl 浓度(0-20%)范围内具有活性。该脂肪酶对苯、二甲苯、正己烷、甲醇、乙醇和甲苯等溶剂具有极强的稳定性,在 30%(v/v)的浓度下仍能保持其活性。该脂肪酶的活性会被 K(+)、Co(2+) 和 Fe (2+)等金属离子抑制,而 Mn(2+)、Ca(2+) 和 Hg(2+)等金属离子则会刺激其活性。变性剂会降低脂肪酶的活性,但表面活性剂如吐温 80、吐温 40 和螯合剂 EDTA 会增强其活性。Km 和 V max 值分别为 7.05 mM 和 2.67 mmol/min。因此,从工业极端条件下的 pH、温度、盐度和溶剂耐受性的角度来看,S. arlettae 的脂肪酶可能具有很大的工业应用潜力。

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