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首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Bioremediation of waste cooking oil using a novel lipase produced by Penicillium chrysogenum SNP5 grown in solid medium containing waste grease
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Bioremediation of waste cooking oil using a novel lipase produced by Penicillium chrysogenum SNP5 grown in solid medium containing waste grease

机译:使用在含有废油脂的固体培养基中生长的产黄青霉SNP5生产的新型脂肪酶对食用油进行生物修复

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摘要

The aim of present work was to bioremediate the waste cooking oil using a novel lipase produced in solid medium containing waste grease and wheat bran by Penicillium chrysogenum. Enzyme extracted with phosphate buffer was purified 10.6 and 26.28-fold after 90% ammonium sulfate precipitation and ion-exchange chromatography, respectively. The partial characterization of enzyme revealed its K _m and V _(max) value for p-nitrophenolpamitate as 0.4mM and 47.61U/ml, respectively. The relative molecular mass of lipase was 40kDa by SDS-PAGE and confirmed by zymogram. Purified lipase was most stable at 40°C and at 8.0 pH. Lipase activity was enhanced by metal ions such as Mg ~(2+), Fe ~(2+), Ca ~(2+) and non-ionic surfactant TritonX-100, while suppressed in the presence of SDS. Crude lipase was applied on cooking oil waste and the acid value was 26.92mg/g. This showed that the enzyme could be employed for the bioremediation of used cooking oil.
机译:当前工作的目的是使用一种新的脂肪酶对废弃的食用油进行生物修复,所述的脂肪酶是在含有废油脂和麦麸的固体培养基中生产的一种新的脂肪酶。经过90%硫酸铵沉淀和离子交换色谱分离后,用磷酸盐缓冲液提取的酶分别纯化了10.6倍和26.28倍。酶的部分表征显示其对硝基苯酚氨基甲酸酯的K_m和V_(max)值分别为0.4mM和47.61U / ml。通过SDS-PAGE,脂肪酶的相对分子质量为40kDa,并通过酶谱证实。纯化的脂肪酶在40°C和8.0 pH下最稳定。诸如Mg〜(2 +),Fe〜(2 +),Ca〜(2+)和非离子表面活性剂TritonX-100等金属离子增强了脂肪酶的活性,同时在SDS的存在下被抑制。将粗脂肪酶施加到食用油废料上,酸值为26.92mg / g。这表明该酶可用于用过的食用油的生物修复。

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