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PS3在深层发酵条件下对脂肪酶的纯化、表征及其在洗涤剂工业中的应用

Purification and characterization of lipase by PS3 under submerged fermentation and its application in detergent industry.

作者信息

Sharma Pushpinder, Sharma Nivedita, Pathania Shruti, Handa Shweta

机构信息

University of Horticulture and Forestry, Nauni, Solan, HP 173230, India.

出版信息

J Genet Eng Biotechnol. 2017 Dec;15(2):369-377. doi: 10.1016/j.jgeb.2017.06.007. Epub 2017 Jun 28.

Abstract

Lipase production bacterial isolate was isolated from soil of service station and identified as PS3 by 16SrRNA with accession number |LN999829.1|. Lipase enzyme was purified by sequential methods of ammonium sulfate precipitation and Sephadex G-100 gel column chromatography. The molecular weight of purified enzyme was 31.40 kDa on SDS-PAGE. This purification procedure resulted in 2.90-fold purification of lipase with a 24.10% final yield. The purified lipase presented maximal hydrolytic activity at a temperature of 55 C, and pH of 7.0. Lipase activity was stimulated by Triton X-100 and SDS with Mg and Ca metals employ a positive effect and outlast its stable in organic solvent i.e. methanol and ethanol.

摘要

从服务站土壤中分离出产生脂肪酶的细菌菌株,并通过16SrRNA鉴定为PS3,登录号为|LN999829.1|。通过硫酸铵沉淀和Sephadex G-100凝胶柱色谱的连续方法纯化脂肪酶。在SDS-PAGE上纯化酶的分子量为31.40 kDa。该纯化程序使脂肪酶纯化了2.90倍,最终产率为24.10%。纯化的脂肪酶在55℃温度和7.0 pH下呈现最大水解活性。Triton X-100和SDS对脂肪酶活性有刺激作用,镁和钙金属有积极影响,并且在有机溶剂即甲醇和乙醇中比其稳定时间更长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c39e/6296573/a5dfe789ab00/gr5.jpg

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