Sharma Pushpinder, Sharma Nivedita, Pathania Shruti, Handa Shweta
University of Horticulture and Forestry, Nauni, Solan, HP 173230, India.
J Genet Eng Biotechnol. 2017 Dec;15(2):369-377. doi: 10.1016/j.jgeb.2017.06.007. Epub 2017 Jun 28.
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.
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。