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从土壤细菌中分离并鉴定一种新型嗜热嗜碱脂肪酶

Isolation and Characterization of a New Thermoalkalophilic Lipase from Soil Bacteria.

作者信息

Rabbani Mohammad, Shafiee Fatemeh, Shayegh Zahra, MirMohammadSadeghi Hamid, Samsam Shariat Ziaedin, Etemadifar Zahra, Moazen Fatemeh

机构信息

Department of Pharmaceutical Biotechnology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Iran J Pharm Res. 2015 Summer;14(3):901-6.

Abstract

Lipases are diversified enzymes in their properties and substrate specificity, which make them attractive tools for various industrial applications. In this study, an alkalinethermostable lipase producing bacteria were isolated from soil of different regions of Isfahan province (Iran) and its lipase was purified by ammonium sulfate precipitation and ion exchange chromatography. To select a thermoalkalophil lipase producing bacterium, Rhodamine B and Horikoshi media were used and the strain that can grow at 45° Cwas selected. The isolated strain was identified using microbial and biochemical tests. One strain showed an orange colored zone on plate and grew on Horikoshi plate. Microbial and biochemical tests showed that the isolated strain was Bacillus subtilis, a Gram positive rod. In PCR, an expected band was obtained with about 371 bp. The activity of the purified lipase was 10.2 folds that of the standard enzyme using ammonium sulfate precipitation and ion exchange chromatography. The molecular weight of lipase determined by SDS-PAGE electrophoresis, was 21 and 35 KDa. Existence of two bands in SDS-PAGE electrophoresis and low amount of obtained purified enzyme highlights the necessity of optimization of purification and concentrating process.

摘要

脂肪酶在性质和底物特异性方面具有多样性,这使其成为各种工业应用中有吸引力的工具。在本研究中,从伊朗伊斯法罕省不同地区的土壤中分离出一株产碱性耐热脂肪酶的细菌,并通过硫酸铵沉淀和离子交换色谱法对其脂肪酶进行了纯化。为了筛选产嗜热嗜碱脂肪酶的细菌,使用了罗丹明B和堀越培养基,并选择了能在45℃生长的菌株。通过微生物和生化试验对分离出的菌株进行了鉴定。一株菌株在平板上显示出橙色区域,并能在堀越平板上生长。微生物和生化试验表明,分离出的菌株是枯草芽孢杆菌,一种革兰氏阳性杆菌。在PCR中,获得了一条约371 bp的预期条带。使用硫酸铵沉淀和离子交换色谱法纯化后的脂肪酶活性是标准酶的10.2倍。通过SDS-PAGE电泳测定的脂肪酶分子量为21 kDa和35 kDa。SDS-PAGE电泳中出现两条带以及获得的纯化酶量较低,凸显了优化纯化和浓缩过程的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44ab/4518119/d10b5c104b45/ijpr-14-901-g001.jpg

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