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基于聚合酶链反应扩增从土壤中分离出二十碳五烯酸产生真菌。

Isolation of eicosapentaenoic acid-producing fungi from soil based on polymerase chain reaction amplification.

机构信息

Key Laboratory of Molecular Biophysics, Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

Z Naturforsch C J Biosci. 2011 Jul-Aug;66(7-8):429-33. doi: 10.1515/znc-2011-7-816.

Abstract

A method was developed for rapid screening and isolation of eicosapentaenoic acid (EPA)-producing soil fungi through polymerase chain reaction (PCR) amplification. Genes coding for delta6 fatty acid desaturase and delta5 fatty acid desaturase were used as molecular markers for screening these EPA-producing fungi from soil. Three out of 65 soil fungi gave positive results through PCR amplification. Two out of these three strains were found to produce EPA when they had grown in 80 ml potato/dextrose liquid medium at (25 +/- 1) degrees C for 144 h. The EPA yields were 215.81 mg 1(-1) and 263.80 mg 1(-1), respectively. The other positive strain was detected to produce arachidonic acid (AA). This study indicates that molecular detection of genes encoding delta6 and delta5 desaturases is an efficient method for primary screening of EPA- or its related polyunsaturated fatty acids (PuFAs)-producing fungi, which can improve the screening efficiency prominently.

摘要

建立了一种通过聚合酶链反应(PCR)扩增快速筛选和分离二十碳五烯酸(EPA)产生土壤真菌的方法。使用编码 delta6 脂肪酸去饱和酶和 delta5 脂肪酸去饱和酶的基因作为分子标记,从土壤中筛选这些 EPA 产生真菌。从 65 株土壤真菌中有 3 株通过 PCR 扩增得到阳性结果。这 3 株菌中有 2 株在(25 +/- 1)℃下于 80 ml 土豆/葡萄糖液体培养基中生长 144 h 时产生 EPA,产量分别为 215.81 mg/L 和 263.80 mg/L。另一个阳性菌株被检测到产生花生四烯酸(AA)。本研究表明,编码 delta6 和 delta5 去饱和酶的基因的分子检测是筛选 EPA 或其相关多不饱和脂肪酸(PUFAs)产生真菌的有效方法,可显著提高筛选效率。

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