ISSN: 0973-7510

E-ISSN: 2581-690X

Huan-Jing Zhou1,2, La-Ping He3,4 , Huan Wang1,2, Yi-Ming Zhang1, Cui-Qin Li2, Li Chen2 and Meng-Yu Chen2
1Guizhou Province Key Laboratory of Fermentation Engineering and Biopharmacy,
Guiyang 550025, China.
2School of Chemistry and Chemical Engineering, Guizhou University, Guiyang 550025, China.
3College of Life Sciences, Guizhou University, Guiyang 550025, China.
4Key Laboratory of Agricultural and Animal Products, Store & Processing of Guizhou Province, Guiyang 550025, China.
J Pure Appl Microbiol. 2014;8(3):1853-1856
© The Author(s). 2014
Received: 10/06/2013 | Accepted: 15/08/2013 | Published: 31/06/2014
Abstract

The main purpose of the work was to screen intracellular lipase-producing microbial with high selective synthesis of 1,3-diolein, a healthy lipid. The screening model is a combination of Rhodamine B-olive oil agar plat, para-nitrophenyl palmitate (r-NPP) for ester synthetase activity and HPLC analysis of products of glycerolysis of triolein. The results show that the strain GZUF36 (CCTCC No. M2012538) can be used to catalyze the selective synthesis of 1,3-diolein. 1,3-Diolein yield is 11.12% (w/w) by whole-cell of GZUF36 catalyzed glycerolysis and it is accounted for 72% of total diolein (including 1,3- and 1,2-isomer). Then, GZUF36 was identified as Aspergillus niger by morphology and 18S rDNA sequence analysis. It is also suggested that the model can be applied to screen other lipases with high ester synthetase activities.

Keywords

Aspergillus niger, 1,3-diolein, Identification, Intracellular lipase, Screening

Article Metrics

Article View: 784

Share This Article

© The Author(s) 2014. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License which permits unrestricted use, sharing, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.