Author/Authors :
Soleymani, Safoura Department of Pharmaceutical Biotechnology - Isfahan Pharmaceutical Sciences Research Center - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan, Iran , Alizadeh, Houri Department of Pharmaceutical Biotechnology - Isfahan Pharmaceutical Sciences Research Center - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan, Iran , Mohammadian, Hossein Department of Pharmaceutical Biotechnology - Isfahan Pharmaceutical Sciences Research Center - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan, Iran , Rabbani, Emad Department of Biology - Faculty of Basic Sciences - University of Isfahan, Isfahan, Iran , Moazen, Fatemeh Department of Pharmaceutical Biotechnology - Isfahan Pharmaceutical Sciences Research Center - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan, Iran , MirMohammad Sadeghi, Hamid Department of Pharmaceutical Biotechnology - Isfahan Pharmaceutical Sciences Research Center - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan, Iran , Samsam Shariat, Ziaedin Department of Biochemistry - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan, Iran , Etemadifar, Zahra Department of Biology - Faculty of Basic Sciences - University of Isfahan, Isfahan, Iran , Rabbani, Mohammed Department of Pharmaceutical Biotechnology - Isfahan Pharmaceutical Sciences Research Center - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan, Iran
Abstract :
Background: Lipase enzymes have applications in a wide range of industries. A crucial
determining factor of industrial prices of these enzymes is the culture media composition
that is constantly under review by researchers. In this work, for maximum lipase
production by Bacillus sp. ZR-5, culture media compositions were optimized using
"one variable at a time" strategy.
Methods: For this purpose, the culture medium parameters such as low and high cost
carbon and nitrogen sources, substrates and incubation times were evaluated.
Results: Maximum lipase activity was achieved after 24 hr of incubation with 1.5% of
glucose syrup (1600±69.1 u/mg), 1% of fish powder (1238±36.7 u/mg) and olive oil
(1407±2.1 u/mg) as low cost carbon and nitrogen sources and substrate, respectively.
Conclusion: Our results show a significant increase in lipase activity with usage of low
cost sources; this could help in reducing the media prices for industrial application of
lipase enzyme.