Production of Thermostable T1 Lipase Using Agroindustrial Waste Medium Formulation

Abstract

Large-scale production of T1 lipase using conventional culture media is costly. To reduce the cost of production, an alternative growth medium using local resources has been developed. In this study, the growth of recombinant Escherichia coli and expression of T1 lipase were tested using different agroindustrial wastes as carbon and nitrogen sources by conventional method. Subsequently, by using central composite rotatable design (CCRD), a set of 30 experiments was generated to evaluate the effect of different parameters, including the amount of molasses (as carbon source), fish waste (as nitrogen source), NaCl, and inducer concentration on production of T1 lipase. Response surface methodology (RSM) analysis indicated that all factors had significant effects on T1 lipase production. This statistical analysis was utilised to develop a quadratic model to correlate various important variables for the growth of the recombinant strain and regulation of gene expression to the response (T1 lipase activity). Optimum conditions for T1 lipase production were observed to be 1.0 g/L of molasses, 2.29 g/L of fish waste, 3.46 g/L of NaCl, and 0.03 mM of IPTG (Isopropyl β-d-1-thiogalactopyranoside). Based on these conditions, the actual lipase activity was found to be 164.37 U/mL, which fitted well with the maximum predicted value of 172.89 U/mL. Therefore, the results demonstrated that, the statistical analysis, performed using RSM, was efficient in optimising T1 lipase production. Moreover, the optimum conditions obtained can be applied to scale up the process and minimise the cost of enzyme production.

Lipase Production by Solid-State Cultivation of Thermomyces Lanuginosus on By-Products from Cold-Pressing Oil Production

“…As mentioned in the introduction, lipases can catalyze reactions of hydrolysis, esterification, and transesterification [1,2]. Since the excess of water in the process favors hydrolyses [27], the process was performed at a water content of 8%(w/w) that minimized hydrolyses [28].…”

“…Lipases (triacylglycerol acylhydrolase EC 3.1.1.3) are comprised of a large group of enzymes that differ in substrate specificity and regioselectivity. They can catalyze reactions of hydrolysis, esterification, and transesterification, and exhibit the catalytic activity under mild process conditions, which has an impact on the reduction of energy consumption [1,2]. In the terms of regioselectivity, lipases can be divided into three groups: (a) Sn-1,3-specific: Hydrolyze ester bonds at position sn-1 and sn-3; (b) Sn-2-specific: Hydrolyze ester bond at position sn-2.…”

Advances in Recombinant Lipases: Production, Engineering, Immobilization and Application in the Pharmaceutical Industry

“…The use of low-cost components, mainly agro-industrial wastes, for recombinant lipase production could be a good alternative to decrease lipase production costs. Nooh et al [64] optimized the production of a lipase from Geobacillus sp. in E. coli after cultivation in low cost substrates using RSM.…”