Literature DB >> 31218179

Statistical optimization of cultural medium composition of thermoalkalophilic lipase produced by a chemically induced mutant strain of Bacillus atrophaeus FSHM2.

Atefeh Ameri1, Mojtaba Shakibaie1,2, Zahra Sahami3, Mehdi Khoobi4, Hamid Forootanfar2,5.   

Abstract

Extremophilic microbial derived lipases have been widely applied in different biotechnological processes due to their resistance to harsh conditions such as high salt concentration, elevated temperature, and extreme acidic or alkaline pH. The present study was designed to overproduce the halophilic, thermoalkalophilic lipase of Bacillus atrophaeus FSHM2 through chemically induced random mutagenesis and optimization of cultural medium components assisted by statistical experimental design. At first, improvement of lipase production ability of B. atrophaeus FSHM2 was performed through exposure of the wild bacterial strain to ethidium bromide for 5-90 min to obtain a suitable mutant of lipase producer (designated as EB-5, 4301.1 U/l). Afterwards, Plackett-Burman experimental design augmented to D-optimal design was employed to optimize medium components (olive oil, maltose, glucose, sucrose, tryptone, urea, (NH4)2SO4, NaCl, CaCl2, and ZnSO4) for lipase production by the EB-5 mutant. A maximum lipase production of 14,824.3 U/l was predicted in the optimum medium containing 5% of olive oil, 0.5% of glucose, 0.5% of sucrose, 2% of maltose, 2.5 g/l of yeast extract, 1.75 g/l of urea, 1.75 g/l of (NH4)2SO4, 2.5 g/l of tryptone, 2 g/l of NaCl, 1 g/l of CaCl2, and 1 g/l of ZnSO4. A mean value of 14,773 ± 576.9 U/l of lipase was acquired from real experiments.

Entities:  

Keywords:  Bacillus atrophaeus; Ethidium bromide; Lipase; Medium optimization; Mutagenesis

Year:  2019        PMID: 31218179      PMCID: PMC6571094          DOI: 10.1007/s13205-019-1789-2

Source DB:  PubMed          Journal:  3 Biotech        ISSN: 2190-5738            Impact factor:   2.406


  25 in total

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1.  Statistical optimization of culture conditions of mesophillic gamma-glutamyl transpeptidase from Bacillus altitudinis IHB B1644.

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