期刊
MICROBIAL CELL FACTORIES
卷 17, 期 -, 页码 -出版社
BMC
DOI: 10.1186/s12934-018-0968-x
关键词
Biosurfactants; Lipopeptides; Pseudofactin; Production optimization; Pseudomonas; Design of experiments
资金
- National Science Centre, Poland [2016/20/T/NZ1/00536, 2016/21/N/NZ1/02829]
- Leading National Research Center (KNOW) program of the Wroclaw Center of Biotechnology for the years 2014-2018
- European Union
- French Region of Hauts-de-France
- ERASMUS program 2014-2020 [KA-1]
Background: Lipopeptides are a promising group of surface-active compounds of microbial origin (biosurfactants). These diverse molecules are produced mainly by Bacillus and Pseudomonas strains. Because of their attractive physiochemical and biological properties, biosurfactants are considered to be green and versatile molecules of the future. The main obstacles in widespread use of biosurfactants are mainly their low yields and high production costs. Pseudofactin (PF) is a lipopeptide produced by Pseudomonas fluorescens BD5. Recently, we identified two analogues, PF1 (C-16-Val) and PF2 (C-16-Leu), and reported that PF2 has good emulsification and foaming activities, as well as antibacterial, antifungal, anticancer, and antiadhesive properties. Reported production of PF in a mineral salt medium was approximately 10 mg/L. Results: Here, we report successful high-throughput optimization of culture medium and conditions for efficient PF production using P fluorescens BD5. Compared with production in minimal medium, PF yield increased almost 120-fold, up to 1187 +/- 13.0 mg/L. Using Plackett Burman and central composite design methodologies we identified critical factors that are important for efficient PF production, mainly high glycerol concentration, supplementation with amino acids (leucine or valine) and complex additives (e.g. tryptone), as well as high culture aeration. We also detected the shift in a ratio of produced PF analogues in response to supplementation with different amino acids. Leucine strongly induces PF2 production, while valine addition supports PF1 production. We also reported the identification of two new PF analogues: PF3 (C-18-Val) and PF4 (C-18-Leu). Conclusions: Identification of critical culture parameters that are important for lipopeptide production and their high yields can result in reduction of the production costs of these molecules. This may lead to the industrial-scale production of biosurfactants and their widespread use. Moreover, we produced new lipopeptide pure analogues that can be used to investigate the relationship between the structure and biological activity of lipopeptides.
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