| Literature DB >> 33502625 |
Se-Woong Park1, Byung-Ha Kang1, Hyeong-Min Lee1, Sung-Jun Lee1, Han-Seul Kim1, Hye-Won Choi1, Tae Jung Park2, Kwang-Hoon Kong3.
Abstract
The sweet-tasting protein brazzein offers considerable potential as a functional sweetener with antioxidant, anti-inflammatory, and anti-allergic properties. Here, we optimized a chemically defined medium to produce secretory recombinant brazzein in Kluyveromyces lactis, with applications in mass production. Compositions of defined media were investigated for two phases of fermentation: the first phase for cell growth, and the second for maximum brazzein secretory production. Secretory brazzein expressed in the optimized defined medium exhibited higher purity than in the complex medium; purification was by ultrafiltration using a molecular weight cutoff, yielding approximately 107 mg L-1. Moreover, the total media cost in this defined medium system was approximately 11% of that in the optimized complex medium to generate equal amounts of brazzein. Therefore, the K. lactis expression system is useful for mass-producing recombinant brazzein with high purity and yield at low production cost and indicates a promising potential for applications in the food industry.Entities:
Keywords: Brazzein; Chemically defined medium; Optimization of expression conditions; Sweet-tasting protein
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Year: 2021 PMID: 33502625 DOI: 10.1007/s00449-020-02499-y
Source DB: PubMed Journal: Bioprocess Biosyst Eng ISSN: 1615-7591 Impact factor: 3.210