Overproduction of a γ-glutamyltranspeptidase from Bacillus amyloliquefaciens in Bacillus subtilis through medium optimization
- Authors
- Cho, H.-B.; Kumar, Roy J.; Park, W.-J.; Jeon, B.-O.; Kim, Y.-W.
- Issue Date
- 2017
- Publisher
- Korean Society of Food Science and Technology
- Keywords
- Bacillus subtilis; Dual-promoter system; Medium optimization; Γ-glutamyltranspeptidase
- Citation
- Korean Journal of Food Science and Technology, v.49, no.6, pp.610 - 616
- Indexed
- SCOPUS
KCI
- Journal Title
- Korean Journal of Food Science and Technology
- Volume
- 49
- Number
- 6
- Start Page
- 610
- End Page
- 616
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/86092
- DOI
- 10.9721/KJFST.2017.49.6.610
- ISSN
- 0367-6293
- Abstract
- γ-Glutamyltranspeptidase (GGT, EC 2.3.2.2) transfers γ-glutamyl moiety from glutamine to amino acids or peptides and hydrolyzes glutamine to glutamate and ammonia. In order to overproduce γ-glutamyltranspeptidase from Bacillus amyloliquefaciens (BAGGT), the encoding gene was cloned and expressed in Bacillus subtilis. The productivity of BAGGT in Bacillus subtilis was improved by 42-fold by using a dual-promoter system that was generated by combining promoters from B. subtilis α-amylase and BAGGT genes. Through optimization of medium composition by Plackett-Burman design and central composition design, BAGGT was produced at 18.3×107 U/L of culture in the optimized medium. Compared to previously used Luria-Bertani medium, the optimized culture medium (15 g/L molasses, 60 g/L corn steep liquor, 6 g/L yeast extract, 4 g/L NaCl, 6 g/L K2HPO4, and 2 g/L KH2PO4), resulted in a 4.3-fold increase in production of BAGGT. © The Korean Society of Food Science and Technology.
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