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Bacterial Peptide Display for the Selection of Novel Biotinylating Enzymes
Published on: October 3, 2019
Efficient Expression of Small Molecule Bioactive Peptides in Bacillus licheniformis
Hanchao Zhang1, Lanying Shao1, Qinghua Feng1
1Key Laboratory of Industrial Fermentation Microbiology of the Ministry of Education, College of Bioengineering, Tianjin University of Science & Technology, No. 29, 13 Main Street, Tianjin Economic and Technological Development Zone, Tianjin, 300457, PR China.
Abstract:
Stable expression of γ-Glutamyltranspeptidase (GGT)-BPC157 and mScarlet-BPC157 in Bacillus licheniformis strain 2709 by chromosomal integration. Fermentation conditions were optimized using single-factor and orthogonal experiments to maximize yield. Under optimal conditions (2% inoculum, 40 g/L soybean peptone, and 80 g/L glucose), reporter-based expression signals increased approximately threefold compared to the basal medium. The fusion proteins were purified by fractional ammonium sulfate precipitation; optimal saturations were 50% and 60%, respectively. Biological activity was assessed in a rat model of ethanol-induced acute gastric ulcer. Both proteins showed gastroprotective and therapeutic activity, with ulcer inhibition rates ranging from 75.3% to 82.9% protective regime and 80.4% to 84.6% therapeutic regime. Histological analysis showed that the treatment reduced mucosal inflammation and stimulated glandular repair. ELISA showed significant downregulation of proinflammatory cytokines TNF-α, IL-1β, and IL-6 in gastric tissue. These results suggest a biotechnological production strategy for BPC 157 and applications for gastric ulcer treatment.
