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Updated: Apr 20, 2026

Generic Protocol for Optimization of Heterologous Protein Production Using Automated Microbioreactor Technology
Published on: December 15, 2017
Harnessing Bacillus inaquosorum AGSP2 for enhancing ω-transaminase production through classical and AI-supported
Shreya Pandya1, Urvish Chhaya2, Akshaya Gupte3
1Department of Microbiology, Natubhai V. Patel College of Pure and Applied Sciences, The Charutar Vidya Mandal (CVM) University, Anand, Vallabh Vidyanagar, Gujarat, 388120, India.
Abstract:
The synthesis of chiral amines is crucial since they are a key component in nearly 40% of top-selling drugs. ω-transaminases are promising biocatalysts for producing these chiral amines. This study reports the isolation of a wild-type Bacillus strain (Bacillus inaquosorum AGSP2) from a contaminated site at the Amlakhadi river, Gujarat, India. We optimized ω-transaminase production using both One Factor at a Time and Response Surface Methodology- Central Composite Design (RSM-CCD) techniques, with further model validation via an Artificial Intelligence (AI) tool, Support Vector Machine. The optimal medium, called Modified Luria-Bertani, contains fructose (12 g/L), NaCl (7.5 g/L), yeast extract (7.5 g/L), peptone (12 g/L), and α-methylbenzylamine (5 mM). Optimization increased ω-transaminase production 2.8 times, reaching an activity of 6121.88 ± 42 U/ml at 37 °C, pH 7, 120 rpm, with 2% (v/v) inoculum. The RSM-CCD model had R2 = 0.95, predicted R2 = 0.78, RMSE = 0.2327, while SVM achieved R2 = 0.99, predicted R2 = 0.96, RMSE = 0.1327. AGSP2 catalyzed the biotransformation of acetophenone with (S)-α-methylbenzylamine, resulting in a 53.32% conversion rate. These findings demonstrate the potential of combining statistical and AI tools to improve biocatalyst production and applications, presenting a sustainable approach for chiral amine synthesis and highlighting ω-transaminase's role in green biocatalysis.
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