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Item Evaluation of feeding strategies for enhanced cell-associated tannase production by serratia ficaria dtc(CAFET INNOVA Technical Society 1-2-18/103, Mohini Mansion, Gagan Mahal Road, Domalguda, Hyderabad 500029, 2011) Belur, P.D.; Goudar, D.C.Batch studies on Cell-associated tannase production showed 2.6 U/L activity in the declining phase of growth in the bioreactor. It was observed that Cell-associated tannase production under declining phase was depending upon the bacterial biomass produced under exponential phase and gallic acid level. The peak production of enzyme was always accompanied by a sharp rise in dissolved oxygen concentration. Based on these observations, fed batch fermentation by feeding a mixture of nutrients (glucose and tryptose) and Dissolved oxygen (DO) based feeding strategy of gallic acid were designed. Nutrient feeding strategy showed 10 U/L of enzyme activity at 14th h of fermentation. DO based feeding strategy of gallic acid resulted in the production of 14.4 U/L enzyme activity in the 12th h of fermentation. The enzyme production rate of 1.2 U/L.h achieved in this mode was 4.6–fold greater than the values observed in batch process and 1.68 fold greater than the productivity achieved by feeding nutrients. Hence, DO based feeding strategy of gallic acid was proved to be an effective strategy for enhanced cell-associated tannase production by Serratia ficaria DTC. © 2011 CAFET-INNOVA TECHNICAL SOCIETY. All rights reserved.Item Production of propyl gallate in nonaqueous medium using cell-associated tannase of Bacillus massiliensis: Effect of various parameters and statistical optimization(2013) Aithal, M.; Belur, P.D.Enzymatic synthesis of propyl gallate in an organic solvent was studied using cell-associated tannase (E.C. 3.1.1.20) of Bacillus massiliensis. Lyophilized biomass showing tannase activity was used as a biocatalyst. The influence of buffer pH and strength, water activity, temperature, biocatalyst loading, gallic acid concentration, and 1-propanol concentration was studied by the one-factor-at-a-time method. Subsequently, response surface methodology was applied based on a central composite design to determine the effects of three independent variables (biocatalyst loading, gallic acid concentration, and 1-propanol concentration) and their mutual interactions. A total of 20 experiments were conducted, and a statistical model was developed, which predicted the maximum propyl gallate yield of 20.28 ?g/mL in the reaction mixture comprising 40.4 mg biocatalyst, 0.4 mM gallic acid, and 6.52 % (v/v) 1-propanol in 9.5 mL benzene at 30°C. The subsequent verification experiments established the validity of the model. Under optimal conditions, 25% conversion of gallic acid to propyl gallate was achieved on a molar basis. The absence of the need for enzyme purification and subsequent immobilization steps and good conversion efficiency makes this enzyme system an interesting one. Reports on the applications of bacterial whole cell systems for synthetic reactions in organic solvents are scarce, and perhaps this is the first report on bacterial cell-associated tannase-mediated esterification in a nonaqueous medium. © 2013 International Union of Biochemistry and Molecular Biology, Inc.Item Enhancing gallic acid content in green tea extract by using novel cell-associated tannase of Bacillus massiliensis(2013) Palabhanvi, B.; Belur, P.D.Gallic acid content in green tea extract was enhanced by using a novel cell-associated tannase of Bacillus massiliensis. Biomass that contains tannase was used for this study. The activity of the cell-associated tannase was stable during 1 week of storage in the refrigerator. Response surface methodology was applied based on central composite design to determine the effects of three independent variables (pH, temperature and incubation time) and their mutual interactions. A total of 16 experiments were conducted; and a statistical model was developed, which predicted 475.74mg/L gallic acid production at pH6.2, 36C and incubation period of 16.71h. The subsequent verification experiments confirmed the validity of the model. Under optimal conditions, 84.7% of the total hydrolyzable tannins were converted to gallic acid and glucose. This naturally immobilized tannase was stable enough to be used for up to 12 runs. Practical Applications: The current study shows that naturally immobilized tannase of Bacillus massiliensis can be used instead of artificially immobilized tannase. Such naturally immobilized tannase has many advantages as it avoids expensive and laborious isolation, purification and immobilization. Ease of separation of cell-associated enzyme from the reaction mixture and absence of any detectable extracellular tannase activity after enzymatic treatment are some of the encouraging facts. Stability during storage up to 7 days, 85% tannic acid hydrolyzing efficiency, activity at pH3.5-8.0 and operational stability for 12 runs are some of the interesting features of this naturally immobilized enzyme. However, its application for tea treatment will be limited until Bacillus massiliensis gets "Generally Recognized As Safe" status. It can be employed, however, for production of gallic acid from agro residues and production of propyl gallate. © 2012 Wiley Periodicals, Inc.