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H. Abo, T. Matsumura, T. Kodama, H. Ohta, K. Fukui, K. Kato and H. Kagawa, “Peptide Sequences for Sucrose Splitting and Glucan Binding within Streptococcus sobrinus Glucosyltransferase (Water-Insoluble Glucan Synthetase),” Journal of Bacteriolology, Vol. 173, 1991, pp. 989-996.

has been cited by the following article:

• TITLE: Development of Efficient Fermentation Process at Bioreactor Level by Taguchi's Orthogonal Array Methodology for Enhanced Dextransucrase Production from Weissella confusa Cab3

  AUTHORS: Shraddha Shukla, Arun Goyal

  KEYWORDS: Lactic Acid Bacteria; Weissella confusa; Dextransucrase; Taguchi's Orthogonal Array Method; Bioreactor

  JOURNAL NAME: Advances in Microbiology, Vol.2 No.3, September 25, 2012

  ABSTRACT: The influence of medium ingredients on extracellular dextransucrase production by a new bacterial strain Weissella confusa Cab3 (Genbank Accession Number JX649223) was evaluated using fractional factorial design of Taguchi's orthogonal array. Four metabolism influencing factors viz. sucrose, yeast extract, K2HPO4 and Tween80 were selected to optimize dextransucrase production by W. confusa Cab3 using fractional factorial design of Taguchi methodology. Based on the influence of interaction components of fermentation, least significant factors of individual level have higher interaction severity index and vice versa for enzyme production from Weissella confusa Cab3. Sucrose and yeast extract were found to be the most significant factors which positively influenced the dextransucrase production. The optimized medium composition consisted of sucrose—5%; yeast extract—2%; K2HPO4—1.0%; Tween80—0.5%, based on Taguchi orthogonal array method. The optimized composition gave an experimental value of dextransucrase activity of 17.9 U/ml at shake flask level which corresponded well with the predicted value of 17.54 U/ml by the model. The optimized medium by Taguchi method gave significant (3 fold) enhancement of dextransucrase activity as compared to unoptimised enzyme activity of 6.0 U/ml. The dextransucrase production was scaled up in lab scale bioreactor resulting in further enhancement of enzyme activity (22.0 U/ml).