Optimization of Fermentation Medium for Producing α-Hydroxyphenylacetic Acid by Using Plackett-Burman Design and Response Surface Methodology
- 1 Collage of Chemistry and Chemical Engineering, Fuzhou University, Fujian, Fuzhou, China
- 2 Collage of Chemistry and Chemical Engineering, Fuzhou University, Fujian, Fuzhou, China
- 3 Collage of Chemistry and Chemical Engineering, Fuzhou University, Fujian, Fuzhou, China
- 4 Collage of Chemistry and Chemical Engineering, Fuzhou University, Fujian, Fuzhou, China
- 5 Collage of Chemistry and Chemical Engineering, Fuzhou University, Fujian, Fuzhou, China
- 6 Department of Chemical Engineering, University of Ottawa, Ottawa, Canada
- 7 Department of Mechanical and Aerospace Engineering, Carleton University, Ottawa, Canada
Abstract
Plackett-Burman design and response surface methodology w ere applied in order to optimize the fermentation medium of (R)-α-hydroxyphenylacetic acid ((R)-HPA) producing Bacillus sp. HZG-19. The factors playing important roles in the production of (R)-HPA were selected based on Plackett-Burman design. The path of steepest ascent was undertaken to optimize said fermentation medium. Finally, the optimal levels of the factors with the greatest change in regard to product yield were further optimized using Box-Behnken and response surface analysis. The optimal conditions were found to be as follows: casein peptone 30.49 (g × L - 1 ), glycerol 14.09 (g × L - 1 ), KH 2 PO 4 0.1345 (g × L - 1 ), K 2 HPO 4 0.01 (g × L - 1 ), CaCl 2 0.1 (g × L - 1 ), MnSO 4 0.01 (g × L -1 ). Under the optimal conditions described above, the yield of (R)-HPA reached 63.30%, which indicated an increase of 14.9%, as compared to the yield obtained before optimization.
- A. Furlenmeier, P. Quitt, K. Vogler and P. Lanz, “6-Acyl Derivatives of Aminopenicillanic Acid,” US Patent No. 3957758, 1976.
- J. Mills, K. K. Schmiegel and W. N. Shaw, “Phenethanolamines, Compositions Containing the Same, and Method for Effecting Weight Control,” US Patent No. 4391826, 1983.
- P. Saravanan and V. K. Singh, “An Efficient Synthesis of Chiral Nonracemic Diamines: Application in Asymmetric Synthesis,” Tetrahedron Letters, Vol. 39, No. 1-2, 1998, pp. 167-170. http://dx.doi.org/10.1016/S0040-4039(97)10578-0
- G. D. Yadav and P. Sivakumar, “Enzyme-Catalyzed Optical Resolution of Mandelic Acid via (RS)-Methyl Mandelate in Non-Aqueous Media,” Biochemical Engineering Journal, Vol. 19, No. 2, 2004, pp. 101-107. http://dx.doi.org/10.1016/j.bej.2003.12.004
- Y. Yamazaki and H. Maeda, “Enzymatic Synthesis of Optically Pure (r)-(-)-Mandelic Acid and Other 2-Hydroxycarbonic Acids: Screening for the Enzyme, and Its Purification, Characterization and Use,” Agricultural and Biological Chemistry, Vol. 50, No. 10, 1986, pp. 2621-2631. http://dx.doi.org/10.1271/bbb1961.50.2621
- D. A. Evans, M. M. Morrissey and R. L. Dorow, “The Asymmetric Oxygenation of Chiral Imide Enolates. A General Approach to the Synthesis of Enantiomerically Pure a-Hydroxy Carboxylic Acid Synthons,” Journal of the American Chemical Society, Vol. 107, No. 14, 1985, pp. 4346-4348. http://dx.doi.org/10.1021/ja00300a054
- S Tsuchiya, K. Miyamoto and H. Ohta, “Highly Efficient Conversion of (±)-Mandelic Acid to Its (r)-(-)-Enantiomer by Combination of Enzyme-Mediated Oxidation and Reduction,” Biotechnology Letters, Vol. 14, No. 12, 1992, pp. 1137-1142. http://dx.doi.org/10.1007/BF01027017
- E. Takahashi, K Nakamichi and M. J. Furui, “R-(-)Mandelic Acid Production from Racemic Mandelic Acids Using Pseudomonas polycolor IFO 3918 and Micrococcus freudenreichii FERM-P 13221,” Journal of Fermentation and Bioengineering, Vol. 79, No. 5, 1995, pp. 439-442. http://dx.doi.org/10.1016/0922-338X(95)91258-7
- B. Y. Kim, K. C. Hwang, H. S. Song, N. Chung and W. G. Bang, “Optical Resolution of rs-(+/-)-Mandelic Acid by Pseudomonas sp.,” Biotechnology Letters, Vol. 22, No. 23, 2000, pp. 1871-1875. http://dx.doi.org/10.1023/A:1005649908991
- E. Wehtje, P. Adlercreutz and B. Mattiasson, “Formation of C-C Bonds by Mandelonitrile Lyase in Organic Solvents,” Biotechnology and Bioengineering, Vol. 36, No. 1, 1990, pp. 39-46. http://dx.doi.org/10.1002/bit.260360106