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Application of Factorial Experimental Designs for Optimization of Cyclosporin A Production by Tolypocladium inflatum in Submerged Culture  

Abdel-Fattah, Y.R. (Bioprocess Development Department, Genetic Engineering and Biotechnology Research Institute, Mubarak City for Scientific Research and Technology Applications)
Enshasy, H. El (Bioprocess Development Department, Genetic Engineering and Biotechnology Research Institute, Mubarak City for Scientific Research and Technology Applications)
Anwar, M. (Microbiology Department, Faculty of Pharmacy, Alexandria University)
Omar, H. (Microbiology Department, Faculty of Pharmacy, Alexandria University)
Abolmagd, E. (Bioprocess Development Department, Genetic Engineering and Biotechnology Research Institute, Mubarak City for Scientific Research and Technology Applications)
Publication Information
Journal of Microbiology and Biotechnology / v.17, no.12, 2007 , pp. 1930-1936 More about this Journal
Abstract
A sequential optimization strategy based on statistical experimental designs was employed to enhance the production of cyclosporin A (CyA) by Tolypocladium inflatum DSMZ 915 in a submerged culture. A 2-level Plackett-Burman design was used to screen the bioprocess parameters significantly influencing CyA production. Among the 11 variables tested, sucrose, ammonium sulfate, and soluble starch were selected, owing to their significant positive effect on CyA production. A response surface methodology (RSM) involving a 3-level Box-Behnken design was adopted to acquire the best process conditions. Thus, a polynomial model was created to correlate the relationship between the three variables and the CyA yield, and the optimal combination of the major media constituents for cyclosporin A production, evaluated using the nonlinear optimization algorithm of EXCEL-Solver, was as follows (g/l): sucrose, 20; starch, 20; and ammonium sulfate, 10. The predicted optimum CyA yield was 113 mg/l, which was 2-fold the amount obtained with the basal medium. Experimental verification of the predicted model resulted in a CyA yield of 110 mg/l, representing 97% of the theoretically calculated yield.
Keywords
Cyclosporin A; Tolypocladium inflatum; optimization; factorial designs;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
Times Cited By Web Of Science : 8  (Related Records In Web of Science)
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1 Bernard, J. 1986. Cyclosporin: foreward. Prog. Allergy 38: 1-8
2 Dreyfuss, M., E. Härri, H. Hofmann, H. Kobel, W. Pache, and H. Tscherter. 1976. Cyclosporin A and C. New metabolites from Trichoderma polysporum. Eur. J. Appl. Microbiol. 3: 125-133   DOI
3 Plackett, R. L. and J. P. Burman. 1946. The design of optimum multi-factorial experiments. Biometrika 33: 305-325   DOI   ScienceOn
4 Sekar, C. and K. Balaraman. 1998a. Optimization studies on the production of cyclosporin A by solid state fermentation. Bioprocess Eng. 18: 293-296   DOI   ScienceOn
5 Zocher, R., T. Nihira, E. Paul, N. Madry, H. Peeters, H. Kleinkauf, and U. Keller. 1986. Biosynthesis of cyclosporin A: Partial purification and properties of a multifunctional enzyme from Tolypocladium matum. Biochemistry 25: 550-553   DOI   ScienceOn
6 Dittmann, J., R. W. Wenger, H. Kleinkauf, and A. Lawen. 1994. Mechanism of cyclosporin A biosynthesis: Evidence for synthesis via a single linear undecapeptide precursor. J. Biol. Chem. 269: 2841-2846
7 Abdel-Fattah, Y. R. and A. A. Gaballa. 2006. Synthesis of DNA ladder by polymerase chain reaction and optimization of yield using response surface methodology. Biotechnology 5: 166- 172   DOI
8 Rehacek, Z. and Z. De-xiu. 1991. The biochemistry of cyclosporin formation: A review. Process Biochem. 26: 157-166   DOI   ScienceOn
9 Sekar, C. and K. Balaraman. 1998b. Immobilization of the fungus, Tolypocladium sp. for the production of cyclosporin A. Bioprocess Eng. 19: 281-283
10 Murthy, M. V., E. V. Mohand, and A. K. Sadhukhan. 1999. Cyclosporin-A production by Tolypocladium inflatum using solid state fermentation. Process Biochem. 34: 269-280   DOI   ScienceOn
11 Weber, G., K. Schorgendorfer, E. Schneider-Scherzer, and E. Leitner. 1994. The peptide synthetase catalyzing cyclosporine production in Tolypocladium niveum is encoded by a giant 45.8-kilobase open reading frame. Curr. Genet. 26: 120-125   DOI   ScienceOn
12 Abdel-Fattah, Y. R., H. M. Saeed, Y. M. Gohar, and M. A. El-Baz. 2005. Improved production of Pseudomonas aeruginosa uricase by optimization of process parameters through statistical experimental designs. Proc. Biochem. 40: 1707-1714
13 Demain, A., Y. Aharonowitz, and J. Martin. 1983. Metabolic control of secondary metabolic pathways. In: L. Vining (ed.), Biochemistry and Genetics of Commercially Important Antibiotics, Ch. 3. Addison-Wesley, Reading, MA
14 Sanket, J., S. Yadav, A. Nerurkar, and A. J. Desai. 2007. Statistical optimization of medium components for the production of biosurfactant by Bacillus lichenifirmis K51. J. Microbiol. Biotechnol. 17: 313-319   과학기술학회마을
15 Kobel, H. and R. Traber. 1982. Directed biosynthesis of cyclosporins. Eur. J. Appl. Microbiol. Biotechnol. 14: 237-240   DOI
16 Billich, A. and R. Zocher. 1987. Enzymatic synthesis of cyclosporin A. J. Biol. Chem. 262: 17258-17259
17 Agathos, S. N., J. W. Marshall, C. Moraiti, R. Parekh, and C. Madhosingh. 1986. Physiological and genetic factors for process development of cyclosporin fermentations. J. Ind. Microbiol. 1: 39-48   DOI
18 Lawen, A. and R. Zocher. 1990. Cyclosporin synthetase, the most complex peptide synthesizing multienzyme so far described. J. Biol. Chem. 265: 11355-11360
19 Dubois, M., K. Gilles, J. Hamilton, P. Rebers, and F. Smith. 1956. Colorimetric method of determination of sugars and related substances. Anal. Chem. 290: 181-186
20 Wenger, R. M. 1984. Synthesis of cyclosporin. Helv. Chim. Acta 67: 502-506   DOI
21 Box, G. E. P. and D. W. Behnken. 1960. Some new three level designs for the study of quantitative variables. Technometrics 2: 455-475   DOI   ScienceOn
22 Park, N. S., J. S. Myeong, H.-J. Park, K. Han, S.-N. Kim, and E.-S. Kim. 2005. Characterization and culture optimization of regiospecific cyclosporin hydroxylation in rare actinomycetes species. J. Microbiol. Biotechnol. 15: 188-191   과학기술학회마을
23 Kreuzig, F. 1984. High speed liquid chromatography with conventional instruments for determination of cyclosporin A, B, C, and D in fermentation broth. J. Chromatogr. 290: 181-186   DOI
24 Strobel, R. and G. Sullivan. 1999. Experimental design for improvement of fermentations, pp. 80-93. In: A. L. Demain and J. E. Davies (eds.), Manual of Industrial Microbiology and Biotechnology. Washington, ASM Press
25 Weber, G. and E. Leitner. 1994. Disruption of the cyclosporin synthetase gene of Tolypocladium niveum. Curr. Genet. 26: 461-467   DOI   ScienceOn