4.8 Article

Novel biotransformation process of podophyllotoxin to produce podophyllic acid and picropodophyllotoxin by Pseudomonas aeruginosa CCTCC AB93066, Part II: Process optimization

Journal

BIORESOURCE TECHNOLOGY
Volume 100, Issue 7, Pages 2271-2277

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biortech.2008.10.044

Keywords

Biotransformation process optimization; Podophyllotoxin; Podophyllic acid; Fed-batch biotransformation; Pseudomonas aeruginosa

Funding

  1. The National Natural Science Foundation of China (NSFC) [20706012]
  2. National High Technology Research and Development Key Program of China [2007AA021506]
  3. Hubei Provincial Innovative Research Team in University [T200608]
  4. Hubei Provincial Science Foundation for Distinguished Young Scholars [2006ABB034]
  5. Hubei Provincial International Cooperation Foundation for Scientific Research [2007CA012]
  6. Science and Technology Commission of Wuhan Municipality Chenguang Jihua [20065004116-31]
  7. Scientific Research Foundation for the Returned Overseas Chinese Scholars (Ministry of Personnel and State Education Ministry)
  8. Scientific Research Key Foundation from Hubei University of Technology [306.18002]

Ask authors/readers for more resources

This work optimized the novel biotransformation process of podophyllotoxin to produce podophyllic acid by Pseudomonas aeruginosa CCTCC AB93066. Firstly, the biotransformation process was significantly affected by medium composition. 5 g/l of yeast extract and 5 g/l of peptone were favorable for podophyllic acid production (i.e. 25.3 +/- 3.7 mg/l), while not beneficial for the cell growth of P. aeruginosa. This indicated that the accumulation of podophyllic acid was not corresponded well to the cell growth of P. aeruginosa. 0 g/l of sucrose was beneficial for podophyllic acid production (i.e. 34.3 +/- 3.9 mg/l), which led to high podophyllotoxin conversion (i.e. 98.2 +/- 0.1%). 1 g/l of NaCl was the best for podophyllic acid production (i.e. 47.6 +/- 4.0 mg/l). Secondly, the production of podophyllic acid was significantly enhanced by fed-batch biotransformation. When each 100 mg/l of podophyllotoxin was added to the biotransformation system after 4, 10 and 25 h of culture, respectively, podophyllic acid concentration reached 99.9 +/- 12.3 mg/l, enhanced by 284% comparing to one-time addition (i.e. 26.0 +/- 2.1 mg/l). The fundamental information obtained in this study provides a simple and efficient way to produce podophyllic acid. (C) 2008 Elsevier Ltd. All rights reserved.

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