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Received March 13, 2009
Accepted March 16, 2009
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Production of bacterial cellulose in static conditions by a simple fed-batch cultivation strategy
Department of Chemical Engineering, Kyungpook National University, Daegu 702-701, Korea 1Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad, Pakistan
parkjk@knu.ac.kr
Korean Journal of Chemical Engineering, November 2009, 26(6), 1689-1692(4), 10.1007/s11814-009-0232-5
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Abstract
The current study investigated fed-batch cultivation for the increased productivity of bacterial cellulose (BC) sheets by Gluconacetobacter hansenii PJK in static conditions using chemically defined medium and waste from beer fermentation broth. Fermentations were carried out in a 3 L jar fermenter without any impeller for 30 days. In the proposed fed-batch cultivation, 500 mL of the medium was initially inoculated with pre-culture in a jar fermenter while a fresh medium was fed periodically. BC production was also done by using batch cultivation which was used as a control for comparison. The results obtained revealed an overall of 2-3 times increase in BC production in fedbatch cultivation compared to batch cultivation after 30 days of cultivation. During these experiments, it was found that waste from beer fermentation broth is a superior medium for the BC production using fed-batch cultivation. The production of water soluble oligosaccharides as useful by-products was also monitored during these investigations. Fed-batch cultivation and waste from beer fermentation was also found superior for the production of these by-products._x000D_
According to literature search and to the best of our knowledge, it is the first report of using fed-batch cultivation for BC production in static conditions.
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References
Khan T, Park JK, Kwon JH, Korean J. Chem. Eng., 24(5), 816 (2007)
Ishihara M, Matsunaga M, Hayashi N, Tisler V, Enzyme Microb. Technol., 31(7), 986 (2002)
Klemm D, Schumann D, Udhardt U, Marsch S, Prog. Polym. Sci., 26, 1561 (2001)
Vandamme EJ, Baets SD, Vanbaelen A, Joris K, Wulf PD, Polym. Degrad. Stab., 59, 93 (1998)
Serafica G, Mormino R, Bungay H, Appl. Microbiol. Biotechnol., 58(6), 756 (2002)
Dubey V, Saxena C, Singh L, Ramana KV, Chauhan RS, Sep. Purif. Technol., 27(2), 163 (2002)
Park JK, Park YH, Jung JY, Biotechnol. Bioprocess Eng., 8, 83 (2003)
Park JK, Jung JY, Park YH, Biotechnol. Lett., 25(24), 2055 (2003)
Park JK, Hyun SH, Jung JY, Biotechnol. Bioprocess Eng., 9, 383 (2004)
Jung JY, Park JK, Chang HN, Enzyme Microb. Technol., 37(3), 347 (2005)
Jung JY, Khan T, Park JK, Chang HN, Korean J. Chem. Eng., 24(2), 265 (2007)
Park JK, Hyun SH, Ahn WS, Korean Chem. Eng. Res., 44(1), 52 (2006)
Ha JH, Shehzad O, Khan S, Lee SY, Park JW, Khan T, Park JK, Korean J. Chem. Eng., 25(4), 812 (2008)
Khan T, Khan S, Park JK, Biotechnol. Bioprocess Eng., 13, 240 (2008)
Shoda M, Sugano Y, Biotechnol. Bioprocess Eng., 10, 1 (2005)
Khan T, Hyun SH, Park JK, Enzyme Microb. Technol., 42(1), 89 (2007)
Khan T, Park JK, Carbohydr. Polym., 73, 438 (2008)
Khan T, Khan H, Park JK, Process Biochem., 42, 252 (2007)
Ishihara M, Matsunaga M, Hayashi N, Tisler V, Enzyme Microb. Technol., 31(7), 986 (2002)
Klemm D, Schumann D, Udhardt U, Marsch S, Prog. Polym. Sci., 26, 1561 (2001)
Vandamme EJ, Baets SD, Vanbaelen A, Joris K, Wulf PD, Polym. Degrad. Stab., 59, 93 (1998)
Serafica G, Mormino R, Bungay H, Appl. Microbiol. Biotechnol., 58(6), 756 (2002)
Dubey V, Saxena C, Singh L, Ramana KV, Chauhan RS, Sep. Purif. Technol., 27(2), 163 (2002)
Park JK, Park YH, Jung JY, Biotechnol. Bioprocess Eng., 8, 83 (2003)
Park JK, Jung JY, Park YH, Biotechnol. Lett., 25(24), 2055 (2003)
Park JK, Hyun SH, Jung JY, Biotechnol. Bioprocess Eng., 9, 383 (2004)
Jung JY, Park JK, Chang HN, Enzyme Microb. Technol., 37(3), 347 (2005)
Jung JY, Khan T, Park JK, Chang HN, Korean J. Chem. Eng., 24(2), 265 (2007)
Park JK, Hyun SH, Ahn WS, Korean Chem. Eng. Res., 44(1), 52 (2006)
Ha JH, Shehzad O, Khan S, Lee SY, Park JW, Khan T, Park JK, Korean J. Chem. Eng., 25(4), 812 (2008)
Khan T, Khan S, Park JK, Biotechnol. Bioprocess Eng., 13, 240 (2008)
Shoda M, Sugano Y, Biotechnol. Bioprocess Eng., 10, 1 (2005)
Khan T, Hyun SH, Park JK, Enzyme Microb. Technol., 42(1), 89 (2007)
Khan T, Park JK, Carbohydr. Polym., 73, 438 (2008)
Khan T, Khan H, Park JK, Process Biochem., 42, 252 (2007)