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Received September 30, 2015
Accepted December 19, 2015
- 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 polyhydroxyalkanoates by batch and fed-batch cultivations of Bacillus megaterium from acid-treated red algae
Department of Chemical Engineering, Chungbuk National University, Cheongju, Chungbuk 28644, Korea
bskim@chungbuk.ac.kr
Korean Journal of Chemical Engineering, May 2016, 33(5), 1669-1673(5), 10.1007/s11814-015-0293-6
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Abstract
Polyhydroxyalkanoates (PHAs) are linear polyesters synthesized by microbial fermentation of various substrates. PHAs are accumulated in microbial cells in order to store carbon and energy for future use. We used acid-pretreated red alga (Gelidium amansii) as a cheap, abundant carbon source to produce PHA via batch and fed-batch cultivation of Bacillus megaterium KCTC 2194. After acid treatment of 10% (w/v) G. amansii, 25.5 g/L galactose, 3.6 g/L glucose, 6 g/L 5-HMF, and 1.05 g/L levulinic acid were formed. In batch culture at pH 7, the dry cell weight (DCW) and PHA content increased to 5.5 g/L and 51.4%, respectively. The cell concentration was enhanced by fed-batch cultivation using two feeding strategies: pH-stat and intermittent feeding. When the pH-stat feeding strategy was employed to add concentrated hydrolysate to the fermentor, DCW increased to 8.2 g/L, with 53.2% PHA content. When concentrated hydrolysate was fed using the intermittent feeding strategy, higher DCW (10.1 g/L) was obtained, along with a slight increase of PHA content to 54.5%. This study demonstrates that red algae could be used after simple acid treatment, to produce PHA without steps for enzymatic hydrolysis and inhibitor removal.
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References
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Valappil SP, Misra SK, Boccaccini AR, Keshavarz T, Bucke C, Roy I, J. Biotechnol., 132, 251 (2007)
Reddy SV, Thirumala M, Mahmood S, World J. Microbiol. Biotechnol., 25, 391 (2009)
Jeffcoat R, Biochem. Soc. Trans., 17, 1137 (1989)
Alkotaini B, Sathiyamoorthi E, Kim BS, Biotechnol. Bioproc. Eng., 20, 856 (2015)
Palmqvist E, Hahn-Hagerdal B, Bioresour. Technol., 74(1), 25 (2000)
Labuzek S, Radecka I, J. Appl. Microbiol., 90(3), 353 (2001)
Gao X, Yuan XX, Shi ZY, Guo YY, Shen XW, Chen JC, Wu Q, Chen GQ, Microb. Cell Fact., 11, 130 (2012)
Lopez J, Naranjo J, Higuita J, Cubitto M, Cardona C, Villar M, Biotechnol. Bioproc. Eng., 17, 250 (2012)
Sun Z, Ramsay JA, Guay M, Ramsay B, J. Biotechnol., 132, 280 (2007)
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Pandian SR, Deepak V, Kalishwaralal K, Rameshkumar N, Jeyaraj M, Gurunathan S, Bioresour. Technol., 101(2), 705 (2010)
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