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http://dx.doi.org/10.4014/jmb.1206.06057

Media Optimization of Corynebacterium glutamicum for Succinate Production Under Oxygen-Deprived Condition  

Jeon, Jong-Min (Department of Microbial Engineering, Konkuk University)
Thangamani, Rajesh (Department of Microbial Engineering, Konkuk University)
Song, Eunjung (School of Chemical and Biological Engineering, Seoul National University)
Lee, Hyuk-Won (Biotechnology Process Engineering Center)
Lee, Hong-Weon (Biotechnology Process Engineering Center)
Yang, Yung-Hun (Department of Microbial Engineering, Konkuk University)
Publication Information
Journal of Microbiology and Biotechnology / v.23, no.2, 2013 , pp. 211-217 More about this Journal
Abstract
Corynebacterium glutamicum is one of the well-studied industrial strain that is used for the production of nucleotides and amino acids. Recently, it has also been studied as a possible producer of organic acids such as succinic acid, based on its ability to produce organic acids under an oxygen deprivation condition. In this study, we conducted the optimization of medium components for improved succinate production from C. glutamicum under an oxygen deprivation condition by Plackett-Burman design and applied a response surface methodology. A Plackett-Burman design for ten factors such as glucose, ammonium sulfate, magnesium sulfate, potassium phosphate ($K_2HPO_4$ and $KH_2PO_4$), iron sulfate, manganese sulfate, biotin, thiamine, and sodium bicarbonate was applied to evaluate the effects on succinate production. Glucose, ammonium sulfate, magnesium sulfate, and dipotassium phosphate were found to have significant influence on succinate production, and the optimal concentrations of these four factors were sequentially investigated by the response surface methodology using a Box-Behnken design. The optimal medium components obtained for achieving maximum concentration of succinic acid were as follows: glucose 10 g/l, magnesium sulfate 0.5 g/l, dipotassium phosphate ($K_2HPO_4$) 0.75 g/l, potassium dihydrogen phosphate ($KH_2PO_4$) 0.5 g/l, iron sulfate 6 mg/l, manganese sulfate 4.2 mg/l, biotin 0.2 mg/l, thiamine 0.2 mg/l, and sodium bicarbonate 100 mM. The parameters that differed from a normal BT medium were glucose changed from 40 g/l to 10 g/l, dipotassium phosphate ($K_2HPO_4$) 0.5 g/l changed to 0.75 g/l, and ammonium sulfate ($(NH_4)_2SO_4$) 7 g/l changed to 0 g/l. Under these conditions, the final succinic acid concentration was 16.3 mM, which is about 1.46 fold higher than the original medium (11.1 mM) at 24 h. This work showed the improvement of succinate production by a simple change of media components deduced from sequential optimization.
Keywords
Succinic acid production; Plackett-Burman design; response surface methodology; fermentation;
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1 Chae, Y. K. and J. L. Markley. 2000. Functional recombinant rabbit muscle phosphoglucomutase from Escherichia coli. Protein Expr. Purif. 20: 124-127.   DOI   ScienceOn
2 Guettler, M. V. and M. Jain. 1996. Method for making succinic acid, Anaerobiospirillum succiniciproducens variants for use in process and methods for obtaining variants. US patent 5,521,075.
3 Corma, A., S. Iborra, and A. Velty. 2007. Chemical routes for the transformation of biomass into chemicals. Chem. Rev. 107: 2411-2502.   DOI   ScienceOn
4 Fink, D., N. Weissschuh, J. Reuther, W. Wohlleben, and A. Engels. 2002. Two transcriptional regulators GlnR and GlnRII are involved in regulation of nitrogen metabolism in Streptomyces coelicolor A3(2). Mol. Microbiol. 46: 331-347.   DOI   ScienceOn
5 Goodchild, J. A. and C. V. Givan. 1990. Influence of ammonium and extracellular pH on the amino and organic acid contents of suspension culture cells of Acer pseudoplatanus. Physiol. Plant 78: 29-37.   DOI
6 Guettler, M. V., D. Rumler, and M. K. Jain. 1999. Actinobacillus succinogenes sp. nov., a novel succinic-acid-producing strain from the bovine rumen. Int. J. Syst. Bacteriol. 49: 207-216.   DOI   ScienceOn
7 Hachiya, T., C. K. Watanabe, M. Fujimoto, T. Ishikawa, K. Takahara, M. Kawai-Yamada, et al. 2012. Nitrate addition alleviates ammonium toxicity without lessening ammonium accumulation, organic acid depletion and inorganic cation depletion in Arabidopsis thaliana shoots. Plant Cell Physiol. 53: 577-591.   DOI   ScienceOn
8 Inui, M., S. Murakami, S. Okino, H. Kawaguchi, A. A. Vertes, and H. Yukawa. 2004. Metabolic analysis of Corynebacterium glutamicum during lactate and succinate productions under oxygen deprivation conditions. J. Mol. Microbiol. Biotechnol. 7: 182-196.   DOI   ScienceOn
9 Inui, M., M. Suda, S. Kimura, K. Yasuda, H. Suzuki, H. Toda, et al. 2008. Expression of Clostridium acetobutylicum butanol synthetic genes in Escherichia coli. Appl. Microbiol. Biotechnol. 77: 1305-1316.   DOI   ScienceOn
10 Lee, K., H. S. Joo, Y. H. Yang, E. Song, and B. G. Kim. 2006. Proteomics for Streptomyces: "Industrial proteomics" for antibiotics. J. Microbiol. Biotechnol. 16: 331-348.
11 Jantama, K., X. Zhang, J. C. Moore, K. T. Shanmugam, S. A. Svoronos, and L. O. Ingram. 2008. Eliminating side products and increasing succinate yields in engineered strains of Escherichia coli C. Biotechnol. Bioeng. 101: 881-893.   DOI   ScienceOn
12 Krause, J. P., T. Polen, J. W. Youn, D. Emer, B. J. Eikmanns, and V. F. Wendisch. 2012. Regulation of the malic enzyme gene malE by the transcriptional regulator MalR in Corynebacterium glutamicum. J. Biotechnol. 159: 204-215.   DOI   ScienceOn
13 Kurzrock, T. and D. Weuster-Botz. 2010. Recovery of succinic acid from fermentation broth. Biotechnol. Lett. 32: 331-339.   DOI
14 Lee, P. C., S. Y. Lee, S. H. Hong, and H. N. Chang. 2002. Isolation and characterization of a new succinic acid-producing bacterium, Mannheimia succiniciproducens MBEL55E, from bovine rumen. Appl. Microbiol. Biotechnol. 58: 663-668.   DOI   ScienceOn
15 Yu, P., Y. A. Yan, and Y. P. Tang. 2011. Medium optimization for endochitinase production by recombinant Pichia pastoris ZJGSU02 using response surface methodology. Afr. J. Biotechnol. 10: 75-84.
16 Litsanov, B., M. Brocker, and M. Bott. 2012. Toward homosuccinate fermentation: Metabolic engineering of Corynebacterium glutamicum for anaerobic production of succinate from glucose and formate. Appl. Environ. Microbiol. 78: 3325-3337.   DOI
17 Ma, F. X., J. H. Kim, S. B. Kim, Y. G. Seo, Y. K. Chang, S. K. Hong, and C. J. Kim. 2008. Medium optimization for enhanced production of rifamycin B by Amycolatopsis mediterranei S699: Combining a full factorial design and a statistical approach. Process Biochem. 43: 954-960.   DOI   ScienceOn
18 Oh, I. J., D. H. Kim, E. K. Oh, S. Y. Lee, and J. Lee. 2009. Optimization and scale-up of succinic acid production by Mannheimia succiniciproducens LPK7. J. Microbiol. Biotechnol. 19: 167-171.   DOI
19 Okino, S., M. Inui, and H. Yukawa. 2005. Production of organic acids by Corynebacterium glutamicum under oxygen deprivation. Appl. Microbiol. Biotechnol. 68: 475-480.   DOI   ScienceOn
20 Okino, S., R. Noburyu, M. Suda, T. Jojima, M. Inui, and H. Yukawa. 2008. An efficient succinic acid production process in a metabolically engineered Corynebacterium glutamicum strain. Appl. Microbiol. Biotechnol. 81: 459-464.   DOI   ScienceOn
21 Song, H., Y. S. Huh, S. Y. Lee, W. H. Hong, and Y. K. Hong. 2007. Recovery of succinic acid produced by fermentation of a metabolically engineered Mannheimia succiniciproducens strain. J. Biotechnol. 132: 445-452.   DOI   ScienceOn