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Two-Step Fed-Batch Culture of Recombinant Escherichia coli for Production of Bacillus licheniformis Maltogenic Amylase  

Kim, Myoung-Dong (Department of Food Science and Technology and Research Center for New Bio-Materials in Agriculture, Seoul National University)
Lee, Woo-Jong (Department of Food Science and Technology and Research Center for New Bio-Materials in Agriculture, Seoul National University)
Park, Kwan-Hwa (Department of Food Science and Technology and Research Center for New Bio-Materials in Agriculture, Seoul National University)
Rhee, Ki-Hyeong (Department of Biological Science, Kongju National University)
Seo, Jin-Ho (Department of Food Science and Technology and Research Center for New Bio-Materials in Agriculture, Seoul National University)
Publication Information
Journal of Microbiology and Biotechnology / v.12, no.2, 2002 , pp. 273-278 More about this Journal
Abstract
Two-step fed-batch fermentations were carried out to overproduce Bacillus licheniformis maltogenic amylase (BLMA) in recombinant Escherichia coli. The first step was to increase the cell mass by controlling the feeding of a glucose solution, while the second step was designed to improve the amylase expression efficiency by supplementing organic nitrogen sources. The linear gradient feeding method was successfully adopted to maintain the glucose concentration below 0.2 g/l during the fed-batch mode, as effectively minimizing acetic acid formation. When the dissolved oxygen (DO) level became limiting, an accumulation of acetic acid and drastic decrease in specific BLMA productivity were observed. Glucose and organic nitrogen sources consisting of yeast extract and casein hydrolysate were simultaneously supplied in the pH-stat mode to further increase the specific BLMA expression efficiency. An organic nitrogen source consisting of 200 g/1 yeast extract and 100 g/1 casein hydrolysate was found to be the best among the various combinations tested. The feeding of an organic nitrogen source in the second-step fed-batch period was highly beneficial in enhancing the BLMA production. The optimized two-step fed-batch culture resulted in 78 g/l maximum dry cell mass and 443 U/ml maximum BLMA activity, corresponding to 1.5-fold increase in the dry cell mass and 3.7-fold enhancement in BLMA production, compared with the simple fed-batch fermentation.
Keywords
Bacillus licheniformis maltogenic amylase; recombinant E. coli; acetic acid; fed-batch; gradient feeding; organic nitrogen;
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1 Han, K., J. Hong, and H. C. Lim. 1993. Relieving effects of glycine and methionine from acetic acid and inhibition of Escherichia coli fermentation. Biotechnol. Bioeng. 41: 316- 324
2 Harrison, J. S., E. Keshavarz-Moore, P. Dunnill, M. J. Berry, A. Fellinger, and L. Frenken. 1997. Factors affecting the fermentative production of a lysozyme-binding antibody fragment in Escherichia coli. Biotechnol. Bioeng. 53: 611-622
3 Jung, G., P. Denefle, J. Becquart, and J. F. Mayaux. 1988. High-cell density fermentation studies of recombinant Escherichia coli strains expressing human interleukin-1. Ann. Inst. Pasteur Microbiol. 139: 12-14   DOI
4 Kim, C. I., M. D. Kim, Y. C. Park, N. S. Han, and J. H. Seo. 2000. Refolding of Bacillus macerans cyclodextrin glucanotransferase expressed as inclusion bodies in recombinant Escherichia coli. J. Microbiol. Biotechnol. 10: 632-637
5 Laemmli, U. K. 1970. Cleavage of structural proteins during assembly of the head of bacteriophage T4. Nature 27: 680- 685
6 Park, T. H., J. H. Seo, and H. C. Lim. 1989. Analysis of kinetic parameters for the 3b-indoleacrylic acid effect on trp promoter in Escherichia coli. Biotechnol. Lett. 11: 87-92
7 Yoon, S. K., W. K. Kang, and T. H. Park. 1994. Fed-batch operation of recombinant Escherichia coli containing trp promoter with controlled specific growth rate. Biotechnol. Bioeng. 43: 995-999
8 Lee, J. H., J. H. Kim, S. S. Hong, H. S. Lee, and C. S. Kim. 1999. Multimeric expression of antimicrobial peptide buforin II in Escherichia coli by fusion to a cystein-rich acidic peptide. J. Microbiol. Biotechnol. 9: 303-310
9 Nancib, N., C. Branlant, and J. Boudrant. 1991. Metabolic roles of peptone and yeast extract for the culture of a recombinant strain of Escherichia coli. J. Ind. Microbiol. 8: 165-170
10 Hellmuth, K., D. J. Korz, E. A. Sanders, and W. D. Deckwer. 1994. Effect of growth rate on stability and gene expression of recombinant plasmid during continuous high cell density cultivation of Escherichia coli TG1. J. Biotechnol. 32: 289- 298
11 Lee, S. Y. 1996. High cell density culture of Escherichia coli. Trends Biotech. 14: 98-105   DOI   ScienceOn
12 Weikert, C., U. Sauer, and J. E. Bailey. 1998. An Escherichia coli host strain useful for efficient overproduction of secreted recombinant protein. Biotechnol. Bioeng. 59: 386-391
13 Kim, G. J., I. Y. Lee, D. K. Choi, S. C. Yoon, and Y. H. Park. 1996. High cell density cultivation of Pseudomonas putida BM01 using glucose. J. Microbiol. Biotechnol. 6: 221-224
14 Chaplin, M. F. and J. F. Kennedy. 1986. Carbohydrate Analysis. Oxford: IRL Press. p. 2
15 Tomson, K., T. Paalme, P. S. Laakso, and R. Vilu. 1995. Automatic laboratory-scale fed-batch procedure for production of recombinant proteins using inducible expression systems of Escherichia coli. Biotechnol. Tech. 9: 793-798
16 Tsai, L. B., M. Mann, F. Morris, C. Rotgers, and D. Fenton. 1987. The effect of organic nitrogen and glucose on the production of recombinant human insulin-like growth factor in high cell density Escherichia coli fermentation. J. Ind. Microbiol. 2: 181-187
17 Nakano, K., M. Rischke, S. Sato, and H. Märkl. 1997. Influence of acetic acid on the growth of Escherichia coli K12 during high-cell density cultivation in a dialysis reactor. Appl. Microbiol. Biotechnol. 48: 597-601
18 Kim, I. C., J. H. Cha, J. R. Kim, S. Y. Jang, B. C. Seo, T. K. Cheong, D. S. Lee, Y. D. Choi, and K. H. Park. 1992. Catalytic properties of the cloned amylase from Bacillus licheniformis. J. Biol. Chem. 267: 22108-22114
19 Phue, J. N., S. J. Oh, Y. J. Son, Y. I. Kim, K. H. Kim, J. W. Kim, C. I. Hong, I. S. Chung, and T. R. Hahn. 2000. Improved refolding of recombinant human proinsulin from Escherichia coli in a two-stage reactor. J. Microbiol. Biotechnol. 10: 75-80
20 Weikert, C., U. Sauer, and J. E. Bailey. 1997. Use of a glycerol-limited, long-term chemostat for isolation of Escherichia coli mutants with improved physiological properties. Microbiol. 143: 1567-1574
21 Mignone, C. F. and C. Avignone Rossa. 1987. A simple method for designing fed-batch cultures with linear gradient feed of nutrients. Process Biochem. 28: 405-410
22 Han, K., H. C. Lim, and J. Hong. 1992. Acetic acid formation in Escherichia coli fermentation. Biotechnol. Bioeng. 39: 663-671
23 Wong, H. H., Y. C. Kim, S. Y. Lee, and H. N. Chang. 1998. Effect of post-induction nutrient feeding strategies on the production of bioadhesive protein in Escherichia coli. Biotechnol. Bioeng. 60: 271-276
24 Kim, B. S., S. C. Lee, S. Y. Lee, H. N. Chang, Y. K. Chang, and S. I. Woo. 1994. Production of poly (b-hydroxybutyric acid-co-b-hydroxyvaleric acid) by fed-batch culture of Alcaligenes eutrophus with glucose concentration control. Biotechnol. Bioeng. 43: 892-898
25 Riesenberg, D. and R. Guthke. 1999. High cell density cultivation of microorganisms. Appl. Micriobiol. Biotechnol. 51: 421-430
26 Koo, T. Y. and T. H. Park. 1999. Increased production of recombinant proteins by Escherichia coli deficient in acetic acid formation. J. Microbiol. Biotechnol. 9: 789-793
27 Riesenberg, D., V. Schulz, W. A. Knorre, H. D. Pohl, D. Korz, E. A. Sanders, A. Rob, and W. D. Decker. 1991. High cell density cultivation of Escherichia coli at controlled specific growth rate. J. Biotechnol. 20: 17-28
28 Shin, C. S., M. S. Hong, C. S. Bae, and J. Lee. 1997. Enhanced production of human mini-proinsulin in fed-batch cultures at high cell density of Escherichia coli BL21 (DE3)[pET-3aT2M2]. Biotechnol. Prog. 13: 249-257.
29 Kim, H. Y., C. W. Kim, and Y. J. Choi. 2000. Cloning and expression of inulin fructotransferase gene of Arthrobacter sp. A-6 in Escherichia coli and Bacillus subtilis. J. Microbiol. Biotechnol. 10: 275-280
30 Lee, C. W., M. B. Gu, and H. N. Chang. 1989. High-density culture of Escherichia coli carrying recombinant plasmid in a membrane cell recycle fermenter. Enz. Microb. Technol. 11: 49-54