Abstract
A novel microfiltration batch culture process, suitable for scale-up, has been designed, instrumented, and studied with a representative recombinant-DNA receptor strain of Escherichia coli. In this process nutrient medium is fed continuously into an aerated and stirred fermentor, and metabolic products are withdrawn continuously at the same rate by crossflow microfiltration in an external recycle loop, so that product inhibition of cell growth is relieved. The maximum density of cells is increased fivefold more than in the control process, and is limited by acetic and other organic acids accumulating from the aerobic fermentation of excess glucose.
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References
Sortland, L.D. and Wilke, C.R. 1969. Growth of Streptococcus faecalus in dense culture. Biotechnol. Bioeng. 11: 805–841.
Schultz, J.S. and Gerhardt, P. 1969. Dialysis culture of microorganisms: design, theory, and results. Bacteriol. Rev. 33: 1–47.
Stieber, R.W. and Gerhardt, P. 1981. Dialysis continuous process for ammonium lactate fermentation: simulated and experimental dialy-sate-feed, immobilized-cell systems. Biotechnol. Bioeng. 23: 535–549.
Kyung, K.H. and Gerhardt, P. 1984. Continuous production of ethanol by yeast “immobilized” in a membrane-contained fermentor. Biotechnol. Bioeng. 26: 252–256.
Pirt, S.J. and Kurowski, W.M. 1970. An extension of the theory of the chemostat with feedback of organisms. Its experimental realization with a yeast culture. J. Gen. Microbiol. 63: 357–366.
Watson, D.C. and Berry, D.R. 1979. Use of an exchange nitration technique to obtain synchronous sporulation in an extended batch fermentation. Biotechnol. Bioeng. 21: 213–220.
Rogers, P.L., Lee, K.J., Skotnicki, M.L. and Tribe, D.E. 1982. Ethanol production by Zymomonas mobilis. Adv. Biochem. Eng. 23: 37–84.
Dostálek, M. and Häggstrom, M. 1982. A filter fermentor-apparatus and control equipment. Biotechnol. Bioeng. 24: 2077–2086.
Charley, R.C., Fein, J.E., Lavers, B.H., Lawford, H.G. and Lawford, G.R. 1983. Optimization of process design for continuous ethanol production by Zymomonas mobilis ATCC 29191. Biotechnol. Letters 5: 169–174.
Janssens, J.H., Bernard, A. and Bailey, R.B. 1984. Ethanol from whey: continuous fermentation with cell recycle. Biotech. Bioeng. 26: 1–5.
Gallup, D.M. and Gerhardt, P. 1963. Dialysis fermentor systems for concentrated culture of microorganisms. Appl. Microbiol. 2: 506–512.
Stieber, R.W. 1979. Dialysis continuous processes for microbial fermentations: mathematical models, computer simulations, and experimental tests. Michigan State University, E. Lansing, Mich. (Ph. D. thesis).
Tanny, G.B., Mirelman, D. and Pistole, F. 1980. Improved filtration technique for concentrating and harvesting bacteria. Appl. Environ. Microbiol. 40: 269–273.
Anderson, K.W., Grulke, E.A. and Gerhardt, P. 1984. Liquid level control in an aerated continuous flow fermenter. Paper presented at the 188th National Meeting of the American Chemical Society, Division of Microbial and Biochemical Technology, Phil. PA, 26–31 August, 1984.
Amarasingham, C.R. and Davis, B.D. 1965. Regulation of α-ketoglutarate dehydrogenase formation in Esherichia coli. J. Biol. Chem. 240: 3664–3668.
Doelle, H.W., Hollywood, N. and Westwood, A.W. 1974. Effect of glucose concentration on a number of enzymes involved in the aerobic and anaerobic utilization of glucose in turbidostat cultures of Escherichia coli. Microbios 9: 221–232.
Hollywood, N. and Doelle, H.W. 1976. Effect of specific growth rate and glucose concentration on growth and glucose metabolism of Escherichia coli K-12. Microbios 17: 23–33.
Doelle, H.W., Ewings, K.N. and Hollywood, N.W. 1982. Regulation of glucose metabolism in bacterial systems. Adv. Biochem. Eng. 23: 1–35.
Bolivar, F. and Backman, K. 1979. Plasmids of Escherichia coli as cloning vectors. Methods Enzymol. 68: 245–267.
Boyer, H.W. and Roulland-Dussoix, D. 1969. A complementation analysis of the restriction and modification of DNA in Escherichia coli. J. Mol. Biol. 41: 459–472.
Dubois, M., Gilles, K.A., Hamilton, J.K., Rebers, P.A. and Smith, F. 1956. Colorimetric method for determination of sugars and related substances. Anal. Chem. 28: 350–356.
Johnson, R.R., Balwani, T.L., Johnson, L.J., McClure, K.E. and Dehority, B.A. 1966. Corn plant maturity. II. Effects on in vitro cellulose digestability and soluble carbohvdrate content. J. Animal Sci. 25: 617–623.
Montgomery, R. 1961. Further studies of the phenol-sulfuric acid reagent for carbohydrates. Biochim. Biophys. Acta. 48: 591–593.
Johnson, M. 1941. Isolation and properties of a pure yeast polypeptidase. J. Biol. Chem. 137: 575–586.
Supelco, Inc. 1975. Extraction procedures for GC analysis of culture by-products for volatile acids and alcohols. Bulletin Supplement 748G.
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Anderson, K., Grulke, E. & Gerhardt, P. Microfiltration Culture Process for Enhanced Production of rDNA Receptor Cells of Escherichia Coli. Nat Biotechnol 2, 891–896 (1984). https://doi.org/10.1038/nbt1084-891
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DOI: https://doi.org/10.1038/nbt1084-891