Multiphase Bioreactor Design

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biocatalyst can be avoided by making the pores sufficiently small, i.e. smaller than the
critical cluster size.
Selection of the mode of operation for a specific solid-to-solid bioconversion, batch at
high concentrations of undissolved substrate or continuous, is often based on the costs
(per kg of product produced). By assuming that in both batch and continuous solid-to-
solid bioconversions the bioconversion is rate limiting, and by introducing a number of
simplifications, the costs of batch operation were compared with the costs of continuous
operation. This revealed that a batch system can only compete with a continuous system
if both the conversion is 100% and the productivity of the biocatalyst is maximal.


ACKNOWLEDGEMENTS

This work was financially supported by the Ministry of Economic Affairs, the Ministry of
Education, Culture and Science, the Ministry of Agriculture, Nature Management and
Fishery in the framework of an industrially relevant research programme of the
Netherlands Association of Biotechnology Centres in the Netherlands (ABON).


REFERENCES

Adelhorst, K., Björkling, F., Godtfredsen, S.E., Kirk, O. (1990) Enzyme catalysed preparation of
6– 0 -acyl-glucopyranosides. Synthesis 2, 112–115.
Andersson, E., Hahn-Hägerdal, B. (1990) Bioconversions in aqueous two-phase systems. Enzyme
Microb Technol 12, 242–253.
Bennett, R.C. (1993) Crystallizer selection and design. In: Myerson A.S., editor. Handbook of
industrial crystallization. Boston: Butterworth-Heinemann. p. 103–130.
Bornscheuer, U.T., Yamane, Y. (1994) Activity and stability of lipase in the solid phase
glycerolysis of triolein. Enzyme Microb Technol 16, 864–869.
Cao, L., Bornscheuer, U.T., Schmid, R.D. (1996) Lipase-catalysed solid phase synthesis of sugar
esters. Fett/Lipid 98, 332–335.
Čeřovský, V. (1992) Protease-catalysed peptide synthesis in solvent-free system. Biotechnol Tech
6, 155–160.
Eichhorn, U., Bommarius, A.S., Drauz, K., Jakubke, H-D. (1995) Environmentally acceptable
synthesis of peptides in high yields by suspension-to-suspension conversion via protease
catalysis. In: Maia HLS, editor. Peptides 1994. Leiden, The Netherlands: ESCOM. p. 226–227.
Eichhorn, U., Bommarius, A.S., Drauz, K., Jakubke, H-D. (1997) Synthesis of dipeptides by
suspension-to-suspension conversion via thermolysin catalysis: from analytical to preparative
scale. J Pep Sci 3, 254–251.
Erbeldinger, M., Xiongwei, N., Hailing, P.J. (1998a) Effect of water and enzyme concentration on
thermolysin-catalysed solid-to-solid peptide synthesis. Biotechnol Bioeng 59, 68–72.
Erbeldinger, M., Xiongwei, N., Hailing, P.J. (1998b) Enzymatic synthesis with mainly undissolved
substrates at very high concentrations. Enzyme Microb Technol 23, 141–148.
Fregapane, G., Sarney, D.B., Vulfson, E.N. (1991) Enzymic solvent-free synthesis of sugar acetal
fatty acid esters. Enzyme Microb Technol 13, 796–800.
Gill, I., Vulfson, E.N. (1993) Enzymatic synthesis of short peptides in heterogeneous mixtures of
substrates. J Am Chem Soc 115, 3348–3349.
Gill, I., Vulfson, E.N. (1994) Enzymatic catalysis in heterogeneous eutectic mixtures of substrates.
Trends Biotechnol 12, 118–122.


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