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Microbiology 148 (2002), 1003-1013
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Microbiology (2002), 148, 1003-1013.
© 2002 Society for General Microbiology


Research Paper

Metabolic engineering of lactic acid bacteria, the combined approach: kinetic modelling, metabolic control and experimental analysis

Marcel H. N. Hoefnagel1,2, Marjo J. C. Starrenburg1,3, Dirk E. Martens1,2, Jeroen Hugenholtz1,3, Michiel Kleerebezem1,3, Iris I. Van Swam1,3, Roger Bongers1,3, Hans V. Westerhoff4 and Jacky L. Snoep4,5

Wageningen Centre for Food Sciences1 and Food and Bioprocess Engineering Group,2 Wageningen University, PO Box 8129, 6700 EV Wageningen, The Netherlands
NIZO Food Research, PO Box 20, 6710 BA, Ede, The Netherlands3
BioCentrum Amsterdam, Dept of Molecular Cell Physiology, Free University, De Boelelaan 1087, NL-1081 HV Amsterdam, The Netherlands4
Dept of Biochemistry, University of Stellenbosch, Private bag X1, Matieland 7602, Stellenbosch, South Africa5

Author for correspondence: Marcel H. N. Hoefnagel. Tel: +31 317 483435. Fax: +31 317 482237. e-mail: marcel.hoefnagel{at}algemeen.pk.wau.nl

Everyone who has ever tried to radically change metabolic fluxes knows that it is often harder to determine which enzymes have to be modified than it is to actually implement these changes. In the more traditional genetic engineering approaches ’bottle-necks’ are pinpointed using qualitative, intuitive approaches, but the alleviation of suspected ’rate-limiting’ steps has not often been successful. Here the authors demonstrate that a model of pyruvate distribution in Lactococcus lactis based on enzyme kinetics in combination with metabolic control analysis clearly indicates the key control points in the flux to acetoin and diacetyl, important flavour compounds. The model presented here (available at http://jjj.biochem.sun.ac.za/wcfs.html) showed that the enzymes with the greatest effect on this flux resided outside the acetolactate synthase branch itself. Experiments confirmed the predictions of the model, i.e. knocking out lactate dehydrogenase and overexpressing NADH oxidase increased the flux through the acetolactate synthase branch from 0 to 75% of measured product formation rates.

Keywords: Metabolic control analysis, in silico modelling, Lactococcus lactis, pyruvate distribution

Abbreviations: ALS, acetolactate synthase; LDH, L-lactate dehydrogenase; MCA, metabolic control analysis; NOX, NADH oxidase; (abbreviations used in rate reactions and equations are defined in Table 1)

The GenBank accession number for the sequence reported in this paper is AY046926.




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