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In vivo kinetic analysis of the penicillin biosynthesis pathway using PAA stimulus response experiments.

Authors :
Deshmukh AT
Verheijen PJT
Maleki Seifar R
Heijnen JJ
van Gulik WM
Source :
Metabolic engineering [Metab Eng] 2015 Nov; Vol. 32, pp. 155-173. Date of Electronic Publication: 2015 Oct 19.
Publication Year :
2015

Abstract

In this study we combined experimentation with mathematical modeling to unravel the in vivo kinetic properties of the enzymes and transporters of the penicillin biosynthesis pathway in a high yielding Penicillium chrysogenum strain. The experiment consisted of a step response experiment with the side chain precursor phenyl acetic acid (PAA) in a glucose-limited chemostat. The metabolite data showed that in the absence of PAA all penicillin pathway enzymes were expressed, leading to the production of a significant amount of 6-aminopenicillanic acid (6APA) as end product. After the stepwise perturbation with PAA, the pathway produced PenG within seconds. From the extra- and intracellular metabolite measurements, hypotheses for the secretion mechanisms of penicillin pathway metabolites were derived. A dynamic model of the penicillin biosynthesis pathway was then constructed that included the formation and transport over the cytoplasmic membrane of pathway intermediates, PAA and the product penicillin-G (PenG). The model parameters and changes in the enzyme levels of the penicillin biosynthesis pathway under in vivo conditions were simultaneously estimated using experimental data obtained at three different timescales (seconds, minutes, hours). The model was applied to determine changes in the penicillin pathway enzymes in time, calculate fluxes and analyze the flux control of the pathway. This led to a reassessment of the in vivo behavior of the pathway enzymes and in particular Acyl-CoA:Isopenicillin N Acyltransferase (AT).<br /> (Copyright © 2015 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1096-7184
Volume :
32
Database :
MEDLINE
Journal :
Metabolic engineering
Publication Type :
Academic Journal
Accession number :
26476338
Full Text :
https://doi.org/10.1016/j.ymben.2015.09.018