Unstructured kinetic models to simulate an arabinose switch that decouples cell growth from metabolite production

dc.contributor.authorEdwards, Harley
dc.contributor.authorXu, Peng
dc.date.accessioned2020-08-06T16:38:59Z
dc.date.available2020-08-06T16:38:59Z
dc.date.issued2020-07-14
dc.description.abstractModeling synthetic gene circuits to implement dynamic flux balancing is crucial in teaching and exploring metabolic engineering strategies to repartition metabolic precursors and construct efficient microbial cell factories. Microbial fitness and production rates are often complex phenotypes that are governed by highly non-linear, multivariable functions which are intrinsically linked through carbon metabolism. The solution of such dynamic system can be difficult for synthetic biologists to visualize or conceptualize. Recently, researchers (Santala et al., Metab. Eng. Comm., 2018) have implemented an arabinose based genetic switch to dynamically partition the central carbon flux between cell growth and product formation. The autonomous switch allowed dynamic shift from arabinose-associated cell growth to acetate-associated product (wax ester) formation. This system clearly demonstrates the effectiveness of using a genetic switch to decouple cell growth from product formation in a one-pot bioreactor to minimize operational cost. Coupled with Michaelis-Menten kinetics, and Luedeking-Piret equations, we were able to reconstruct and analyze this metabolic switch in silica and achieved graphical solutions that qualitatively match with the experimental data. By assessing physiologically-accessible parameter space, we observed a wide range of dynamic behavior and examined the different limiting cases. Graphical solutions for this dynamic system can be viewed simultaneously and resolved in real time via buttons on the graphical user interface (GUI). Metabolic bottlenecks in the system can be accurately predicted by varying the respective rate constants. The GUI serves as a diagnosis toolkit to troubleshoot genetic circuits design constraints and as an interactive workflow of using this arabinose based genetic switch to dynamically control carbon flux, which may provide a valuable computational toolbox for metabolic engineers and synthetic biologists to simulate and understand complex genetic-metabolic system.en_US
dc.description.sponsorshipThe authors would like to acknowledge the Bill and Melinda Gates Foundation (OPP1188443) and National Science Foundation under grant number 1805139 for financially supporting this project. The authors would also like to acknowledge the discussion of this project with the ENCH482/682 and ENCH640 students at the University of Maryland Baltimore County in the Fall 2018 and Spring 2019.en_US
dc.description.urihttps://www.sciencedirect.com/science/article/pii/S2405805X2030048Xen_US
dc.format.extent8 pagesen_US
dc.genrejournal articlesen_US
dc.identifierdoi:10.13016/m2pmtn-i4mf
dc.identifier.citationEdwards, Harley; Xu, Peng; Unstructured kinetic models to simulate an arabinose switch that decouples cell growth from metabolite production; Synthetic and Systems Biotechnology Volume 5, Issue 3 (2020) Pages 222-229; https://www.sciencedirect.com/science/article/pii/S2405805X2030048Xen_US
dc.identifier.urihttps://doi.org/10.1016/j.synbio.2020.07.003
dc.identifier.urihttp://hdl.handle.net/11603/19355
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Chemical, Biochemical & Environmental Engineering Department Collection
dc.relation.ispartofUMBC Student Collection
dc.relation.ispartofUMBC Faculty Collection
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.titleUnstructured kinetic models to simulate an arabinose switch that decouples cell growth from metabolite productionen_US
dc.typeTexten_US

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