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Combining evolution and machine learning-guided pathway optimization to engineer a novel methylsuccinate module for synthetic C1 metabolism in vivo

Helena Schulz-MirbachiD, Vittorio RainaldiiD, Nitin BohraiD, Katsutaka Suzuki, Titouan Danet, Huda Kasim, Ari SatanowskiiD, Hai HeiD, Elena Rossini, Seung Hwan Lee, Melanie Klose, Jörg KahntiD, Timo GlatteriD, Peter ClausiD, Nicole PacziaiD, Beau B. DronsellaiD, Shanshan LuoiD, Nico J. ClaassensiD, Tobias J. ErbiD

PDFDOI

Abstract

De novo metabolic pathways open possibilities for sustainable biotransformations in microbes. However, the in vivo-implementation of such new-to-nature pathways is highly challenging and heavily relies on adaptive laboratory evolution (ALE) of the hosts native metabolic network. Here, we assess how much this need for host-centric ALE can be overcome and/or complemented through the informed design of the newly introduced pathway. Exemplifying for a synthetic CO2-fixation module via methyl-succinate, we established methylsuccinate-dependent growth of Escherichia coli over six months by ALE of E. colis native metabolism. In parallel, we developed a machine-learning guided workflow (MEVIS) for the automated engineering of the synthetic pathway, resulting in methylsuccinate-dependent growth within three weeks. Critically, performing MEVIS in the background of the ALE-evolved strain is necessary to further approach wild-type like growth, demonstrating how ALE in combination with machine-learning-guided lab automation holds great potential to accelerate and improve design-build-test-learn cycles in contemporary metabolic engineering.

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