Chemiosmotic nutrient transport in synthetic cells powered by electrogenic antiport coupled to decarboxylation

Cellular homeostasis depends on the supply of metabolic energy in the form of ATP and electrochemical ion gradients. The construction of synthetic cells requires a constant supply of energy to drive membrane transport and metabolism. Here, we provide synthetic cells with long-lasting metabolic energy in the form of an electrochemical proton gradient. Leveraging the L-malate decarboxylation pathway we generate a stable proton gradient and electrical potential in lipid vesicles by electrogenic L-malate/L-lactate exchange coupled to L-malate decarboxylation. By co-reconstitution with the transporters GltP and LacY, the synthetic cells maintain accumulation of L-glutamate and lactose over periods of hours, mimicking nutrient feeding in living cells. We couple the accumulation of lactose to a metabolic network for the generation of intermediates of the glycolytic and pentose phosphate pathways. This study underscores the potential of harnessing a proton motive force via a simple metabolic network, paving the way for the development of more complex synthetic systems.

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Publication Details

Journal
Nature Communications
Published
2024-09-12
DOI
https://doi.org/10.1038/s41467-024-52085-z
Citations
3
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
0.80

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article

Chemiosmotic nutrient transport in synthetic cells powered by electrogenic antiport coupled to decarboxylation

Bert Poolman, Miyer Patiño-Ruiz, Bauke Gaastra, Zaid R. Anshari et al.
3 citations
Nature Communications
Photoreceptor and optogenetics research
0.80
article

Chemiosmotic nutrient transport in synthetic cells powered by electrogenic antiport coupled to decarboxylation

Bert Poolman, Miyer Patiño-Ruiz, Bauke Gaastra, Zaid R. Anshari, Dirk Jan Slotboom
article en
3 citations

Abstract

Cellular homeostasis depends on the supply of metabolic energy in the form of ATP and electrochemical ion gradients. The construction of synthetic cells requires a constant supply of energy to drive membrane transport and metabolism. Here, we provide synthetic cells with long-lasting metabolic energy in the form of an electrochemical proton gradient. Leveraging the L-malate decarboxylation pathway we generate a stable proton gradient and electrical potential in lipid vesicles by electrogenic L-malate/L-lactate exchange coupled to L-malate decarboxylation. By co-reconstitution with the transporters GltP and LacY, the synthetic cells maintain accumulation of L-glutamate and lactose over periods of hours, mimicking nutrient feeding in living cells. We couple the accumulation of lactose to a metabolic network for the generation of intermediates of the glycolytic and pentose phosphate pathways. This study underscores the potential of harnessing a proton motive force via a simple metabolic network, paving the way for the development of more complex synthetic systems.

Nature CommunicationsVol. 15(1)
University of Groningen (NL)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Affordable and clean energy
Openalex Percentile: Top 29%
Photoreceptor and optogenetics research
0.80
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Chemiosmotic nutrient transport in synthetic cells powered by electrogenic antiport coupled to decarboxylation — Bert Poolman, Miyer Patiño-Ruiz, et al. · Nature Communications (2024) | TGRS Research Map | TGRS