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

Miyer F Patiño-Ruiz, Zaid Ramdhan Anshari, Bauke Gaastra, Dirk J Slotboom, Bert Poolman*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

27 Downloads (Pure)

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.

Original languageEnglish
Article number7976
Number of pages19
JournalNature Communications
Volume15
Issue number1
DOIs
Publication statusPublished - 12-Sept-2024

Keywords

  • Decarboxylation
  • Malates/metabolism
  • Glutamic Acid/metabolism
  • Biological Transport
  • Artificial Cells/metabolism
  • Lactic Acid/metabolism
  • Lactose/metabolism
  • Escherichia coli/metabolism
  • Nutrients/metabolism
  • Proton-Motive Force
  • Antiporters/metabolism
  • Glycolysis
  • Metabolic Networks and Pathways
  • Protons
  • Pentose Phosphate Pathway

Fingerprint

Dive into the research topics of 'Chemiosmotic nutrient transport in synthetic cells powered by electrogenic antiport coupled to decarboxylation'. Together they form a unique fingerprint.

Cite this