ATP regeneration by ATPases for in vitro biotransformation

Biotechnol Adv. 2024 Jul-Aug:73:108377. doi: 10.1016/j.biotechadv.2024.108377. Epub 2024 May 17.

Abstract

Adenosine triphosphate (ATP) regeneration is a significant step in both living cells and in vitro biotransformation (ivBT). Rotary motor ATP synthases (ATPases), which regenerate ATP in living cells, have been widely assembled in biomimetic structures for in vitro ATP synthesis. In this review, we present a comprehensive overview of ATPases, including the working principle, orientation and distribution density properties of ATPases, as well as the assembly strategies and applications of ATPase-based ATP regeneration modules. The original sources of ATPases for in vitro ATP regeneration include chromatophores, chloroplasts, mitochondria, and inverted Escherichia coli (E. coli) vesicles, which are readily accessible but unstable. Although significant advances have been made in the assembly methods for ATPase-artificial membranes in recent decades, it remains challenging to replicate the high density and orientation of ATPases observed in vivo using in vitro assembly methods. The use of bioproton pumps or chemicals for constructing proton motive forces (PMF) enables the versatility and potential of ATPase-based ATP regeneration modules. Additionally, overall robustness can be achieved via membrane component selection, such as polymers offering great mechanical stability, or by constructing a solid supporting matrix through layer-by-layer assembly techniques. Finally, the prospects of ATPase-based ATP regeneration modules can be expected with the technological development of ATPases and artificial membranes.

Keywords: ATP regeneration; ATPase; Artificial membrane; Biotransformation; Proton motive force.

Publication types

  • Review

MeSH terms

  • Adenosine Triphosphatases* / metabolism
  • Adenosine Triphosphate* / metabolism
  • Biotransformation*
  • Escherichia coli / genetics
  • Escherichia coli / metabolism

Substances

  • Adenosine Triphosphate
  • Adenosine Triphosphatases