With the advantages of simple genetic composition, low
metabolic
background, low energy waste, and high genetic stability, genome-reduced
strains, as promising functional chassis, have become an intensive
direction for constructing potent biosynthesis factories. Herein,
an innovative Genome-Reduced strain-based Active Cell-free Easy-to-make-protein
(GRACE) system is built as minimal transcription–translation
machinery. In this study, two Escherichia coli genome-reduced strains, ΔW3110 and ΔMG1655, with genome
reduction of 11.53% and 37.85%, are fused with the cell-free transcription–translation
(CFTT) system. The GRACE systems perform better than the corresponding
CFTT systems derived from their parental strains in representative
valuable applications, such as the expression and solubilization of
membrane proteins or protein polymers, biosensing of inorganic or
organic molecules based on different principles, and unnatural amino
acid embedding. Obviously, the GRACE system has provided a brand-new
enabling platform for cell-free transcription–translation basic
and applied studies and also would inspire the potential of genome-reduced
strains for versatile applications.