Engineering Escherichia coli FAD synthetase for the biosynthesis of FAD nucleotide analogues results in aminoglycoside antibiotic tolerance

The presence of the adenosine moiety in flavin adenine dinucleotide (FAD), nicotimanide adenine dinculeotide, coenzyme A, and S-adenosylmethionine cofactors is intriguing as it appears to play no direct catalytic role. In FAD biosynthesis, the bifunctional FAD synthetase catalyzes FMN adenylation using ATP via its FMN adenylyltransferase (FMNAT) domain. Substituting ATP with alternative nucleotides in this reaction would enable the synthesis of FAD nucleotide analogues. This study explores nucleotide selectivity of theEscherichia coliFMNAT domain. Mutant enzyme variants were engineered which produce FAD analogues. Chromosomal substitution of the wild-typeE. coliFAD synthetase with a mutated version resulted in the intracellular synthesis of FAD analogues and conferred increased tolerance to aminoglycoside antibiotics. These findings validate the FMNAT domain loop as a viable site for cofactor engineering, with potential synthetic biology applications. Finally, the observed correlation between FAD analogue production and antibiotic tolerance reveals that there exist novel metabolic mechanisms underlying bacterial resistance.