Abstract
Queuosine (Q) is a modification of the wobble base in tRNAs that decode
NAC codons. It is ubiquitous in bacteria, including many pathogens.
Streptococcus mutans is an early colonizer of dental plaque
biofilm and a key player in dental caries. Using a combination of
genetic and physiological approaches, the predicted Q synthesis and
salvage pathways were validated in this organism. These experiments
confirmed that S. mutans can synthesize Q de novo through
similar pathways found in Bacillus subtilis and Escherichia
coli. However, S. mutans has a distinct salvage pathway compared
to these model organisms, as it uses a transporter belonging to the
Energy Coupling Factor (ECF) family controlled by a preQ
1-dependent riboswitch. Furthermore, Q levels in this
oral pathogen depended heavily on the media composition, suggesting that
micronutrients can affect Q-mediated translation efficiency.