Abstract5′-End maturation of tRNA primary transcripts is thought to be ubiquitously catalyzed by ribonuclease P (RNase P), a ribonucleoprotein enzyme in the vast majority of organisms and organelles. In the hyperthermophilic bacteriumAquifex aeolicus, neither a gene for the RNA nor the protein component of bacterial RNase P has been identified in its sequenced genome. Here, we demonstrate the presence of an RNase P-like activity in cell lysates ofA. aeolicus. Detection of activity was sensitive to the buffer conditions during cell lysis and partial purification, explaining why we failed to observe activity in the buffer system applied previously. RNase P-like activity ofA. aeolicusdepends on the presence of Mg2+or Mn2+, persists at high temperatures, which inactivate RNase P enzymes from mesophilic bacteria, and is remarkably resistant to micrococcal nuclease treatment. While cellular RNA fractions from otherAquificales(A. pyrophilus,Hydrogenobacter thermophilus andThermocrinis ruber) could be stimulated by bacterial RNase P proteins to catalyze tRNA 5′-end maturation, no such stimulation was observed with RNA fromA. aeolicus. In conclusion, our results point to the possibility that RNase P-like activity inA. aeolicusis devoid of an RNA subunit or may include an RNA subunit with untypical features.
Homologs of
aquifex aeolicus
protein‐only RNase P are not the major RNase P activities in the archaea
haloferax volcanii
and
methanosarcina mazei
