ABSTRACT Selection of possible targets for vaccine and drug development requires an understanding of the physiology of bacterial pathogens, for which the ability to manipulate expression of essential genes is critical. For Streptococcus pyogenes (the group A streptococcus [GAS]), an important human pathogen, the lack of genetic tools for such studies has seriously hampered research. To address this problem, we characterized variants of the inducible P _tet cassette, in both sense and antisense contexts, as tools to regulate transcription from GAS genes. We found that although the three-operator P _tet construct [P _tet (O) ₃ ] had low uninduced expression, its induction level was low, while the two-operator construct [P _tet (O) ₂ ] was inducible to a high level but showed significant constitutive expression. Use of P _tet (O) ₃ in the chromosome allowed us to demonstrate previously that RNases J1 and J2 are required for growth of GAS. Here we report that the uninduced level from the chromosomally inserted P _tet (O) ₂ construct was too high for us to observe differential growth. For the highly expressed histone-like protein (Hlp) of GAS, neither chromosomal insertion of P _tet (O) ₂ or P _tet (O) ₃ nor their use on a high-copy-number plasmid to produce antisense RNA specific to hlp resulted in adequate differential expression. However, by replacing the ribosome binding site of hlp with an engineered riboswitch to control translation of Hlp, we demonstrated for the first time that this protein is essential for GAS growth.