, 2010). Regulation

of rRNA transcription remains particularly cryptic, as most current approaches specifically exclude stable RNAs, including rRNA (e.g. Wurtzel et al., 2010). We used an SSV1-based find more reporter gene system in the model archaeon S. solfataricus (Jonuscheit et al., 2003) to determine whether the S. solfataricus core 16S/23S rRNA gene promoter (−41 to +1) is functional and regulated in vivo in response to the growth phase. The core TF55α and the wild-type lacS promoters from S. solfataricus were used as controls. Viral vector pKMSW72 containing the wild-type lacS gene in SSV1 was constructed in two steps (primers and plasmids listed in Table 1). First, the lacS gene plus 200 bp of upstream DNA was amplified from S. solfataricus P2 (DSM1617) DNA via PCR using Pfu DNA polymerase and primers BG840 and BG841, thereby introducing BamHI sites.

The BamHI-cut PCR product was ligated into similarly Talazoparib in vitro cut pUC28, yielding plasmid pKMSW70. Plasmid pKMSW70 was cut with PstI, dephosphorylated, and ligated to PstI-cut SSV1 to create pKMSW72 (Fig. 1). Vector pMAD107, containing the core 16S/23S rRNA gene promoter–lacS fusion, was constructed in three steps. First, the lacS promoter in pKMSW70 was deleting using long-inverse PCR (Clore & Stedman, 2007) using primers pKMSW70MasterF and pKMSW70MasterR. The PCR product was phosphorylated and ligated to produce pMT95. This plasmid was cut with PstI and PacI, dephosphorylated, and ligated to annealed oligonucleotides p16S/23SrRNAF and p16S/23SrRNAR. For annealing, oligonucleotides were incubated at 94 °C for 10 min followed by slow cooling to room temperature. The resulting plasmid, pMAD106, was digested with PstI, dephosphorylated, and ligated into SSV1 cut with PstI to yield

pMAD107. In the same RAS p21 protein activator 1 manner, primers pTF55αF and pTF55αR were annealed then ligated to pMT95 to produce the TF55α promoter-lacS construct pMAD109. This plasmid was inserted into PstI-cut SSV1 to create pMAD110. All constructions were confirmed by restriction endonuclease digestion and sequencing of the promoter and part of the lacS gene (data not shown). XL-10 Gold supercompetent Escherichia coli cells (Stratagene) were utilized for all steps in vector construction. The pMAD107, pMAD110, and pKMSW72 plasmids, purified from E. coli by alkaline lysis (Feliciello & Chinali 1993), were electroporated into S. solfataricus PH1 as described previously (Albers & Driessen, 2008). Successful transformation was confirmed by PCR using SSV1-specific primers UnivSSV#7F and UnivSSV#8R (Snyder et al., 2004) or B49F and B49R. For UnivSSV#7F and UnivSSV#8R, PCR conditions were as follows: 95 °C 1 min, then 35 cycles, 95 °C, 30 s, 46 °C, 30 s, 72 °C, 1 min, and then 7 min at 72 °C. For B49F and B49R, 95 °C 1 min, then 35 cycles, 95, 60, and 72 °C for 30 s each, then 4 min at 72 °C. Sulfolobus solfataricus strains were grown aerobically at 76 °C on plates or in liquid media, both as in Jonuscheit et al. (2003).