An insertion mutant in this gene (atuR) expressed atu genes constitutively and the GCase protein was detected in cell extracts independent of the nature of the growth substrate (Fig. 1b). We conclude that atuR encodes a repressor of atu gene cluster expression and that inactivation Nutlin-3a nmr of atuR therefore results in a low, but constitutive expression of Atu proteins. If this assumption is true, AtuR should be able to specifically bind to the atuR-atuA intergenic sequence. The atuR gene was PCR amplified and cloned into

pET28a. The resulting construct, pSK3510, coded for an N-terminal his-tagged AtuR protein and was transformed into E. coli Rosetta 2 (DE3) pLysS RARE. Approximately 0.3 mg AtuR protein was purified from 800 mL

of an E. coli (pSK3510) LB culture (Fig. S2a). The quaternary structure of purified AtuR was analysed by analytical gel filtration on Superdex75. A value of 54±4 kDa was determined and suggested http://www.selleckchem.com/products/ganetespib-sta-9090.html that AtuR was present as a homodimer (26.9 kDa for monomer; Fig. S2b). The atuR-atuA intergenic region (280 bp) contains two perfect 13 bp inverted repeat sequences that are separated by a spacer sequence of 40 bp and are located immediately upstream of the ‘−10’ region of the atu gene cluster (Fig. 2). We speculated that this region could be important for atu gene cluster expression by acting as a potential binding site for AtuR protein. A 523-bp DNA fragment (DNA fragment #1) comprising the 5′-end of atuR

and the complete atuR-atuA intergenic region was PCR amplified and used as a binding substrate in EMSA. Figure 3a shows the EMSA results with different ratios of the atuR-atuA intergenic region and AtuR. The atuR-atuA intergenic region (DNA fragment #1) migrated with the expected size of ≈520 bp in a 6% polyacrylamide gel in the absence of AtuR (Fig. 3a, lane 6). A strong and complete shift of DNA fragment #1 towards higher apparent molecular masses (at the position of an ≈1000-bp DNA fragment) was observed when an eightfold or higher (10-fold) molar excess very of AtuR relative to the concentration of the atuR-atuA intergenic region was used (lanes 4 and 5 of Fig. 3a). Interestingly, lower amounts of AtuR (equal molar amount to twofold excess of AtuR relative to DNA fragment #1) resulted in the appearance of an intermediate shift (at an apparent position of ≈840 bp; Fig. 3a, lanes 1 and 2) in addition to the remaining unshifted DNA. This result indicates that the atuR-atuA intergenic region can bind different amounts of AtuR protein, resulting in different shift species. When a fourfold molar excess of AtuR was used, both shifted bands were obtained (at apparent 840 and 1000 bp. Fig. 3a, lane 3). Heat-inactivated AtuR (10 min, 95 °C) did not show any DNA-binding ability.