CyaC inclusions were completely dissolved in 8 M urea at 37 °C for 1 h (Fig. 2b, lane 1). A fast removal of urea in the refolding step

using a reciprocal dialysis or a high dilution (10–100-fold) of the unfolded CyaC solution resulted in a large fraction (≥80%) of sediment aggregates. It has been shown Natural Product Library chemical structure that certain aggregation suppressors (e.g. NaCl) added to the refolding solution at an intermediate-denaturant concentration can induce denatured proteins to refold into globular shape favoring a native conformation (Lairez et al., 2003). Herein, one-step reduction of urea to an intermediate concentration (2 M) of the denatured CyaC solution supplemented with 150 mM NaCl was found to recover a high proportion of refolded monomers (Fig. 2b, lane 2) as observed by size-exclusion chromatography. Thus, this cardinal step allowed us finally to obtain the urea-free refolded CyaC protein with ∼90% purity and ∼70% yield recovery

(∼70 mg L−1 of culture) as analyzed by SDS-PAGE (Fig. 2b, lane 3). It should be noted that the 21-kDa purified proteins obtained from both soluble and insoluble fractions were reverified to be CyaC-acyltransferase as their part of trypsin-generated peptide sequence (DWPVHLLARNTLAPIQLGQYILLR) analyzed by LC/MS/MS, perfectly matching the corresponding CyaC sequence (residues Asp35-Arg58). As mentioned earlier, the CyaA-PF fragment (Fig. 1b, lane 2) can be acylated AZD0530 ic50 in vivo by coexpressed CyaC to exhibit hemolytic activity (Powthongchin & Angsuthanasombat, 2008). By this activation analogy, we initially used this fragment as an acylated target for testing the activating activity of CyaC. When the cell lysate containing proCyaA-PF (Fig. 1b, lane 1) was mixed with the purified CyaC protein,

it showed high hemolytic activity against sheep erythrocytes (∼30%). In contrast, the lysate containing proCyaA-PF alone or the proCyaA-PF-free lysate mixed with CyaC exhibited very weak activity (≤5%) (Table 1). These results indicate that the proCyaA-PF fragment could be acylated by CyaC in vitro. It was also observed that both soluble and refolded CyaC could activate the proCyaA-PF fragment in vitro to show comparable hemolysis of ∼30%, suggesting that the refolded CyaC is likely to exist as an active monomer corresponding to the native-folded protein in soluble fraction. Thus, C59 supplier this hemolytic activity could be inferred as the CyaC capability in transferring acyl group to the proCyaA-PF acceptor. Further attempts were therefore made to assay its catalyzing capability of acyl group, as this has not been characterized thus far for any RTX-acyltransferases. It has been shown that homoserine acyltransferase (Ziegler et al., 2007) and arylamine N-acetyltransferase (Pluvinage et al., 2007) also catalyze a related reaction in vitro– namely, the hydrolysis of oxygen–ester bond of a nonphysiological substrate (i.e. pNPA).