, 1997). Tagged termini might influence binding and postbinding processes of TDH and could be an explanation for the weaker hemolytic activity of tagged proteins. One disulfide bridge is formed in the subunits (Tsunasawa et al., 1987 and Nishibuchi et al., 1989), however, the disulfide bond is possibly not important for hemolytic activity of TDH (Baba et al., 1992 and Yanagihara et al., 2010). It has been shown that forming of disulfide bonds is generally possible in a simple batch reaction of the E. coli based cell-free protein synthesis system ( Kim and Swartz, 2004). The addition selleck screening library of tags offers a great advantage for the

purification of the toxin and its further application, therefore we decided to analyze the toxin variant synthesized with an additional

C-terminal His-tag more intensively. His-tagged toxins were purified using His-tag Dynabeads®. Selleck Dabrafenib Aliquots of CRMs and purified toxin derivatives were loaded on SDS-PAGE and transferred to nitrocellulose membrane after electrophoresis (Fig. 7). The Western Blot revealed again that only one protein was synthesized when the DNA construct encoding preTDH-His (protein band I, Fig. 7B lane 1) was used as a template, whereas from the PCR product encoding mTDH-His two His-tagged proteins were produced (bands II and III in lane 2). This result was also visible after purification with His-tag Dynabeads® (lanes 3 and 4). The purified His-tagged mTDH displayed hemolytic activity as did the unpurified TDH from the supernatant fraction (data not shown). To confirm the identities of the cell free expressed TDH proteins, three protein bands were excised from SDS-PAGE gels and subjected to tryptic in-gel digestion followed by tandem MALDI-TOF mass spectrometry (MS/MS) protein identification. Protein database searches for band I retrieved thermostable direct hemolysin A (TDH2) of O3:K6 reference strain V. parahaemolyticus RIMD 2210633. MALDI-TOF MS/MS spectrometry analysis revealed two diagnostic peaks corresponding to peptides DTTFNTNAPVNVEVSDFWTNR (m/z 2427.1) and SDQVQLQHSYDSVANFVGEDEDSIPSK

(m/z 2994.4) (see Suppl. Fig. S2). The same peaks were found in band II. Interestingly, Carnitine palmitoyltransferase II the peak at m/z 2994.4 was missing in the MS analysis of band III, but instead a peak at m/z 2877.6 was observed, which is diagnostic for thermostable direct hemolysin S (TDH1) of V. parahaemolyticus from RIMD 2210633 and corresponds to peptide SGQVQLQHSYNSVANFVGEDEGSIPSK. This peptide contains three amino acid exchanges compared to the corresponding sequence in TDH2, which could be confirmed by MALDI-TOF MS/MS analyses. Thus we concluded that protein I corresponded to the preprotein of TDH2 containing the signal peptide, while proteins II and III were derived from the chromosomal genes tdh1 and tdh2 lacking the sequence encoding the signal peptide. As shown above, two proteins were synthesized when primers containing gene specific sequences for the mature toxins were used.