Yersinia enterocolitica and Photorhabdus asymbiotica [beta]-lactamases BlaA are exported by the twin-arginine translocation pathway

In general, [beta]-lactamases of medically important Gram-negative bacteria are Sec-dependently translocated into the periplasm. In contrast, [beta]-lactamases of Mycobacteria spp. (BlaC, BlaS) and the Gram-negative environmental bacteria Stenotrophomonas maltophilia (L2) and Xanthomonas campestris (BlaXCC-1) have been reported to be secreted by the twin-arginine translocation (Tat) system. Yersinia enterocolitica carries 2 distinct [beta]-lactamase genes (blaA and blaB) encoding BlaAYe and the AmpC-like [beta]-lactamase BlaB, respectively. By using the software PRED-TAT for prediction and discrimination of Sec from Tat signal peptides, we identified a functional Tat signal sequence for Yersinia BlaAYe. The Tat-dependent translocation of BlaAYe could be clearly demonstrated by using a Y. enterocolitica tatC-mutant and cell fractionation. Moreover, we could demonstrate a unique unusual temperature-dependent activity profile of BlaAYe ranging from 15 to 60 degree C and a high amelting temperaturea (TM = 44.3 degree ) in comparison to the related Sec-dependent [beta]-lactamase TEM-1 (20a50 degree C, TM = 34.9 degree C). Strikingly, the blaA gene of Y. enterocolitica is present in diverse environmental Yersinia spp. and a blaA homolog gene could be identified in the closely related Photorhabdus asymbiotica (BlaAPa; 69% identity to BlaAYe). For BlaAPa of P. asymbiotica, we could also demonstrate Tat-dependent secretion. These results suggest that Yersinia BlaA-related [beta]-lactamases may be the prototype of a large Tat-dependent [beta]-lactamase family, which originated from environmental bacteria.