CAB15453) (Eppinger et al., 2011), the gene order of which is identical to that of TetR and PsmrAB. Our recent study showed that Bacillus species amount for 48% of culturable halophilic bacteria from soil samples around Daban Salt Lake (Wu et al., 2010). Therefore, it is the most possible that PsmrAB are the homolog of YvdSR pair in B. subtilis. The SMR protein family is a bacterial multidrug transporter family mainly including three

subclasses: the single-gene small multidrug pump, suppressor of GroEL mutation proteins (SUG) and PSMR family proteins (Bay et al., 2008). PSMR proteins are distinct from the other two subclasses of SMR proteins due to the requirement for simultaneous expression of both SMR homologs to confer a drug resistance phenotype (Bay et al., 2008). As shown in Fig. 3a, only the simultaneous presence of PsmrAB could confer AUY-922 E. coli KNabc NaCl resistance, indicating that selleck inhibitor PsmrAB should function as a heterodimer. The deduced amino sequence of PsmrA consists of 114 residues and that of PsmrB consists of 104 residues, which is consistent with the report that PSMR protein pairs generally consist of one protein with typical SMR protein length and a remaining protein that is longer (Bay et al., 2008). Topology analysis also showed that both PsmrA and PsmrB are composed of three transmembrane segments, respectively, which is also consistent with the

report that PSMR family proteins are usually integral membrane proteins containing three to four transmembrane segments (Bay et al., 2008). Therefore, PsmrAB should belong to PSMR protein family. Escherichia coli KAM3 lacking a restriction system and a main drug transporter AcrAB or E. coli DH5α and ethidium bromide, a representative of antimicrobial drugs, are usually used for the determination IMP dehydrogenase of PSMR family proteins (Jack et al., 2000; Masaoka et al.,

2000). In this study, when pEASY T3-psmrAB were introduced into E. coli DH5α, PsmrAB was found to only be able to slightly enhance the resistance of E. coli DH5α to chloramphenicol but not any other antimicrobials especially ethidium bromide (Table 1). However, no chaloramphenicol/H+ antiport activity was detected in everted membrane vesicles from KNabc/pEASY T3-psmrAB and KNabc/pEASY T3 (data not shown). In B. subtilis, both of EbrAB (Bay et al., 2008), YkkCD (Masaoka et al., 2000) and YvaE of the YvaDE pair were characterized to be able to confer host drug resistance phenotype (Jack et al., 2000). However, neither protein of YvdSR pair could confer a drug resistance phenotype when expressed as single genes or in tandem (Chung & Sair, 2001). As it is most possible that PsmrAB are the homolog of YvdSR pair, PsmrAB cannot function as a MDR-type drug transporter just like YvdSR pair. Therefore, future studies must confirm whether YvdSR pair can also exactly exhibit Na+/H+ antiporter activity.