Title : Substantially improving the enantioconvergence of PvEH1, a Phaseolus vulgaris epoxide hydrolase, towards m-chlorostyrene oxide by laboratory evolution - Zong_2019_Microb.Cell.Fact_18_202 |
Author(s) : Zong XC , Li C , Xu YH , Hu D , Hu BC , Zang J , Wu MC |
Ref : Microb Cell Fact , 18 :202 , 2019 |
Abstract :
BACKGROUND: Epoxide hydrolase can regioselectively catalyze the oxirane ring-opening hydrolysis of rac-epoxides producing the corresponding chiral diols. In our laboratory, a gene named pveh1 encoding an EH from Phaseolus vulgaris was cloned. Although the directed modification of PvEH1 was carried out, the mutant PvEH1(Y3) showed a limited degree of enantioconvergence towards racemic (rac-) m-chlorostyrene oxide (mCSO). RESULTS: PvEH1 and PvEH1(Y3) were combinatively subjected to laboratory evolution to further enhance the enantioconvergence of PvEH1(Y3) towards rac-mCSO. Firstly, the substrate-binding pocket of PvEH1 was identified using a CAVER 3.0 software, and divided into three zones. After all residues in zones 1 and 3 were subjected to leucine scanning, two E. coli transformants, E. coli/pveh1(Y149L) and /pveh1(P184L), were selected, by which rac-mCSO was transformed into (R)-m-chlorophenyl-1,2-ethanediol (mCPED) having 55.1% and 27.2% ee(p). Secondly, two saturation mutagenesis libraries, E. coli/pveh1(Y149X) and /pveh1(P184X) (X: any one of 20 residues) were created at sites Y149 and P184 of PvEH1. Among all transformants, both E. coli/pveh1(Y149L) (65.8% alpha(S) and 55.1% ee(p)) and /pveh1(P184W) (66.6% alpha(S) and 59.8% ee(p)) possessed the highest enantioconvergences. Finally, the combinatorial mutagenesis was conducted by replacements of both Y149L and P184W in PvEH1(Y3), constructing E. coli/pveh1(Y3Z2), whose alpha(S) reached 97.5%, higher than that (75.3%) of E. coli/pveh1(Y3). In addition, the enantioconvergent hydrolysis of 20 mM rac-mCSO was performed by E. coli/pveh1(Y3Z2), giving (R)-mCPED with 95.2% ee(p) and 97.2% yield. CONCLUSIONS: In summary, the enantioconvergence of PvEH1(Y3Z2) was successfully improved by laboratory evolution, which was based on the study of substrate-binding pocket by leucine scanning. Our present work introduced an effective strategy for the directed modification of enantioconvergence of PvEH1. |
PubMedSearch : Zong_2019_Microb.Cell.Fact_18_202 |
PubMedID: 31739786 |
Gene_locus related to this paper: phavu-PvEH1 |
Gene_locus | phavu-PvEH1 |
Zong XC, Li C, Xu YH, Hu D, Hu BC, Zang J, Wu MC (2019)
Substantially improving the enantioconvergence of PvEH1, a Phaseolus vulgaris epoxide hydrolase, towards m-chlorostyrene oxide by laboratory evolution
Microb Cell Fact
18 :202
Zong XC, Li C, Xu YH, Hu D, Hu BC, Zang J, Wu MC (2019)
Microb Cell Fact
18 :202