Journal of Bioscience and Bioengineering 2010-01-01

Biocatalytic resolution of glycidyl phenyl ether using a novel epoxide hydrolase from a marine bacterium,Rhodobacterales bacteriumHTCC2654

Jung-Hee Woo, Ji-Hyun Kang, Young-Ok Hwang, Jang-Cheon Cho, Sang-Jin Kim, Sung Gyun Kang, Jung-Hee Woo, Ji-Hyun Kang, Young-Ok Hwang, Jang-Cheon Cho, Sang-Jin Kim, Sung Gyun Kang

Index: J. Biosci. Bioeng. 109(6) , 539-44, (2010)

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Abstract

As a continuous effort of developing highly enantioselective epoxide hydrolase from marine microorganisms, it was found that Rhodobacterales bacterium HTCC2654 was highly enantioselective toward racemic glycidyl phenyl ether (GPE). An open reading frame (ORF) encoding a putative epoxide hydrolase (EHase) was cloned from the genome of R. bacterium HTCC2654, followed by expression and purification in Escherichia coli. The purified EHase (REH) hydrolyzed ( S)-GPE preferentially over ( R)-GPE. Enantiopure ( R)-GPE from kinetic resolution of 29.2 mM racemic GPE using the purified REH could be obtained with enantiopurity of more than 99.9% enantiomeric excess (ee) and 38.4% yield (theoretical, 50%) within 20 min (enantiomeric ratio ( E-value): 38.4). The enantioselective activity of REH toward GPE was also confirmed by the analysis of the vicinal diol, 3-phenoxy-1,2-propanediol. To our knowledge, this study demonstrates the highest enantioselective resolution of racemic GPE using a purified biocatalyst among the known native EHases.