Rasool_2005_FEMS.Microbiol.Lett_249_113

Reference

Title : Molecular cloning of enantioselective ester hydrolase from Bacillus pumilus DBRL-191 - Rasool_2005_FEMS.Microbiol.Lett_249_113
Author(s) : Rasool S , Johri S , Riyaz-Ul-Hassan S , Maqbool QU , Verma V , Koul S , Taneja SC , Qazi GN
Ref : FEMS Microbiology Letters , 249 :113 , 2005
Abstract :

A gene from Bacillus pumilus expressed under its native promoter was cloned in Escherichia coli. Recombinant B. pumilus esterase (BPE) affects the kinetic resolution of racemic mixtures such as unsubstituted and substituted 1-(phenyl)ethanols (E approximately 33-103), ethyl 3-hydroxy-3-phenylpropanoate (E approximately 45-71), trans-4-fluorophenyl-3-hydroxymethyl-N-methylpiperidine (E approximately 10-13) and ethyl 2-hydroxy-4-phenylbutyrate (E approximately 7). The enzyme is composed of a 34-amino acid signal peptide and a 181-amino acid mature protein corresponding to a molecular weight of approximately 19.2kD and pI approximately 9.4. 3-D the structural model of the enzyme built by homology modelling using the atomic coordinates from the crystal structure of B. subtilis lipase (LipA) showed a compact minimal alpha/beta hydrolase fold.

PubMedSearch : Rasool_2005_FEMS.Microbiol.Lett_249_113
PubMedID: 16006072

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Citations formats

Rasool S, Johri S, Riyaz-Ul-Hassan S, Maqbool QU, Verma V, Koul S, Taneja SC, Qazi GN (2005)
Molecular cloning of enantioselective ester hydrolase from Bacillus pumilus DBRL-191
FEMS Microbiology Letters 249 :113

Rasool S, Johri S, Riyaz-Ul-Hassan S, Maqbool QU, Verma V, Koul S, Taneja SC, Qazi GN (2005)
FEMS Microbiology Letters 249 :113