Paralogous gene analysis reveals a highly enantioselective 1,2‐O‐isopropylideneglycerol caprylate esterase of Bacillus subtilis

Carboxylesterase NP of Bacillus subtilis Thai I‐8, characterized in 1992 as a very enantioselective (S)‐naproxen esterase, was found to show no enantiopreference towards (S)‐1,2‐O‐isopropylideneglycerol (IPG) esters. The ybfK gene was identified by the B. subtilis genome project as an unknown gene w...

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Veröffentlicht in:European journal of biochemistry 2001-06, Vol.268 (11), p.3332-3338
Hauptverfasser: Dröge, Melloney J., Bos, Rein, Quax, Wim J.
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Sprache:eng
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Zusammenfassung:Carboxylesterase NP of Bacillus subtilis Thai I‐8, characterized in 1992 as a very enantioselective (S)‐naproxen esterase, was found to show no enantiopreference towards (S)‐1,2‐O‐isopropylideneglycerol (IPG) esters. The ybfK gene was identified by the B. subtilis genome project as an unknown gene with homology to carboxylesterase NP. The purpose of the present study was to characterize the ybfK gene product in order to determine whether this paralogue of carboxylesterase NP had an altered or enhanced stereospecificity. The ybfK gene was cloned and expressed in B. subtilis using a combination of two strong promoters in a multicopy vector. The enzyme was purified from the cytoplasm of B. subtilis by means of anion exchange and hydrophobic interaction chromatography. The purified YbfK is an enzyme of 296 amino acids and shows an apparent molecular mass of 32 kDa (SDS/PAGE). Comparison of the activities of YbfK and carboxylesterase NP towards caprylate esters of IPG revealed that YbfK produces (S)‐IPG with 99.9% enantioselectivity. Therefore, we conclude that we have isolated a paralogue of carboxylesterase NP that can be used for the enantioselective production of (S)‐IPG.
ISSN:0014-2956
1432-1033
DOI:10.1046/j.1432-1327.2001.02238.x