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Journal of Bacteriology, March 2003, p. 1768-1775, Vol. 185, No. 6
0021-9193/03/$08.00+0     DOI: 10.1128/JB.185.6.1768-1775.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Roles of the Enantioselective Glutathione S-Transferases in Cleavage of ß-Aryl Ether

Department of Bioengineering, Nagaoka University of Technology, Nagaoka, Niigata 940-2188,¹ Graduate School of Bio-Applications and Systems Engineering, Tokyo University of Agriculture and Technology, Koganei, Tokyo 184-8588, Japan²

Received 12 August 2002/ Accepted 11 December 2002

Cleavage of the ß-aryl ether linkage is the most important process in lignin degradation. Here we characterize the three tandemly located glutathione S-transferase (GST) genes, ligF, ligE, and ligG, from low-molecular-weight lignin-degrading Sphingomonas paucimobilis SYK-6, and we describe the actual roles of these genes in the ß-aryl ether cleavage. Based on the identification of the reaction product by electrospray ionization-mass spectrometry, a model compound of ß-aryl ether, -(2-methoxyphenoxy)-ß-hydroxypropiovanillone (MPHPV), was transformed by LigF or LigE to guaiacol and -glutathionyl-ß-hydroxypropiovanillone (GS-HPV). This result suggested that LigF and LigE catalyze the nucleophilic attack of glutathione on the carbon atom at the ß position of MPHPV. High-pressure liquid chromatography-circular dichroism analysis indicated that LigF and LigE each attacked a different enantiomer of the racemic MPHPV preparation. The ligG gene product specifically catalyzed the elimination of glutathione from GS-HPV generated by the action of LigF. This reaction then produces an achiral compound, ß-hydroxypropiovanillone, which is further degraded by this strain. Disruption of the ligF, ligE, and ligG genes in SYK-6 showed that ligF is essential to the degradation of one of the MPHPV enantiomers, and the alternative activities which metabolize the substrates of LigE and LigG are present in this strain.

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