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Applied and Environmental Microbiology, June 2001, p. 2829-2832, Vol. 67, No. 6
Institute of Biotechnology, ETH
Hönggerberg, HPT, CH 8093, Zürich,
Switzerland,1 and Rhône
Poulenc-CRIT, 69153 Décines Charpieu cedex,
France2
Received 19 January 2001/Accepted 12 March 2001
The toluene-degrading strain Rhodococcus opacus PWD4
was found to hydroxylate D-limonene exclusively in the
6-position, yielding enantiomerically pure (+)
trans-carveol and traces of (+) carvone. This
biotransformation was studied using cells cultivated in chemostat culture with toluene as a carbon and energy source. The maximal specific activity of (+) trans-carveol formation was 14.7 U
(g of cells [dry weight])
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.6.2829-2832.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Biotransformation of D-Limonene to (+)
trans-Carveol by Toluene-Grown Rhodococcus opacus
PWD4 Cells
1, and the final yield was 94 to 97%. Toluene was found to be a strong competitive inhibitor of the
D-limonene conversion. Glucose-grown cells did not form any
trans-carveol from D-limonene. These results suggest that one of the enzymes involved in toluene degradation is
responsible for this allylic monohydroxylation. Another toluene degrader (Rhodococcus globerulus PWD8) had a
lower specific activity but was found to oxidize most of the formed
trans-carveol to (+) carvone, allowing for the biocatalytic
production of this flavor compound.
*
Corresponding author. Mailing address: Institute of
Biotechnology, ETH Hönggerberg, HPT, CH 8093, Zürich,
Switzerland. Phone: (41)-1-6333811. Fax: (41)-1-6331051. E-mail:
duetz{at}biotech.biol.ethz.ch.
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