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J Bacteriol, March 1998, p. 1103-1109, Vol. 180, No. 5
Department of Animal Sciences, University of
Kentucky, Lexington, Kentucky 40546-0215
Received 18 August 1997/Accepted 23 December 1997
The genes encoding xylose isomerase (xylA) and xylulose
kinase (xylB) from the thermophilic anaerobe
Thermoanaerobacter ethanolicus were found to constitute an
operon with the transcription initiation site 169 nucleotides upstream
from the previously assigned (K. Dekker, H. Yamagata, K. Sakaguchi, and
S. Udaka, Agric. Biol. Chem. 55:221-227, 1991) promoter region. The
bicistronic xylAB mRNA was processed by cleavage within the
5'-terminal portion of the XylB-coding sequence. Transcription of
xylAB was induced in the presence of xylose, and, unlike in
all other xylose-utilizing bacteria studied, was not repressed by
glucose. The existence of putative xyl operator sequences
suggested that xylose utilization is controlled by a repressor-operator
mechanism. The T. ethanolicus xylB gene coded for a
500-amino-acid-residue protein with a deduced amino acid sequence
highly homologous to those of other XylBs. This is the first report of
an xylB nucleotide sequence and an xylAB operon
from a thermophilic anaerobic bacterium.
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Cloning and Characterization of Transcription of
the xylAB Operon in Thermoanaerobacter
ethanolicus
*
Corresponding author. Mailing address: 212 W. P. Garrigus Building, Department of Animal Sciences, University of
Kentucky, Lexington, KY 40546-0215. Phone: (606) 257-7554. Fax: (606)
257-5318. E-mail: strobel{at}pop.uky.edu.
Published with the approval of the Director of the Kentucky
Agricultural Experiment Station as journal article no. 98-07-12.
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