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Journal of Bacteriology, September 1998, p. 4387-4391, Vol. 180, No. 17
Institut für Mikrobiologie,
Westfälische Wilhelms-Universität Münster, D-48149
Münster, Germany
Received 25 March 1998/Accepted 7 June 1998
The coniferyl aldehyde dehydrogenase (CALDH) of
Pseudomonas sp. strain HR199 (DSM7063), which catalyzes the
NAD+-dependent oxidation of coniferyl aldehyde to ferulic
acid and which is induced during growth with eugenol as the carbon
source, was purified and characterized. The native protein exhibited an apparent molecular mass of 86,000 ± 5,000 Da, and the subunit mass was 49.5 ± 2.5 kDa, indicating an
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Purification and Characterization of the Coniferyl
Aldehyde Dehydrogenase from Pseudomonas sp. Strain HR199 and
Molecular Characterization of the Gene
2 structure
of the native enzyme. The optimal oxidation of coniferyl aldehyde to
ferulic acid was obtained at a pH of 8.8 and a temperature of 26°C.
The Km values for coniferyl aldehyde and
NAD+ were about 7 to 12 µM and 334 µM, respectively.
The enzyme also accepted other aromatic aldehydes as substrates,
whereas aliphatic aldehydes were not accepted. The
NH2-terminal amino acid sequence of CALDH was determined in
order to clone the encoding gene (calB). The corresponding
nucleotide sequence was localized on a 9.4-kbp EcoRI
fragment (E94), which was subcloned from a Pseudomonas sp. strain HR199 genomic library in the cosmid pVK100. The partial sequencing of this fragment revealed an open reading frame of 1,446 bp
encoding a protein with a relative molecular weight of 51,822. The
deduced amino acid sequence, which is reported for the first time for a
structural gene of a CALDH, exhibited up to 38.5% amino acid identity
(60% similarity) to NAD+-dependent aldehyde dehydrogenases
from different sources.
*
Corresponding author. Mailing address: Institut
für Mikrobiologie, Westfälische Wilhelms-Universität
Münster, Corrensstraße 3, D-48149 Münster, Germany. Phone:
49-251-8339829. Fax: 49-251-8338388. E-mail:
priefer{at}uni-muenster.de.
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