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Volume 270,
Number 45,
Issue of November 10, 1995 pp. 27172-27178
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Molecular
Cloning and Characterization of a Rhamnogalacturonan Acetylesterase
from Aspergillus aculeatus SYNERGISM BETWEEN RHAMNOGALACTURONAN DEGRADING ENZYMES
(Received for publication, March 14,
1995; and in revised form, July 17, 1995)
Sakari
Kauppinen ,
Stephan
Christgau,
Lene V.
Kofod ,
Torben
Halkier ,
Kurt
Dörreich ,
Henrik
Dalbøge
A rhamnogalacturonan acetylesterase (RGAE) was purified to
homogeneity from the filamentous fungus Aspergillus aculeatus,
and the NH -terminal amino acid sequence was determined.
Full-length cDNAs encoding the enzyme were isolated from an A.
aculeatus cDNA library using a polymerase chain reaction-generated
product as a probe. The 936-base pair rha1 cDNA encodes a
250-residue precursor protein of 26,350 Da, including a 17-amino acid
signal peptide. The rha1 cDNA was overexpressed in Aspergillus oryzae, a filamentous fungus that does not possess
RGAE activity, and the recombinant enzyme was purified and
characterized. Mass spectrometry of the native and recombinant RGAE
revealed that the enzymes are heterogeneously glycosylated. In
addition, the observed differences in their molecular masses, lectin
binding patterns, and monosaccharide compositions indicate that the
glycan moieties on the two enzymes are structurally different. The RGAE
was shown to act in synergy with rhamnogalacturonase A as well as
rhamnogalacturonase B from A. aculeatus in the degradation of
apple pectin rhamnogalacturonan. RNA gel blot analyses indicate that
the expression of rhamnogalacturonan degrading enzymes by A.
aculeatus is regulated at the level of transcription and is
subjected to carbon catabolite repression by glucose.

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Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
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