Previous Article | Next Article ![]()
Applied and Environmental Microbiology, January 2001, p. 363-370, Vol. 67, No. 1
Max-Planck-Institut für Molekulare
Pflanzenphysiologie, Am Mühlenberg 1, D-14476 Golm, Germany
Received 14 August 2000/Accepted 2 November 2000
We have purified a fructosyltransferase from conidia of the
inulin-producing fungus Aspergillus sydowi IAM 2544 and
obtained peptide sequences from proteolytic fragments of the protein.
With degenerated primers, we amplified a PCR fragment that was used to
screen a cDNA library. The fructosyltransferase gene from
Aspergillus sydowi (EMBL accession no. AJ289046) is
expressed in conidia, while no expression could be detected in mycelia
by Northern blot analysis of mycelial RNA. The gene encodes a protein
with a calculated molecular mass of 75 kDa that is different from all
fructosyltransferases in the databases. The only homology that could be
detected was to the invertase of Aspergillus niger (EMBL
accession no. L06844). The gene was functionally expressed in
Escherichia coli, yeast, and potato plants. With protein
extracts from transgenic bacteria and yeast, fructooligosaccharides
could be produced in vitro. In transgenic potato plants, inulin
molecules of up to 40 hexose units were synthesized in vivo. While in
vitro experiments with protein extracts from conidia of
Aspergillus sydowi yielded the same pattern of
oligosaccharides as extracts from transformed bacteria and yeast, in
vivo inulin synthesis with fungal conidia leads to the production of a
high-molecular-weight polymer.
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.1.363-370.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Gene Cloning and Functional Characterization by
Heterologous Expression of the Fructosyltransferase of
Aspergillus sydowi IAM 2544
*
Corresponding author. Mailing address:
Max-Planck-Institut für Molekulare Pflanzenphysiologie, Am
Mühlenberg 1, D-14476 Golm, Germany. Phone: 49-(0)331-5678251.
Fax: 49-(0)331-5678250. E-mail: heyer{at}mpimp-golm.mpg.de.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»