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Applied and Environmental Microbiology, April 1999, p. 1596-1602, Vol. 65, No. 4
Section of Molecular Genetics of Industrial
Micro-organisms,
Received 3 August 1998/Accepted 12 January 1999
Botrytis cinerea is a plant-pathogenic fungus infecting
over 200 different plant species. We use a molecular genetic approach to study the process of pectin degradation by the fungus. Recently, we
described the cloning and characterization of an endopolygalacturonase (endoPG) gene from B. cinerea (Bcpg1) which is
required for full virulence. Here we describe the cloning and
characterization of five additional endoPG-encoding genes from B. cinerea SAS56. The identity at the amino acid level between the
six endoPGs of B. cinerea varied from 34 to 73%.
Phylogenetic analysis, by using a group of 35 related fungal endoPGs
and as an outgroup one plant PG, resulted in the identification of five
monophyletic groups of closely related proteins. The endoPG proteins
from B. cinerea SAS56 could be assigned to three different
monophyletic groups. DNA blot analysis revealed the presence of the
complete endoPG gene family in other strains of B. cinerea,
as well as in other Botrytis species. Differential gene
expression of the gene family members was found in mycelium grown in
liquid culture with either glucose or polygalacturonic acid as the
carbon source.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Cloning and Partial Characterization of
Endopolygalacturonase Genes from Botrytis cinerea
*
Corresponding author. Mailing address: Section of
Molecular Genetics of Industrial Micro-organisms, Wageningen
Agricultural University, Dreijenlaan 2, 6703 HA Wageningen, The
Netherlands. Phone: 31-317-482865 or 31-317-484439. Fax: 31-317-484011. E-mail: office{at}algemeen.mgim.wau.nl.
Applied and Environmental Microbiology, April 1999, p. 1596-1602, Vol. 65, No. 4
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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