Pennapa Manitchotpisit1, Timothy D. Leathers2, Xin-Liang Li2, Cletus P. Kurtzman2, Douglas E. Eveleigh3, Sehanat Prasongsuk4, and Hunsa Punnapayak4. (1) Plant Biomass Utilization Research Unit, Department of Botany, Chulalongkorn University, Payathai Road, Pathumwan, Bangkok, Thailand, (2) USDA-ARS-NCAUR, 1815 N University, Peoria, IL 61604, (3) Department of Biochemistry and Microbiology, Rutgers University, School of Environmental and Biological Sciences, Lipman Hall, 76 Lipman Drive, New Brunswick, NJ 08901, (4) Plant Biomass Utilization Research Unit, Department of Botany, Faculty of Science, Chulalongkorn University, Payathai Road, Pathumwan, Bangkok, Thailand
The polymorphic fungus
Aureobasidium pullulans was isolated from many provinces in tropical
Thailand and cultured in pullulan production medium (PM)
containing sucrose and peptone as carbon and nitrogen sources, respectively. Liquid PM cultures varied in color from cream to pale pink, light burgundy red, light brown, olivaceous green, and black. Most isolates produced colonies that were smooth, moist, and cream or pale pink on yeast malt agar (YMA) medium.
Molecular sequence analyses of the internal transcribed spacer (ITS) regions of rDNA showed no differences among these isolates. However, the intergenic spacer (IGS) regions of rDNA revealed the possibility of strain differences. Preliminary data from 9 isolates suggest that IGS-PCR patterns cluster in groups according to color variability. Sequence analysis of 3-4 Kb of IGS1 and IGS2 showed similarities among isolates consistent with the IGS-PCR patterns.