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Journal ArticleDOI

Intraspecific variability and exopolysaccharide production in Aureobasidium pullulans.

TLDR
The UP-PCR technique revealed a greater degree of heterogeneity between the groups studied, and PCR-ribotyping with AluI and MspI is sufficient for analysis of distance between populations.
Abstract
Forty seven strains of the black yeasts, Aureobasidium pullulans and Hormonema dematioides, and the type strain of Hormonema macrosporum were examined using PCR-ribotyping and universally primed PCR with subsequent hybridization. Four groups (populations) were distinguished within A. pullulans with PCR-ribotyping, which largely coincided with UP-PCR/hybridization groups. The UP-PCR technique revealed a greater degree of heterogeneity between the groups studied. Five strains identified as Hormonena dematioides on the basis of physiological and morphological data formed a group recognizable with PCR-ribotyping and UP-PCR/hybridization, which also included H. macrosporum. Aureobasidium pullulans is characterized by the absence of RsaI restriction sites in rDNA amplified with primers 5.8S-R and LR7, while Hormonema species possessed several bands after RsaI digestion. For analysis of distance between populations, PCR-ribotyping with AluI and MspI is sufficient. Strains of A. pullulans produce exopolysaccharides in liquid media with different nitrogen sources, while the strains of Hormonema synthesize minor amounts of polysaccharides in media with peptone. Populations of A. pullulans differ slightly from each other in their optimal, medium-dependent production of polysaccharides.

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Journal ArticleDOI

Redefinition of Aureobasidium Pullulans and Its Varieties

TL;DR: To characterise the genetic variability of Aureobasidium pullulans strains originating from the Arctic and strains originating pan-globally, a multilocus molecular analysis was performed and a partial elongase-encoding gene was successfully used as a phylogenetic marker at the (infra-)specific level.
Journal ArticleDOI

One stop mycology

TL;DR: This listing covers the period May 1, 1997 through to June 30, 1997, which roughly corresponds with the British Mycological Society's Special Interest Committees.
Journal ArticleDOI

Control of postharvest rots of sweet cherries and table grapes with endophytic isolates of Aureobasidium pullulans

TL;DR: In this paper, endophytic isolates of Aureobasidium pullulans were obtained from the flesh of sweet cherries and extensively screened to evaluate their biocontrol activity against postharvest rots.
Book ChapterDOI

Black Yeasts and Meristematic Fungi: Ecology, Diversity and Identification

TL;DR: For the morphological classification of the fungi discussed in this chapter three terms are used in the literature with overlapping meaning: black yeasts, meristematic fungi and microcolonial fungi (MCF).
Journal ArticleDOI

Genetic diversity and biocontrol activity of Aureobasidium pullulans isolates against postharvest rots

TL;DR: Random amplified polymorphic DNA technique (RAPD) was a useful method for the identification and evaluation of the survival rate of the applied antagonist in Aureobasidium pullulans.
References
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Journal Article

PHYLIP-Phylogeny inference package (Version 3.2)

J. Felsenstein
- 01 Jan 1989 - 
Journal ArticleDOI

DNA polymorphisms amplified by arbitrary primers are useful as genetic markers

TL;DR: A new DNA polymorphism assay based on the amplification of random DNA segments with single primers of arbitrary nucleotide sequence is described, suggesting that these polymorphisms be called RAPD markers, after Random Amplified Polymorphic DNA.
Journal ArticleDOI

Fingerprinting genomes using PCR with arbitrary primers

TL;DR: The generality of the arbitrarily primed PCR method is demonstrated by application to twenty four strains from five species of Staphylococcus, eleven strains of Streptococcus pyogenes and three varieties of Oryza sativa.
Journal ArticleDOI

Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species.

TL;DR: A novel approach that uses the polymerase chain reaction (PCR) for rapid simplified restriction typing and mapping of DNA from many different isolates is described, which ought to have wide applicability for clinical detection and other studies.
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