Aureobasidium pullulans
(de Bary & Löwenthal) G.Arnaud · speciesAt a glance
Sources11 archives
Databases and archives Aureobasidium pullulans's data was compiled from.
WikipediaWikimedia Foundation7 languages↗
BioWikiNetmultilingual Wikipediamultilingual↗
GBIFGlobal Biodiversity Information Facility1 183 records↗
OBISOcean Biodiversity Information System540 records↗
ENAEuropean Nucleotide Archive · EMBL-EBI5 732 eDNA detections↗
BOLD SystemsCentre for Biodiversity Genomics278 specimens↗
NCBIUS National Library of Medicinesequences↗
LOTUSNatural Products (Wikidata)compounds↗
Open Tree of LifeOpenTreephylogeny backbone↗
GoaTGenomes on a Tree · Sangergenome & karyotype↗
GLoBIGlobal Biotic Interactionsbiotic interactions↗Every layer below draws on the sources above — open one to explore it, or use ← → to move between tabs.
Aureobasidium pullulans is a ubiquitous and generalistic black, yeast-like fungus that can be found in different environments (e.g. soil, water, air and limestone). It is well known as a naturally occurring epiphyte or endophyte of a wide range of plant species (e.g. apple, grape, cucumber, green beans, cabbage) without causing any symptoms of disease. A. pullulans has a high importance in biotechnology for the production of different enzymes, siderophores and pullulan. Furthermore, A. pullulans is used in biological control of plant diseases, especially storage diseases. Chronic human exposure to A. pullulans via humidifiers or air conditioners can lead to hypersensitivity pneumonitis (extrinsic allergic alveolitis) or "humidifier lung". This condition is characterized acutely by dyspnea, cough, fever, chest infiltrates, and acute inflammatory reaction. The condition can also be chronic, and lymphocyte-mediated. The chronic condition is characterized radiographically by reticulonodular infiltrates in the lung, with apical sparing. The strains causing infections in humans were reclassified to A. melanogenum. A. pullulans can be cultivated on potato dextrose agar, where it produces smooth, faint pink, yeast-like colonies covered with a slimy mass of spores. Older colonies change to black due to chlamydospore production. Primary conidia are hyaline, smooth, ellipsoidal, one-celled, and variable in shape and size; secondary conidia are smaller. Conidiophores are undifferentiated, intercalary or terminal, or arising as short lateral branches. Endoconidia are produced in an intercalary cell and released into a neighboring empty cell. Hyphae are hyaline, smooth, and thinwalled, with transverse septa. The fungus grows at 10–35 °C with optimum growth at 30 °C. A. pullulans is notable for its phenotypic plasticity. Colony morphology may be affected by carbon source, colony age, temperature, light and substrate, with colonies ranging from homogeneous to sectored, yeast-like to filamentous growth, and from small to large. These changes, potentially influenced by epigenetic factors, and the particular developmental sequences that the colonies proceed through may be observed with the naked eye. Besides these morphological plasticity A. pullulans is also adaptable to various stressful conditions: hypersaline, acidic and alkaline, cold, and oligotrophic. Therefore, it is considered to be polyextremotolerant. The morphology-based taxonomy of the species is complicated by the large morphological variability between strains and even within a single strain. Based on molecular analyses, four varieties of the species A. pullulans were recognised: var. pullulans from substrates with low water activity and the phyllosphere and a variety of other habitats; var. melanogenum from aquatic habitats; var. subglaciale from glacial habitats; and var. namibiae, which was described on the basis of only one strain isolated from dolomitic marble in Namibia. However, when the genome sequences of these varieties became available, the differences between them were considered as too large to be accommodated in a single species. Therefore, the varieties were reclassified as new species: A. pullulans, A. melanogenum, A. subglaciale, and A. namibiae. The genome of A. pullulans s. str. contains large numbers of genes of gene families that can be linked to the nutritional versatility of the species and its stress tolerance. The genome also contains a homothallic mating-type locus. Further genome sequencing of fifty A. pullulans s. str. strains showed that the population of the species is homogeneous, with high levels of recombination and good dispersal. The species A. pullulans was thus recognised as a true generalist, able to inhabit a wide variety of habitats with no specialization to any of these habitats at the genomic level. Despite the presence in the genome of a putative mating locus, and the observation of high recombination rates, no sexual cycle has yet been reported in this organism. Due to the relatively recent redefinition of the species, most published work does not yet distinguish between the new species belonging to the previously recognised A. pullulans species complex. It is therefore not clear to what extent this knowledge is valid for A. pullulans s. str. and what should be attributed to the three new species.
No narrative description available for this taxon yet.
No structured trait data for this taxon yet.
Compounds documented for Aureobasidium pullulans across natural-product and food-composition databases — not just the ~150 nutrients on a classic label ("nutritional dark matter").
Compound class profile5 classes
Documented compounds41 total
| Compound | Class | Amount | Source |
|---|---|---|---|
| (3R,5R)-3,5-dihydroxydecanoic Acid | present | LOTUS | |
| (3R,5R)-3-(((3R,5R)-3,5-dihydroxy decanoyl)oxy)-5-hydroxydecanoic acid | present | LOTUS | |
| (3R,5R)-3-(((3R,5R)-5-(((3R,5R)-3,5-dihydroxydecan oyl)oxy)-3-hydroxydecanoyl)oxy)-5-hydroxydecanoic acid | present | LOTUS | |
| 3-[(5-Acetyloxy-3-methylpent-2-enoyl)amino]propanoic acid | present | LOTUS | |
| 3-Deoxyaureosurfactin | present | LOTUS | |
| Antibiotic R 106IIa | present | LOTUS | |
| Aureobasidin E | present | LOTUS | |
| Aureobasidin I | present | LOTUS | |
| Aureobasidin S1 | present | LOTUS | |
| aureobasidin S2a | present | LOTUS |
A DNA barcode is a short, standardised stretch of genes that works like a fingerprint — enough to tell one species from another. Below is the molecular trace Aureobasidium pullulans has left across the world's sequence archives.
At a glance
★ the standard DNA barcode for this group — the short region actually read to tell this species apart. The rest are extra genes sequenced along the way.
The complete instruction manual Aureobasidium pullulans carries — its genome. We read it from three angles — how big it is, how the DNA is packed into chromosomes, and how completely it has been sequenced — and explain how to read each value as you go.
Genome sizehow big the whole instruction manual is
Measured in base pairs (bp) — the individual letters of DNA (human ≈ 3.2 Gb, a bacterium a few million). The chart places this genome on a logarithmic scale — each step to the right is ten times bigger — among reference organisms. Across species a bigger genome loosely tracks with larger cells, slower growth and lower-energy lifestyles (powered flight favours small genomes) — yet it does not imply more genes or a more advanced organism (the long-standing C-value paradox).
Sequencing statusassembly quality — how far to trust these numbers
Assembly level tells you how finished the sequence is — from fragmented contigs, through scaffolds, up to a full chromosome-level assembly. BUSCO % estimates completeness: the share of genes expected to be present that were actually found. These describe the data quality, not the organism.
Record type1 723 records
Range
Depth
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Museum / Voucheredphysical evidence
Backed by a physical specimen — a herbarium sheet, sample or voucher held in a collection. “Vouchered” means supported by material evidence, not just an observation.
Cultivated / Captivenot free-living
A living individual in a botanical garden, zoo or nursery — cultivated or kept, not free-living.
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Holding institutions9 of 29 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
| Institution | Specimens |
|---|---|
| University of Athens, Hellenic Collection of Pathogenic Fungilocation not on record | 11 |
| Universidad Nacional de Colombialocation not on record | 9 |
| Pullman, US | 6 |
| Annamalai University, Faculty of Marine Scienceslocation not on record | 6 |
| BASElocation not on record | 6 |
| Slovenian Forestry Institutelocation not on record | 6 |
| Southeastern Louisiana University, Vertebrate Museumlocation not on record | 4 |
| Bernard Price Institute for Palaeontological Researchlocation not on record | 3 |
| ILLSlocation not on record | 3 |
| TNMlocation not on record | 3 |
| Institut Pasteur, Parislocation not on record | 3 |
| Philadelphia, US | 3 |
| Sydney Medical Schoollocation not on record | 3 |
| San Sebastián, ES | 3 |
| UFPElocation not on record | 3 |
| Catholic University of Pekinglocation not on record | 2 |
| DPIlocation not on record | 2 |
| Auckland, NZ | 2 |
| University of Uppsalalocation not on record | 2 |
| Bronx, US | 2 |
| National Institute of Biological Resourceslocation not on record | 2 |
| California State University, East Baylocation not on record | 1 |
| Swiss Federal Research Institute WSLlocation not on record | 1 |
| Uppsala, SE | 1 |
| Museo Entomologico de Leonlocation not on record | 1 |
| Academy of Sciences of the Republic of Uzbekistanlocation not on record | 1 |
| Odawara, JP | 1 |
| CA | 1 |
| Tartu, EE | 1 |
Cultivated / Captivenot free-living
A living individual in a botanical garden, zoo or nursery — cultivated or kept, not free-living.
Where the DNA of Aureobasidium pullulans was picked up in samples of water, soil or air — nobody saw the organism, only its DNA left behind. A trace is a clue that the species was near, not a confirmed sighting.
Signal
Where its DNA was found
How strong is each trace?
Measured at samplingin-field
Modelled climatemodelled
How to read this: each dot is one detection of this species' DNA in an environmental sample. The confidence meter weighs how many independent studies and places back up the signal — one detection in one study is a hint; many across several studies is solid. Records dated before 2008 (when eDNA methods began) are treated as likely mislabeled and left off the map.