source w dermatitidis 8656 wild type atcc 34100 hf1 w dermatitidis 8656 ts hyphal form mutant 50 (ATCC)
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Source W Dermatitidis 8656 Wild Type Atcc 34100 Hf1 W Dermatitidis 8656 Ts Hyphal Form Mutant 50, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Article Title: WdStuAp, an APSES Transcription Factor, Is a Regulator of Yeast-Hyphal Transitions in Wangiella ( Exophiala ) dermatitidis
Journal: Eukaryotic Cell
doi: 10.1128/ec.00037-07
Figure Legend Snippet: FIG. 1. Effects of WdSTUA disruption on growth and colony morphology on YPDA at 25°C and 37°C. (A) Yeast cells were spotted (5 l) at 105, 104, 103, and 102 concentrations on YPDA and incubated at 25°C and 37°C. After 4 days, the growth at the spots was photographed without magnification, whereas the surface morphologies at the spots inoculated with the 102 yeast concentration were visualized with a dissecting microscope and also photographed. WT, wild type. (B) Wild-type and Wdstua1A strains cultured with shaking in YPDB at 37°C to late log phase were visualized with a compound light microscope and then photographed. Note that the Wdstua1A strain produced more hyphae that tended to be aggregated. Scale bar, 10 m (applicable to the growth in both photomicrographs).
Techniques Used: Disruption, Incubation, Concentration Assay, Microscopy, Cell Culture, Light Microscopy, Produced
Figure Legend Snippet: FIG. 2. The WdSTUA deletion reduced W. dermatitidis filamentous growth on PDA at 25°C. The wild-type (WT) and Wdstua1A strains were streaked on PDA and incubated at 25°C (A) and 37°C (B). The filamentous growth at the colony edges was visualized with a compound light microscope, and the photomicrographs were taken after 4 days of incubation. Scale bar, 0.2 mm (applicable to all colonies in the figure).
Techniques Used: Incubation, Light Microscopy
Figure Legend Snippet: FIG. 3. The WdSTUA deletion repressed aerial hyphal growth and consequently conidiogenesis. The wild-type (WT) and Wdstua1A strains were inoculated on PDA in slide cultures and incubated at 25°C. Growth at the edge of the medium and protruding into the air space between the slide and coverslip was visualized with a compound light microscope and photographed after 2 weeks of incubation. Scale bar, 10 m (applicable to all the growth in both photomicrographs). The arrow points to a cluster of conidia produced at the terminus of a conidiogenous hypha.
Techniques Used: Incubation, Light Microscopy, Produced
Figure Legend Snippet: FIG. 4. The Wdstua mutant was defective in invasive growth. (A) Wild-type (WT) and Wdstua1A cells were spotted on PDA and incubated at 25°C. After incubation for 8 days, colonies were visualized with a dissecting microscope and photographed. (B) The biomass above the agar was then rinsed away and the remaining, invasive growth photographed again. (C) Cross sections of the growth that invaded the agar. (D) The morphotypes in the invasive growth visualized with a light microscope. Scale bar, 10 m (applicable to the growth in both photomicrographs).
Techniques Used: Mutagenesis, Incubation, Microscopy, Light Microscopy
Figure Legend Snippet: FIG. 5. WdSTUA deletion in the Hf1 strain inhibited filamentous growth on PDA. Wild-type (WT), Wdstua1A, Hf1, and Hf1 Wdstua1 strains were grown on YPDA at 37°C for 6 days (A) and on PDA at 25°C for 6 days (B). The Hf1 and Hf1 Wdstua1 strains were also inoculated on PDA for slide culture at 25°C. After 2 weeks, conidiophores and conidia were visualized with a light microscope and photographed (C). Scale bars, 10 m (applicable to the growth in both photomicrographs). The arrows point to clusters of conidia produced at the termini of conidiogenous hyphae.
Techniques Used: Light Microscopy, Produced
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