1975
DOI: 10.1080/00362177585190261
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Amino acid synthetic media for fungal pathogens based on aminopeptidase specificities:Histoplasma capsulatum, Blastomyces dermititidis, Paracoccidioides brasiliensis and Cryptococcus neoformans.

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Cited by 19 publications
(6 citation statements)
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“…The haploid strains W303 and its rad52 derivative (LSY1029-13B), both ADE2 RAD5, were kindly provided by Lorraine Symington, from Columbia University. To inspect for hyphal growth stationary phase cultures were inoculated on agar plates with SPIDER medium, M199 medium, pH 7,9 (Gifco BRL, Life technologies), or Leé s medium (Lee et al, 1975;Liu et al, 1994), prepared as described before (Andaluz et al, 2006). Colonies were visualized with the naked eye and then microscopically inspected.…”
Section: Strains and Culture Mediamentioning
confidence: 99%
“…The haploid strains W303 and its rad52 derivative (LSY1029-13B), both ADE2 RAD5, were kindly provided by Lorraine Symington, from Columbia University. To inspect for hyphal growth stationary phase cultures were inoculated on agar plates with SPIDER medium, M199 medium, pH 7,9 (Gifco BRL, Life technologies), or Leé s medium (Lee et al, 1975;Liu et al, 1994), prepared as described before (Andaluz et al, 2006). Colonies were visualized with the naked eye and then microscopically inspected.…”
Section: Strains and Culture Mediamentioning
confidence: 99%
“…These parasites survive best where the combination of their own and host aminopeptidases produces an adequate supply of necessary amino acids. Lee et al (9,10) clearly related the substrate specificities of Candida albicans, Histoplasma capsulatum, Blastomyces dermatitidis, Paracoccidioides brasiliensis, and Cryptococcus neoformans to their amino acid growth requirements. Aminopeptidase profiles identified the N-terminal amino acids most rapidly liberated by these organisms.…”
Section: Discussionmentioning
confidence: 99%
“…A loopful of cells from the culture plate of each strain was transferred to a chemically defined synthetic liquid medium (9,10), and the cells were allowed to grow overnight at 25°C for C. albicans and at 37°C for all other yeasts on a gyratory shaker at 200 rpm. An aliquot of these cultures was then added to fresh liquid medium, and the cultures were allowed to grow under the conditions described above.…”
Section: Methodsmentioning
confidence: 99%