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. 1978 Sep;135(3):987–992. doi: 10.1128/jb.135.3.987-992.1978

Cystine reductase in the dimorphic fungus Histoplasma capsulatum.

B Maresca, E Jacobson, G Medoff, G Kobayashi
PMCID: PMC222474  PMID: 211119

Abstract

Organo-sulfur compounds favor the transition of mycelia of Histoplasma capsulatum to the yeast form (6, 8). Investigation of the role of cystine in the transition revealed that the two phases concentrated this amino acid at comparable rates and that mutants defective in the uptake of cystine were still able to undergo the transition normally. Uptake of cystine is therefore probably not a requirement for transition to or maintenance of the yeast phase. Both phases contained a reduced nicotinamide adenine dinucleotide phosphate-dependent glutathione reductase; but a reduced nicotinamide adenine dinucleotide-dependent cystine reductase was detectable only in the yeast phase. The cystine reductase appeared early in the transition of mycelium to yeast. Treatment of mycelia with p-chloromercuriphenylsulfonic acid, which prevented the transition to yeast, had no effect on cystine uptake but strongly inhibited the cystine reductase. These results suggest that cystine reductase may provide reduced sulfhydryl groups involved in the transition of mycelium to yeast.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Cheung S. C., Kobayashi G. S., Medoff G. Antibiotic sensitivity of the yeast and mycelial phases of Histoplasma capsulatum. Sabouraudia. 1976 Mar;14(1):99–103. doi: 10.1080/00362177685190151. [DOI] [PubMed] [Google Scholar]
  2. Cheung S. C., Medoff G., Schlessinger D., Kobayashi G. S. Response of yeast and mycelial phases of Histoplasma capsulatum to amphotericin B and actinomycin D. Antimicrob Agents Chemother. 1975 Oct;8(4):498–503. doi: 10.1128/aac.8.4.498. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Conant N. F. Cultural Study of the Life-Cycle of Histoplasma capsulatum Darling 1906. J Bacteriol. 1941 May;41(5):563–579. doi: 10.1128/jb.41.5.563-579.1941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  5. Maresca B., Medoff G., Schlessinger D., Kobayashi G. S. Regulation of dimorphism in the pathogenic fungus Histoplasma capsulatum. Nature. 1977 Mar 31;266(5601):447–448. doi: 10.1038/266447a0. [DOI] [PubMed] [Google Scholar]
  6. PINE L. Studies on the growth of Histoplasma capsulatum. I. Growth of the yeast phase in liquid media. J Bacteriol. 1954 Dec;68(6):671–679. doi: 10.1128/jb.68.6.671-679.1954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Rippon J. W. Monitored environment system to control cell growth, morphology, and metabolic rate in fungi by oxidation-reduction potentials. Appl Microbiol. 1968 Jan;16(1):114–121. doi: 10.1128/am.16.1.114-121.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. SALVIN S. B. Growth of the yeastlike phase of Histoplasma capsulatum in a fluid medium. J Bacteriol. 1950 Feb;59(2):312–313. doi: 10.1128/jb.59.2.312-313.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. SCHERR G. H. Studies on the dimorphism of Histoplasma capsulatum. I. The roles of -SH groups and incubation temperature. Exp Cell Res. 1957 Feb;12(1):92–107. doi: 10.1016/0014-4827(57)90296-3. [DOI] [PubMed] [Google Scholar]

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