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. 1971 Mar;105(3):690–700. doi: 10.1128/jb.105.3.690-700.1971

Comparative Physiological Studies of the Yeast and Mycelial Forms of Histoplasma capsulatum: Uptake and Incorporation of l-Leucine

Rishab K Gupta a,1, Dexter H Howard a
PMCID: PMC248488  PMID: 4323295

Abstract

l-Leucine entered the cells of both morphological forms of Histoplasma capsulatum by a permease-like system at low external concentrations of substrate. However, at levels greater than 5 × 10−5m l-leucine, the amino acid entered the cells both through a simple diffusion-like process and the permease-like system. The rate of the amino acid diffusion into yeast and mycelial forms appeared to be the same, whereas the initial rate of accumulation through the permease-like system was 5 to 10 times faster in the mycelial phase than it was in the yeast phase. The Michaelis constants were 2.2 × 10−5m in yeast phase and 2 × 10−5m in mycelial phase cells. Transport of l-leucine at an external concentration of 10−5m showed all of the characteristics of a system of active transport, which was dependent on temperature and pH. Displacement or removal of the α-amino group, or modification of the α-carboxyl group abolished amino acid uptake. The process was competitively inhibited by neutral aliphatic side-chain amino acids (inhibition constants ranged from 1.5 × 10−5 to 6.2 × 10−5m). Neutral aromatic side-chain amino acids and the d-isomers of leucine and valine did not inhibit l-leucine uptake. These data were interpreted to mean that the l-leucine transport system is stereospecific and is highly specific for neutral aliphatic side-chain amino acids. Incorporation of l-leucine into macromolecules occurred at almost the same rate in both morphological forms of the fungus. The mycelial phase but not the yeast phase showed a slight initial lag in incorporation. In both morphological forms the intracellular pool of l-leucine was of limited capacity, and the total uptake of the amino acid was a function of intracellular pool size. The initial rate of l-leucine uptake was independent of the level of intracellular pool. Both morphological forms deaminated and degraded only a minor fraction of the accumulated leucine.

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Selected References

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  1. AMES G. F. UPTAKE OF AMINO ACIDS BY SALMONELLA TYPHIMURIUM. Arch Biochem Biophys. 1964 Jan;104:1–18. doi: 10.1016/s0003-9861(64)80028-x. [DOI] [PubMed] [Google Scholar]
  2. BUTTIN G., COHEN G. N., MONOD J., RICKENBERG H. V. La galactoside-perméase d'Escherichia coli. Ann Inst Pasteur (Paris) 1956 Dec;91(6):829–857. [PubMed] [Google Scholar]
  3. DANCIS J., HUTZLER J., LEVITZ M. THIN-LAYER CHROMATOGRAPHY AND SPECTROPHOTOMETRY OF ALPHA-KETOACID HYDRAZONES. Biochim Biophys Acta. 1963 Oct 8;78:85–90. doi: 10.1016/0006-3002(63)91612-3. [DOI] [PubMed] [Google Scholar]
  4. Gale E. F., Folkes J. P. The effect of lipids on the accumulation of certain amino acids by Staphylococcus aureus. Biochim Biophys Acta. 1967 Oct 2;144(2):461–466. doi: 10.1016/0005-2760(67)90177-4. [DOI] [PubMed] [Google Scholar]
  5. Gilbert B. E., Howard D. H. Uptake of Cystine by the Yeast Phase of Histoplasma capsulatum. Infect Immun. 1970 Aug;2(2):139–144. doi: 10.1128/iai.2.2.139-144.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Grenson M. Multiplicity of the amino acid permeases in Saccharomyces cerevisiae. II. Evidence for a specific lysine-transporting system. Biochim Biophys Acta. 1966 Oct 31;127(2):339–346. doi: 10.1016/0304-4165(66)90388-6. [DOI] [PubMed] [Google Scholar]
  7. HANKS J. H., WALLACE J. H. Determination of cell viability. Proc Soc Exp Biol Med. 1958 May;98(1):188–192. doi: 10.3181/00379727-98-23985. [DOI] [PubMed] [Google Scholar]
  8. Halpern Y. S., Even-Shoshan A. Properties of the glutamate transport system in Escherichia coli. J Bacteriol. 1967 Mar;93(3):1009–1016. doi: 10.1128/jb.93.3.1009-1016.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. KEMPNER E. S., COWIE D. B. Metabolic pools and the utilization of amino acid analogs for protein synthesis. Biochim Biophys Acta. 1960 Aug 26;42:401–408. doi: 10.1016/0006-3002(60)90817-9. [DOI] [PubMed] [Google Scholar]
  10. Kay W. W., Gronlund A. F. Amino acid pool formation in Pseudomonas aeruginosa. J Bacteriol. 1969 Jan;97(1):282–291. doi: 10.1128/jb.97.1.282-291.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kay W. W., Gronlund A. F. Proline transport by Pseudomonas aeruginosa. Biochim Biophys Acta. 1969;193(2):444–455. doi: 10.1016/0005-2736(69)90203-x. [DOI] [PubMed] [Google Scholar]
  12. Krulwich T. A., Ensign J. C. Alteration of glucose metabolism of Arthrobacter crystallopoietes by compounds which induce sphere to rod morphogenesis. J Bacteriol. 1969 Feb;97(2):526–534. doi: 10.1128/jb.97.2.526-534.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Pavlasova E., Harold F. M. Energy coupling in the transport of beta-galactosides by Escherichia coli: effect of proton conductors. J Bacteriol. 1969 Apr;98(1):198–204. doi: 10.1128/jb.98.1.198-204.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. 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]
  15. Slayman C. W., Tatum E. L. Potassium transport in Neurospora. 3. Isolation of a transport mutant. Biochim Biophys Acta. 1965 Sep 27;109(1):184–193. doi: 10.1016/0926-6585(65)90102-0. [DOI] [PubMed] [Google Scholar]
  16. WILLIAMSON D. H., SCOPES A. W. The behaviour of nucleic acids in synchronously dividing cultures of Saccharomyces cerevisiae. Exp Cell Res. 1960 Aug;20:338–349. doi: 10.1016/0014-4827(60)90162-2. [DOI] [PubMed] [Google Scholar]
  17. Wiley W. R., Matchett W. H. Tryptophan transport in Neurospora crassa. I. Specificity and kinetics. J Bacteriol. 1966 Dec;92(6):1698–1705. doi: 10.1128/jb.92.6.1698-1705.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Yabu K. Amino acid transport in Mycobacterium smegmatis. J Bacteriol. 1970 Apr;102(1):6–13. doi: 10.1128/jb.102.1.6-13.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]

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