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. 1980 Jan;141(1):10–19. doi: 10.1128/jb.141.1.10-19.1980

Relationship Between Cell Size and Efficiency of Synchronization During Nitrogen-Limited Phased Cultivation of Candida utilis

K Chandapillai Thomas 1, Peter S S Dawson 1, Brian L Gamborg 1, Lee Steinhuer 1
PMCID: PMC293520  PMID: 7188767

Abstract

Under the phased method of cultivation the yeast Candida utilis grew and divided synchronously. The newly formed cells were relatively small, and a new cell cycle was not initiated until the cells could attain a certain minimum size (critical size). Although the cells expanded to some extent after division, the critical size was not reached until a fresh supply of medium was provided. With the arrival of the fresh supply of growth medium at the beginning of the phasing period, the cells expanded rapidly, and new cell cycles were initiated. The cells continued to expand until the growth-limiting nutrient (nitrogen source) was exhausted or until 90 min, which ever occurred first. Usually, buds emerged at a constant time after the start of the phasing period. The time of bud emergence was independent of the size attained by the cells during the expansion phase of growth. The results indicated that it was initiation of the cell cycle that was under size control, and not bud emergence. Bud emergence seemed to be under the control of a timer. The start of this timer seemed to be at or immediately after the beginning of the phasing period. Protein synthesis was essential for the initiation and expansion of buds. However, inhibition of protein synthesis by cycloheximide did not prevent unbudded cells or the parent portion of budded cells from expanding. Cycloheximide seemed to abolish the control mechanism(s) which prevented the cells from expanding after they had reached the maximum size.

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Selected References

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

  1. Barford J. P., Hall R. J. Estimation of the length of cell cycle phases from asynchronous cultures of Saccharomyces cerevisiae. Exp Cell Res. 1976 Oct 15;102(2):276–284. doi: 10.1016/0014-4827(76)90043-4. [DOI] [PubMed] [Google Scholar]
  2. Bridger W. A., Paranchych W. relA Gene control of bacterial glycogen synthesis. Can J Biochem. 1978 Jun;56(6):403–406. doi: 10.1139/o78-063. [DOI] [PubMed] [Google Scholar]
  3. Carter B. L., Jagadish M. N. The relationship between cell size and cell division in the yeast Saccharomyces cerevisiae. Exp Cell Res. 1978 Mar 1;112(1):15–24. doi: 10.1016/0014-4827(78)90520-7. [DOI] [PubMed] [Google Scholar]
  4. Dawson P. S. Continuous phased growth, with a modified chemostat. Can J Microbiol. 1965 Dec;11(6):893–903. doi: 10.1139/m65-119. [DOI] [PubMed] [Google Scholar]
  5. Fantes P. A., Nurse P. Control of the timing of cell division in fission yeast. Cell size mutants reveal a second control pathway. Exp Cell Res. 1978 Sep;115(2):317–329. doi: 10.1016/0014-4827(78)90286-0. [DOI] [PubMed] [Google Scholar]
  6. Fantes P., Nurse P. Control of cell size at division in fission yeast by a growth-modulated size control over nuclear division. Exp Cell Res. 1977 Jul;107(2):377–386. doi: 10.1016/0014-4827(77)90359-7. [DOI] [PubMed] [Google Scholar]
  7. Hartwell L. H. Cell division from a genetic perspective. J Cell Biol. 1978 Jun;77(3):627–637. doi: 10.1083/jcb.77.3.627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hartwell L. H., Culotti J., Pringle J. R., Reid B. J. Genetic control of the cell division cycle in yeast. Science. 1974 Jan 11;183(4120):46–51. doi: 10.1126/science.183.4120.46. [DOI] [PubMed] [Google Scholar]
  9. Hartwell L. H., Unger M. W. Unequal division in Saccharomyces cerevisiae and its implications for the control of cell division. J Cell Biol. 1977 Nov;75(2 Pt 1):422–435. doi: 10.1083/jcb.75.2.422. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ishiguro E. E., Ramey W. D. Effect of amino acid deprivation and chloramphenicol treatment on cell sizes of rel+ and relA- strains of Escherichia coli. Can J Microbiol. 1978 Jun;24(6):761–764. doi: 10.1139/m78-127. [DOI] [PubMed] [Google Scholar]
  11. Jacobson G. K., Parks L. W. Cell division and deoxyribonucleic acid synthesis after a nutritional shift-up of Saccharomyces cerevisiae. J Bacteriol. 1973 May;114(2):876–877. doi: 10.1128/jb.114.2.876-877.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jagadish M. N., Carter B. L. Genetic control of cell division in yeast cultured at different growth rates. Nature. 1977 Sep 8;269(5624):145–147. doi: 10.1038/269145a0. [DOI] [PubMed] [Google Scholar]
  13. Johnston G. C. Cell size and budding during starvation of the yeast Saccharomyces cerevisiae. J Bacteriol. 1977 Nov;132(2):738–739. doi: 10.1128/jb.132.2.738-739.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Johnston G. C., Ehrhardt C. W., Lorincz A., Carter B. L. Regulation of cell size in the yeast Saccharomyces cerevisiae. J Bacteriol. 1979 Jan;137(1):1–5. doi: 10.1128/jb.137.1.1-5.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Johnston G. C., Pringle J. R., Hartwell L. H. Coordination of growth with cell division in the yeast Saccharomyces cerevisiae. Exp Cell Res. 1977 Mar 1;105(1):79–98. doi: 10.1016/0014-4827(77)90154-9. [DOI] [PubMed] [Google Scholar]
  16. Johnston G. C., Singer R. A., McFarlane S. Growth and cell division during nitrogen starvation of the yeast Saccharomyces cerevisiae. J Bacteriol. 1977 Nov;132(2):723–730. doi: 10.1128/jb.132.2.723-730.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Müller J., Dawson P. S. The operational flexibility of the phased culture technique, as observed by changes in the cell cycle of Candida utilis. Can J Microbiol. 1968 Oct;14(10):1115–1126. doi: 10.1139/m68-187. [DOI] [PubMed] [Google Scholar]
  18. Nurse P. Genetic control of cell size at cell division in yeast. Nature. 1975 Aug 14;256(5518):547–551. doi: 10.1038/256547a0. [DOI] [PubMed] [Google Scholar]
  19. Slater M. L., Sharrow S. O., Gart J. J. Cell cycle of Saccharomycescerevisiae in populations growing at different rates. Proc Natl Acad Sci U S A. 1977 Sep;74(9):3850–3854. doi: 10.1073/pnas.74.9.3850. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Sumrada R., Cooper T. G. Control of vacuole permeability and protein degradation by the cell cycle arrest signal in Saccharomyces cerevisiae. J Bacteriol. 1978 Oct;136(1):234–246. doi: 10.1128/jb.136.1.234-246.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Thomas K. C., Dawson P. S., Gamborg B. L. Differential growth rates of Candida utilis mother and daughter cells under phased cultivation. J Bacteriol. 1980 Jan;141(1):1–9. doi: 10.1128/jb.141.1.1-9.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Thomas K. C., Dawson P. S. Variations in the adenylate energy charge during phased growth (cell cycle) of Candida utilis under energy excess and energy-limiting growth conditions. J Bacteriol. 1977 Oct;132(1):36–43. doi: 10.1128/jb.132.1.36-43.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]

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