Literature DB >> 1093169

The relationship between enzyme activity, cell geometry, and fitness in Saccharomyces cerevisiae.

R L Weiss, J R Kukora, J Adams.   

Abstract

The relationship between enzyme activity, cell geometry, and the ploidy levels has been investigated in Saccharomyces cerevisiae. Diploid cells have 1.57 times the volume of haploid cells under nonlimiting growth conditions (minimal medium). However, when diploid cells are grown under conditions of carbon limitation, they have the same volume as haploid cells. Thus, by altering the environmental conditions, cell size can be varied independently of the degree of ploidy. The results indicate that the basic biochemical parameters of the cell are primarily determined by cell geometry rather than ploidy level. RNA content, protein content, and ornithine transcarbamylase (carbamoylphosphate: L-ornithine carbamoyltransferase, EC 2.1.3.3), tryptophan synthetase [L-serine hydro-lyase (adding indole), EC 4.2.1.20], and invertase (alpha-D-glucoside glucohydrolase, Ec 3.2.1.20) activity are related to cell volume, whereas acid phosphatase (orthophosphoric-monoester phosphohydrolase, EC 3.1.3.2) activity, a cell surface enzyme, is related to the surface area of the cells. Fitness is determined by the activity of certain cell surface enzymes, such as acid phosphatase, diploids would be expected to have a lower fitness than haploids because of the lower surface area/volume ratio. However, when fitness is determined by the activity of an internal enzyme, diploids would be expected to have the same fitness as haploids. Results from competition experiments between haploids and diploids are consistent with these predictions. The significance of these results to the evolution of diploidy as the predominant phase of the life cycle of higher plants and animals is discussed.

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Year:  1975        PMID: 1093169      PMCID: PMC432406          DOI: 10.1073/pnas.72.3.794

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  22 in total

1.  GENE DOSAGE AND GALACTOSE UTILIZATION BY SACCHAROMYCES TETRAPLOIDS.

Authors:  N M NELSON; H C DOUGLAS
Journal:  Genetics       Date:  1963-12       Impact factor: 4.562

2.  Studies on the mechanism of the tryptophan synthetase reaction.

Authors:  J A DEMOSS
Journal:  Biochim Biophys Acta       Date:  1962-08-13

3.  Radiobiological and genetic studies on a polyploid series (haploid to hexaploid) of Saccharomyces cerevisiae.

Authors:  R K MORTIMER
Journal:  Radiat Res       Date:  1958-09       Impact factor: 2.841

4.  The nucleic acids in a polyploid series of Saccharomyces.

Authors:  M OGUR; S MINCKLER; G LINDEGREN; C C LINDEGREN
Journal:  Arch Biochem Biophys       Date:  1952-09       Impact factor: 4.013

5.  Studies on the kinetics of the enzyme sequence mediating arginine synthesis in Saccharomyces cerevisiae.

Authors:  F Hilger; M Culot; M Minet; A Pierard; M Grenson; J M Wiame
Journal:  J Gen Microbiol       Date:  1973-03

6.  Intracellular localization of ornithine and arginine pools in Neurospora.

Authors:  R L Weiss
Journal:  J Biol Chem       Date:  1973-08-10       Impact factor: 5.157

7.  External enzymes of yeast: their nature and formation.

Authors:  J O Lampen
Journal:  Antonie Van Leeuwenhoek       Date:  1968       Impact factor: 2.271

8.  Effect of gene dosage on tryptophan synthetase activity in Saccharomyces cerevisiae.

Authors:  O Ciferri; S Sora; O Tiboni
Journal:  Genetics       Date:  1969-03       Impact factor: 4.562

9.  Evidence for chain termination by super-suppressible mutants in yeast.

Authors:  T R Manney
Journal:  Genetics       Date:  1968-12       Impact factor: 4.562

10.  Beta-fructofuranosidase from grape berries.

Authors:  W N Arnold
Journal:  Biochim Biophys Acta       Date:  1965-10-25
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  27 in total

Review 1.  Ploidy Variation in Fungi: Polyploidy, Aneuploidy, and Genome Evolution.

Authors:  Robert T Todd; Anja Forche; Anna Selmecki
Journal:  Microbiol Spectr       Date:  2017-07

2.  Mutational effects depend on ploidy level: all else is not equal.

Authors:  Aleeza C Gerstein
Journal:  Biol Lett       Date:  2012-10-10       Impact factor: 3.703

3.  Assessment of cellular mechanisms contributing to cAMP compartmentalization in pulmonary microvascular endothelial cells.

Authors:  Wei P Feinstein; Bing Zhu; Silas J Leavesley; Sarah L Sayner; Thomas C Rich
Journal:  Am J Physiol Cell Physiol       Date:  2011-11-23       Impact factor: 4.249

4.  Why it pays for bacteria to delete disused DNA and to maintain megaplasmids.

Authors:  A H Stouthamer; S A Kooijman
Journal:  Antonie Van Leeuwenhoek       Date:  1993-01       Impact factor: 2.271

5.  Free tryptophan pool and tryptophan biosynthetic enzymes in Saccharomyces cerevisiae.

Authors:  P A Fantes; L M Roberts; R Huetter
Journal:  Arch Microbiol       Date:  1976-03-19       Impact factor: 2.552

Review 6.  Selection in chemostats.

Authors:  D E Dykhuizen; D L Hartl
Journal:  Microbiol Rev       Date:  1983-06

7.  Structure of evolving populations of Saccharomyces cerevisiae: adaptive changes are frequently associated with sequence alterations involving mobile elements belonging to the Ty family.

Authors:  J Adams; P W Oeller
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

8.  Tryptophan biosynthesis in Saccharomyces cerevisiae: control of the flux through the pathway.

Authors:  G Miozzari; P Niederberger; R Hütter
Journal:  J Bacteriol       Date:  1978-04       Impact factor: 3.490

9.  Effect of carbon source on enzymes and metabolites of arginine metabolism in Neurospora.

Authors:  C Drainas; R L Weiss
Journal:  J Bacteriol       Date:  1980-01       Impact factor: 3.490

10.  Regulation of release factor expression using a translational negative feedback loop: a systems analysis.

Authors:  Russell Betney; Eric de Silva; Christina Mertens; Yvonne Knox; J Krishnan; Ian Stansfield
Journal:  RNA       Date:  2012-10-25       Impact factor: 4.942

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