Literature DB >> 7023385

Extracellular protein release and its response to pH level in Saccharomyces cerevisiae.

J Weller, B Dorfman, M Soller, A Friedmann.   

Abstract

Saccharomyces cerevisiae grown in batch culture at pH 5.5 releases 0.1 to 0.2 pg protein per cell to the external medium over a period of four to five days, final concentration 20-40 micrograms/ml. Cells grown at pH 3.0 release 10-fold this quantity (1-2 pg/cell, final concentration 100-200 micrograms/ml). A kinetic model based on published behavior of periplasmic protein gave a good fit to the observed kinetics of exoprotein yield. The electrophoretic pattern of exoprotein differed from that of cell lysate protein, and exoprotein synthesis was apparently limited to early stages of the life cycle. These results are consistent with the identification of exoprotein as periplasmic protein released to the external medium through the cell wall. Analysis of the observed kinetics of exoprotein yield, utilizing the kinetic model suggests that the greater exoprotein production of cells grown at pH 3.0 was due entirely to greater synthesis of periplasmic proteins while the fraction of periplasmic protein released per unit time was greater for cells grown at pH 5.5. The latter conclusion is supported by thicker cell walls of cells grown at pH 3.0 as observed by electron microscopy. At an applied level the apparent limitation of exoprotein synthesis to the first few hours of cell life, the slow leakage of exoprotein through the cell wall, and the dilute nature of a yeast suspension do not favor the utilization of yeast cells for direct conversion of substrate into protein released to the external medium.

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Year:  1981        PMID: 7023385     DOI: 10.1007/bf00403391

Source DB:  PubMed          Journal:  Antonie Van Leeuwenhoek        ISSN: 0003-6072            Impact factor:   2.271


  18 in total

1.  Localization of sucrose and maltose fermenting systems in Saccharomyces cerevisiae.

Authors:  D D SUTTON; J O LAMPEN
Journal:  Biochim Biophys Acta       Date:  1962-01-29

2.  The relationship of the cell surface to metabolism. X. The location and function of invertase in the yeast cell.

Authors:  D J DEMIS; A ROTHSTEIN; R MEIER
Journal:  Arch Biochem Biophys       Date:  1954-01       Impact factor: 4.013

3.  A low-viscosity epoxy resin embedding medium for electron microscopy.

Authors:  A R Spurr
Journal:  J Ultrastruct Res       Date:  1969-01

4.  Recovery of exocellular acid phosphatase activity on Saccharomyces mellis after treatment of the organism with reagents that affect the cell surface.

Authors:  R Weimberg
Journal:  J Bacteriol       Date:  1971-12       Impact factor: 3.490

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

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

6.  Thiol induced release of invertase from cell walls of Saccharomyces fragilis.

Authors:  D K Kidby; R Davies
Journal:  Biochim Biophys Acta       Date:  1970-02-24

7.  Invertase and disulphide bridges in the yeast wall.

Authors:  D K Kidby; R Davies
Journal:  J Gen Microbiol       Date:  1970-06

8.  Saccharomyces mutants with invertase formation resistant to repression by hexoses.

Authors:  B S Montenecourt; S C Kuo; J O Lampen
Journal:  J Bacteriol       Date:  1973-04       Impact factor: 3.490

9.  Localization of acid phosphatase in Saccharomyces cerevisiae: a clue to cell wall formation.

Authors:  W A Linnemans; P Boer; P F Elbers
Journal:  J Bacteriol       Date:  1977-08       Impact factor: 3.490

10.  Location of acid phosphatase and -fructofuranosidase within yeast cell envelopes.

Authors:  W N Arnold
Journal:  J Bacteriol       Date:  1972-12       Impact factor: 3.490

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