Literature DB >> 1679011

Vector-mediated overexpression of catalase A in the yeast Saccharomyces cerevisiae induces inclusion body formation.

M Binder1, M Schanz, A Hartig.   

Abstract

To study the morphological effects of overexpression of catalase A in yeast, the gene coding for catalase A was introduced into Saccharomyces cerevisiae on a multicopy vector. After induction of microbody biogenesis and catalase A expression by growth on oleic acid as sole carbon source, cells were analyzed by immunofluorescence and immunoelectron microscopy. In addition, overexpression of catalase A was studied by quantitative immunoblotting and by activity measurement. Quantitative immunoblotting resulted in a 16-fold difference between immunoreactive material from transformed and non-transformed cells. An 18-fold increase of enzyme activity was measured in transformed cells due to overexpression of catalase A from plasmid pAH521. Immunofluorescent staining of semithin sections of Lowicryl HM20-embedded cells with anti-catalase localized peroxisomes and--at a low percentage--larger particles. By immunoelectron microscopy, these larger structures could be identified as agranular, electron-dense aggregates which are morphologically clearly distinct from the cytoplasm and not bounded by a membrane. These structures, which have been named inclusion bodies, contain catalase A but not other peroxisomal enzymes like thiolase. These findings suggest that cells are capable of compensating for overproduced proteins by formation of particular types of structures.

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Year:  1991        PMID: 1679011

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  8 in total

1.  Crystallization and preliminary structural analysis of catalase A from Saccharomyces cerevisiae.

Authors:  S Berthet; L M Nykyri; J Bravo; M J Mate; C Berthet-Colominas; P M Alzari; F Koller; I Fita
Journal:  Protein Sci       Date:  1997-02       Impact factor: 6.725

Review 2.  Immunogold labeling of yeast cells: an efficient tool for the study of protein targeting and morphological alterations due to overexpression and inactivation of genes.

Authors:  M Binder; A Hartig; T Sata
Journal:  Histochem Cell Biol       Date:  1996-07       Impact factor: 4.304

3.  Homogenates of yeast cultures with engineered catalases F148V and V111A reveal higher specific activities after incubation at permissive temperature.

Authors:  M Zámocký; F Koller
Journal:  Folia Microbiol (Praha)       Date:  1997       Impact factor: 2.099

4.  Giant yeast cells with nonrecyclable ribonucleotide reductase.

Authors:  Emilie Ma; Arach Goldar; Jean-Marc Verbavatz; Marie-Claude Marsolier-Kergoat
Journal:  Mol Genet Genomics       Date:  2011-03-27       Impact factor: 3.291

Review 5.  Recombinant protein production in yeasts.

Authors:  Danilo Porro; Michael Sauer; Paola Branduardi; Diethard Mattanovich
Journal:  Mol Biotechnol       Date:  2005-11       Impact factor: 2.695

6.  A striking quality control subcompartment in Saccharomyces cerevisiae: the endoplasmic reticulum-associated compartment.

Authors:  Gregory Huyer; Gaby L Longsworth; Deborah L Mason; Monica P Mallampalli; J Michael McCaffery; Robin L Wright; Susan Michaelis
Journal:  Mol Biol Cell       Date:  2003-12-10       Impact factor: 4.138

7.  Two independent peroxisomal targeting signals in catalase A of Saccharomyces cerevisiae.

Authors:  F Kragler; A Langeder; J Raupachova; M Binder; A Hartig
Journal:  J Cell Biol       Date:  1993-02       Impact factor: 10.539

8.  Functional inclusion bodies produced in the yeast Pichia pastoris.

Authors:  Fabián Rueda; Brigitte Gasser; Alejandro Sánchez-Chardi; Mònica Roldán; Sandra Villegas; Verena Puxbaum; Neus Ferrer-Miralles; Ugutz Unzueta; Esther Vázquez; Elena Garcia-Fruitós; Diethard Mattanovich; Antonio Villaverde
Journal:  Microb Cell Fact       Date:  2016-10-01       Impact factor: 5.328

  8 in total

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