Proteomic and functional characterization of a Chlamydomonas reinhardtii mutant lacking the mitochondrial alternative oxidase 1

J Proteome Res. 2010 Jun 4;9(6):2825-38. doi: 10.1021/pr900866e.

Abstract

In the present work, we have isolated by RNA interference and characterized at the functional and the proteomic levels a Chlamydomonas reinhardtii strain devoid of the mitochondrial alternative oxidase 1 (AOX1). The AOX1-deficient strain displays a remarkable doubling of the cell volume and biomass without alteration of the generation time or change in total respiratory rate, with a significantly higher ROS production. To identify the molecular adaptation underlying these observations, we have carried out a comparative study of both the mitochondrial and the cellular soluble proteomes. Our results indicate a strong up-regulation of the ROS scavenging systems and important quantitative modifications of proteins involved in the primary metabolism, namely an increase of enzymes involved in anabolic pathways and a concomitant general down-regulation of enzymes of the main catabolic pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Chlamydomonas reinhardtii / genetics
  • Chlamydomonas reinhardtii / metabolism*
  • Electrophoresis, Gel, Two-Dimensional
  • Gene Silencing / physiology*
  • Hydrogen Peroxide / metabolism
  • Mitochondrial Proteins / metabolism
  • Mutation
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism
  • Oxidoreductases / physiology*
  • Photosynthesis
  • Plant Proteins
  • Proteins / metabolism
  • Proteome / metabolism*
  • Proteomics
  • Signal Transduction
  • Subcellular Fractions / metabolism

Substances

  • Mitochondrial Proteins
  • Plant Proteins
  • Proteins
  • Proteome
  • Hydrogen Peroxide
  • Oxidoreductases
  • alternative oxidase