Initial proteome analysis of caffeine-induced proteins in Aspergillus tamarii using two-dimensional fluorescence difference gel electrophoresis

Appl Biochem Biotechnol. 2012 Apr;166(8):2064-77. doi: 10.1007/s12010-012-9634-7. Epub 2012 Mar 7.

Abstract

Caffeine is toxic to most microorganisms. However, some filamentous fungi, such as Aspergillus tamarii, are able to metabolize this alkaloid when fed caffeine as the sole nitrogen source. The aim of the present work was to identify intracellular A. tamarii proteins, regulated by caffeine, using fluorescence difference two-dimensional gel electrophoresis. Specific proteins from two culture media of A. tamarii grown either on ammonium sulfate or caffeine as the sole nitrogen source were analysed by mass spectrometry. Thirteen out of a total of 85 differentially expressed spots were identified after database search. Identified up-regulated proteins include phosphoglycerate kinase, malate dehydrogenase, dyp-type peroxidase family protein, heat shock protein, Cu, Zn superoxidase dismutase and xanthine dehydrogenase. Some of the proteins identified in this study are involved in the caffeine degradation pathway as well as in stress response, suggesting that stress proteins could be involved in caffeine metabolism in filamentous fungi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspergillus / cytology
  • Aspergillus / drug effects*
  • Aspergillus / metabolism*
  • Caffeine / pharmacology*
  • Down-Regulation / drug effects
  • Fungal Proteins / isolation & purification
  • Fungal Proteins / metabolism*
  • Gene Expression Regulation, Fungal / drug effects
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism
  • Mass Spectrometry
  • Proteomics / methods*
  • Quaternary Ammonium Compounds / pharmacology
  • Spectrometry, Fluorescence
  • Two-Dimensional Difference Gel Electrophoresis / methods*
  • Up-Regulation / drug effects

Substances

  • Fungal Proteins
  • Quaternary Ammonium Compounds
  • Caffeine