Regulation of Amino Acid Transport in Saccharomyces cerevisiae

Frans Bianchi, Joury S Van't Klooster, Stephanie J Ruiz, Bert Poolman*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

8 Citations (Scopus)

Abstract

SUMMARYWe review the mechanisms responsible for amino acid homeostasis in Saccharomyces cerevisiae and other fungi. Amino acid homeostasis is essential for cell growth and survival. Hence, the de novo synthesis reactions, metabolic conversions, and transport of amino acids are tightly regulated. Regulation varies from nitrogen pool sensing to control by individual amino acids and takes place at the gene (transcription), protein (posttranslational modification and allostery), and vesicle (trafficking and endocytosis) levels. The pools of amino acids are controlled via import, export, and compartmentalization. In yeast, the majority of the amino acid transporters belong to the APC (amino acid-polyamine-organocation) superfamily, and the proteins couple the uphill transport of amino acids to the electrochemical proton gradient. Although high-resolution structures of yeast amino acid transporters are not available, homology models have been successfully exploited to determine and engineer the catalytic and regulatory functions of the proteins. This has led to a further understanding of the underlying mechanisms of amino acid sensing and subsequent downregulation of transport. Advances in optical microscopy have revealed a new level of regulation of yeast amino acid transporters, which involves membrane domain partitioning. The significance and the interrelationships of the latest discoveries on amino acid homeostasis are put in context.

Original languageEnglish
Article numbere00024-19
JournalMicrobiology and Molecular Biology Reviews
Volume83
Issue number4
DOIs
Publication statusPublished - 20-Nov-2019

Keywords

  • MAJOR FACILITATOR SUPERFAMILY
  • VACUOLAR-MEMBRANE-VESICLES
  • YEAST PLASMA-MEMBRANE
  • DETERGENT-RESISTANT MEMBRANES
  • MITOCHONDRIAL ADP/ATP CARRIER
  • GAMMA-AMINOBUTYRIC-ACID
  • KINASE-A PATHWAY
  • HIGH-AFFINITY
  • UBIQUITIN-LIGASE
  • STRUCTURAL BASIS

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