Distinguishing phosphatidic acid pools from de novo synthesis, PLD, and DGK

Methods Mol Biol. 2013:1009:55-62. doi: 10.1007/978-1-62703-401-2_6.

Abstract

In plants, phosphatidic acid (PA) functions as a metabolic precursor in the biosynthesis of glycerolipids, but it also acts as a key signaling lipid in the response to environmental stress conditions (Testerink and Munnik, J Exp Bot 62:2349-2361, 2011). In vivo (32)P-radiolabeling assays have shown the level of PA to increase within seconds/minutes of exposure to a stimulus. This response can be due to the activity of diacylglycerol kinase (DGK) and/or phospholipase D (PLD). A method is described to investigate which of the pathways is responsible for PA accumulation under a particular stress condition. First, a differential (32)P-radiolabeling protocol is used to discriminate (32)P-PA pools that are rapidly labeled versus those requiring long prelabeling times, reflecting DGK and PLD activities, respectively. Second, to specifically monitor the contribution of PLD, a transphosphatidylation assay is applied, which makes use of the artificial lipid phosphatidylbutanol as an in vivo marker of PLD activity.

MeSH terms

  • Diacylglycerol Kinase / metabolism*
  • Isotope Labeling
  • Phosphatidic Acids / metabolism*
  • Phospholipase D / metabolism*
  • Phosphorus Radioisotopes
  • Time Factors

Substances

  • Phosphatidic Acids
  • Phosphorus Radioisotopes
  • Diacylglycerol Kinase
  • Phospholipase D