Spectrophotometric Assays for Measuring Photorespiratory Glutamate:Glyoxylate and Serine:Glyoxylate Aminotransferase Reactions

Methods Mol Biol. 2024:2792:41-49. doi: 10.1007/978-1-0716-3802-6_4.

Abstract

Glutamate:glyoxylate aminotransferase (GGAT; EC 2.6.1.4) and serine:glyoxylate aminotransferase activities (SGAT; EC 2.6.1.45) are central photorespiratory reactions within plant peroxisomes. Both enzymatic reactions convert glyoxylate, a product of glycolate oxidase, to glycine, a substrate of the mitochondrial glycine decarboxylase complex. The GGAT reaction uses glutamate as an amino group donor and also produces α-ketoglutarate, which is recycled to glutamate in plastids by ferredoxin-dependent glutamate synthase. Using serine, a product of mitochondrial serine hydroxymethyltransferase, as an amino group donor, the SGAT reaction also produces hydroxypyruvate, a substrate of hydroxypyruvate reductase. The activities of these photorespiratory aminotransferases can be measured using indirect, coupled, spectrophotometric assays, detailed herein.

Keywords: Enzyme kinetics; Glutamate:glyoxylate aminotransferase; NADH; Photorespiration; Serine:glyoxylate aminotransferase; Spectrophotometric assay.

MeSH terms

  • Cell Respiration
  • Enzyme Assays / methods
  • Glutamic Acid / metabolism
  • Glyoxylates / metabolism
  • Spectrophotometry* / methods
  • Transaminases* / metabolism

Substances

  • Transaminases
  • glyoxylate aminotransferase
  • Glyoxylates
  • serine-glyoxylate aminotransferase
  • Glutamic Acid