Home > Research > Publications & Outputs > Are Isocitrate Lyase and Phosphoenolpyruvate Ca...
View graph of relations

Are Isocitrate Lyase and Phosphoenolpyruvate Carboxykinase Involved in Gluconeogenesis during Senescence of Barley Leaves and Cucumber Cotyledons?

Research output: Contribution to journalJournal article


  • Zhi-Hui Chen
  • Robert P. Walker
  • Richard M. Acheson
  • László I. Técsi
  • Astrid Wingler
  • Peter John Lea
  • Richard C. Leegood
<mark>Journal publication date</mark>2000
<mark>Journal</mark>Plant and Cell Physiology
Issue number8
Number of pages8
Pages (from-to)960-967
<mark>Original language</mark>English


The aim of this study was to investigate whether gluconeogenesis catalysed by phosphoenolpyruvate carboxykinase (PEPCK) occurs during leaf senescence. This was addressed by determining changes in the abundance and intercellular location of enzymes necessary for gluconeogenesis during the senescence of barley leaves and cucumber cotyledons. PEPCK was never present in barley leaves, despite the presence of large amounts of isocitrate lyase (ICL), a key enzyme of the glyoxylate cycle, and of its product, glyoxylate. Although PEPCK was present in non-senescent cucumber cotyledons, its abundance declined during senescence. Throughout senescence, PEPCK was only present in the trichomes and vasculature, whereas ICL was located in mesophyll cells. Pyruvate,Pi dikinase (PPDK) which, in concert with NAD(P)-malic enzyme, is also capable of catalysing gluconeogenesis, was present in non-senescent barley leaves and cucumber cotyledons, but in both plants its abundance decreased greatly during senescence. The abundance of ICL was greatly reduced in senescing detached barley leaves by either illumination or by co-incubation with sucrose, and greatly increased in darkened attached barley leaves. These results argue against the large-scale occurrence of gluconeogenesis during senescence catalysed either by PEPCK or PPDK. In cucumber cotyledons, PEPCK may play a role in metabolic processes linked to the export of amino acids, a role in which phosphoenolpyruvate carboxylase may also be involved. The amount of ICL was increased by starvation and during senescence may function in the conversion of lipids to organic acids, which are then utilised in the mobilisation of amino acids from leaf protein.