Unraveling the function of the two Entner-Doudoroff branches in the thermoacidophilic Crenarchaeon Sulfolobus solfataricus P2

FEBS J. 2013 Feb;280(4):1126-38. doi: 10.1111/febs.12106. Epub 2013 Jan 31.


Sulfolobus solfataricus P2 is a thermoacidophilic archaeon that metabolizes glucose and galactose via an unusual branched Entner-Doudoroff (ED) pathway, which is characterized by a non-phosphorylative (np) and a semi-phosphorylative (sp) branch. However, so far the physiological significance of the two pathway branches is unknown. In order to address these questions two key enzymes of the branched ED pathway, the class II glycerate kinase (GK) of the np-ED branch and the 2-keto-3-deoxygluconate kinase (KDGK) of the sp-ED branch in S. solfataricus, were investigated. GK was recombinantly purified and characterized with respect to its kinetic properties. Mg(2+) dependent Sso-GK (glycerate + ATP → 2-phosphoglycerate + ADP) showed unusual regulatory properties, i.e. substrate inhibition and cooperativity by D-glycerate and ATP, and a substrate-inhibition model was established fitting closely to the experimental data. Furthermore, deletion of the sp-ED key enzyme KDGK in S. solfataricus PBL2025 resulted in a similar growth phenotype on glucose as substrate compared with the wild-type. In contrast, the mutant showed strongly increased concentrations of np-ED intermediates whereas the hexose and pentose phosphates as well as trehalose were decreased. Together the results indicate (a) that the np-ED pathway is able to compensate for the missing sp-ED branch in glucose catabolism, (b) that in addition to its catabolic function the sp-ED pathway has an additional although not essential role in providing sugar phosphates for anabolism/gluconeogenesis and (c) that GK, with its unusual regulatory properties, seems to play a major role in controlling the flux between the glycolytic np-ED and the glycolytic/gluconeogenetic sp-ED pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Archaeal Proteins / biosynthesis
  • Archaeal Proteins / chemistry
  • Archaeal Proteins / genetics
  • Cloning, Molecular
  • Gene Deletion
  • Glyceric Acids / chemistry
  • Glycolysis
  • Hexokinase / chemistry
  • Kinetics
  • Metabolic Networks and Pathways*
  • Metabolome
  • Phosphorylation
  • Phosphotransferases (Alcohol Group Acceptor) / biosynthesis
  • Phosphotransferases (Alcohol Group Acceptor) / chemistry
  • Phosphotransferases (Alcohol Group Acceptor) / genetics
  • Sulfolobus solfataricus / enzymology*
  • Sulfolobus solfataricus / growth & development
  • Sulfolobus solfataricus / metabolism


  • Archaeal Proteins
  • Glyceric Acids
  • Phosphotransferases (Alcohol Group Acceptor)
  • Hexokinase
  • glycerate kinase
  • 2-keto-3-deoxygluconokinase