The role of glutamine synthetase in energy production and glutamine metabolism during oxidative stress

• DOI: 10.1007/s10482-017-0829-3
• Publication Date: 2017-01-17T12:27:53Z
• Authors: Nohaiah Aldarini; Azhar A. Alhasawi; Sean C. Thomas; Vasu D. Appanna
• Keywords: Pseudomonas fluorescens; Adenosine triphosphate; Adenine nucleotide; Glutamine amidotransferase; Acetate kinase

Oxidative stress is known to severely impede aerobic adenosine triphosphate (ATP) synthesis. However, the metabolically-versatile Pseudomonas fluorescens survives this challenge by invoking alternative ATP-generating networks. When grown in a medium with glutamine as the sole organic nutrient in the presence of H2O2, the microbe utilizes glutamine synthetase (GS) to modulate its energy budget. The activity of this enzyme that mediates the release of energy stored in glutamine was sharply increased in the stressed cells compared to the controls. The enhanced activities of such enzymes as acetate kinase, adenylate kinase and nucleotide diphosphate kinase ensured the efficacy of this ATP producing-machine by transferring the high energy phosphate. The elevated amounts of phosphoenol pyruvate carboxylase and pyruvate orthophosphate dikinase recorded in the H2O2 exposed cells provided another route to ATP independent of the reduction of O2. This is the first demonstration of a metabolic pathway involving GS dedicated to ATP synthesis. The phospho-transfer network that is pivotal to the survival of the microorganism under oxidative stress may reveal therapeutic targets against infectious microbes reliant on glutamine for their proliferation.