A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus

Background: Hexokinase and glucokinase enzymes are ubiquitously expressed and use ATP and ADP as substrates in mammalian systems and a variety of polyphosphate substrates and/or ATP in some eukaryotic and microbial systems. Polyphosphate synthesising or utilizing enzymes are widely expressed in micr...

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Main Authors: Ali, Antasar, Wathes, D. Claire, Swali, Angelina, Burns, Helena, Burns, Shamus
Format: Article
Published: Elsevier 2017
Subjects:
Online Access:https://eprints.nottingham.ac.uk/47552/
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author Ali, Antasar
Wathes, D. Claire
Swali, Angelina
Burns, Helena
Burns, Shamus
author_facet Ali, Antasar
Wathes, D. Claire
Swali, Angelina
Burns, Helena
Burns, Shamus
author_sort Ali, Antasar
building Nottingham Research Data Repository
collection Online Access
description Background: Hexokinase and glucokinase enzymes are ubiquitously expressed and use ATP and ADP as substrates in mammalian systems and a variety of polyphosphate substrates and/or ATP in some eukaryotic and microbial systems. Polyphosphate synthesising or utilizing enzymes are widely expressed in microbial systems but have not been reported in mammalian systems, despite the presence of polyphosphate in mammalian cells. Only two micro-organisms have previously been shown to express an enzyme that uses polyphosphate exclusively. Methods: A variety of experimental approaches, including NMR and NAD-linked assay systems were used to conduct a biochemical investigation of polyphosphate dependent glucokinase activity in mammalian tissues. Results: A novel mammalian glucokinase, highly responsive to hexametaphosphate (HMP) but not ATP or ADP as a phosphoryl donor is present in the nuclei of mammalian hepatocytes. The liver enzyme exhibited sigmoidal kinetics with respect to glucose with a S0.5 of 12 mM, similar to the known kinetics of mammalian ATP-glucokinase. The Km for HMP (0.5 mM) was also similar to that of phosphoryl donors for mammalian ATP-glucokinases. The new enzyme was inhibited by several nucleotide phosphates. Conclusions: We report the discovery of a polyphosphate-dependent enzyme system in mammalian cells with kinetics similar to established ATP-dependent glucokinase, also known to have a nuclear location. The kinetics suggest possible regulatory or redox protective roles. General significance: The role of polyphosphate in mammalian systems has remained an enigma for decades, and the present report describes progress on the significance of this compound in intracellular metabolism in mammals.
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spelling nottingham-475522020-05-04T19:20:14Z https://eprints.nottingham.ac.uk/47552/ A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus Ali, Antasar Wathes, D. Claire Swali, Angelina Burns, Helena Burns, Shamus Background: Hexokinase and glucokinase enzymes are ubiquitously expressed and use ATP and ADP as substrates in mammalian systems and a variety of polyphosphate substrates and/or ATP in some eukaryotic and microbial systems. Polyphosphate synthesising or utilizing enzymes are widely expressed in microbial systems but have not been reported in mammalian systems, despite the presence of polyphosphate in mammalian cells. Only two micro-organisms have previously been shown to express an enzyme that uses polyphosphate exclusively. Methods: A variety of experimental approaches, including NMR and NAD-linked assay systems were used to conduct a biochemical investigation of polyphosphate dependent glucokinase activity in mammalian tissues. Results: A novel mammalian glucokinase, highly responsive to hexametaphosphate (HMP) but not ATP or ADP as a phosphoryl donor is present in the nuclei of mammalian hepatocytes. The liver enzyme exhibited sigmoidal kinetics with respect to glucose with a S0.5 of 12 mM, similar to the known kinetics of mammalian ATP-glucokinase. The Km for HMP (0.5 mM) was also similar to that of phosphoryl donors for mammalian ATP-glucokinases. The new enzyme was inhibited by several nucleotide phosphates. Conclusions: We report the discovery of a polyphosphate-dependent enzyme system in mammalian cells with kinetics similar to established ATP-dependent glucokinase, also known to have a nuclear location. The kinetics suggest possible regulatory or redox protective roles. General significance: The role of polyphosphate in mammalian systems has remained an enigma for decades, and the present report describes progress on the significance of this compound in intracellular metabolism in mammals. Elsevier 2017-12-01 Article PeerReviewed Ali, Antasar, Wathes, D. Claire, Swali, Angelina, Burns, Helena and Burns, Shamus (2017) A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus. Biochemistry and Biophysics Reports, 12 . pp. 151-157. ISSN 2405-5808 Glucokinase ; Hexokinase ; Polyphosphate ; Evolution http://www.sciencedirect.com/science/article/pii/S2405580817301929?via%3Dihub doi:10.1016/j.bbrep.2017.09.004 doi:10.1016/j.bbrep.2017.09.004
spellingShingle Glucokinase ; Hexokinase ; Polyphosphate ; Evolution
Ali, Antasar
Wathes, D. Claire
Swali, Angelina
Burns, Helena
Burns, Shamus
A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus
title A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus
title_full A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus
title_fullStr A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus
title_full_unstemmed A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus
title_short A novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus
title_sort novel mammalian glucokinase exhibiting exclusive inorganic polyphosphate dependence in the cell nucleus
topic Glucokinase ; Hexokinase ; Polyphosphate ; Evolution
url https://eprints.nottingham.ac.uk/47552/
https://eprints.nottingham.ac.uk/47552/
https://eprints.nottingham.ac.uk/47552/