Literature DB >> 7706272

Adenylate kinase-catalyzed phosphoryl transfer couples ATP utilization with its generation by glycolysis in intact muscle.

R J Zeleznikar1, P P Dzeja, N D Goldberg.   

Abstract

We previously suggested that an importance of adenylate kinase (AdK) in skeletal muscle is to function as a high energy phosphoryl transfer system regulating ATP generation in correspondence with its consumption by specific cellular processes. The present experiments are intended to define the ATP-generating system coupled to and regulated by AdK-catalyzed phosphotransfer in skeletal muscle and also to examine the relationship between AdK- and creatine kinase (CK)-catalyzed phosphotransfer. Rates of phosphoryl transfer catalyzed by AdK were assessed in intact, isolated rat diaphragm by determining rates of AMP phosphorylation with endogenously generated [gamma-18O]ATP under conditions of altered anaerobic and aerobic ATP production. AdK-catalyzed phosphoryl transfer rates accelerated incrementally up to 12-fold in direct proportion to stimulated contractile frequency in parallel with equivalent increases in rates of ATP generation by lactate producing glycolysis. Stoichiometric equivalent increases of AdK-catalyzed phosphotransfer and anaerobic ATP production also occurred up to more than 20-fold when oxidative phosphorylation was impaired by either O2 deprivation or treatment with KCN or p-(trifluoromethoxy)-phenylhydrazone. These enhanced rates of AMP phosphorylation were balanced by virtually identically increased rates of AdK-catalyzed generation of AMP. This AMP was traced to arise from AdK-catalyzed phosphotransfer involving ADP generated by a muscle ATPase. Increased AdK-catalyzed phosphotransfer paired with the apparent compensatory increase in ATP generation by anaerobic glycolysis in oxygen-deprived muscle occurred coincident with diminished rates of CK-catalyzed phosphoryl transfer indicative of a pairing between oxidatively produced ATP and CK-catalyzed phosphotransfer. A metabolic model consistent with these results and conforming to the Mitchell general principle of vectorial ligand conduction is suggested.

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Year:  1995        PMID: 7706272     DOI: 10.1074/jbc.270.13.7311

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  34 in total

1.  Reduced activity of enzymes coupling ATP-generating with ATP-consuming processes in the failing myocardium.

Authors:  P P Dzeja; D Pucar; M M Redfield; J C Burnett; A Terzic
Journal:  Mol Cell Biochem       Date:  1999-11       Impact factor: 3.396

2.  Mapping hypoxia-induced bioenergetic rearrangements and metabolic signaling by 18O-assisted 31P NMR and 1H NMR spectroscopy.

Authors:  Darko Pucar; Petras P Dzeja; Peter Bast; Richard J Gumina; Carmen Drahl; Lynette Lim; Nenad Juranic; Slobodan Macura; Andre Terzic
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

Review 3.  CK flux or direct ATP transfer: versatility of energy transfer pathways evidenced by NMR in the perfused heart.

Authors:  F Joubert; P Mateo; B Gillet; J C Beloeil; J L Mazet; J A Hoerter
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

4.  Two structurally distinct and spatially compartmentalized adenylate kinases are expressed from the AK1 gene in mouse brain.

Authors:  Edwin Janssen; Jan Kuiper; Denice Hodgson; Leonid V Zingman; Alexey E Alekseev; Andre Terzic; Bé Wieringa
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

Review 5.  KATP Channels in the Cardiovascular System.

Authors:  Monique N Foster; William A Coetzee
Journal:  Physiol Rev       Date:  2016-01       Impact factor: 37.312

6.  Ca2+-activated myosin-ATPases, creatine and adenylate kinases regulate mitochondrial function according to myofibre type in rabbit.

Authors:  N Gueguen; L Lefaucheur; P Ecolan; M Fillaut; P Herpin
Journal:  J Physiol       Date:  2005-02-24       Impact factor: 5.182

Review 7.  31P-NMR-measured creatine kinase reaction flux in muscle: a caveat!

Authors:  T Wallimann
Journal:  J Muscle Res Cell Motil       Date:  1996-04       Impact factor: 2.698

8.  Theoretical modelling of some spatial and temporal aspects of the mitochondrion/creatine kinase/myofibril system in muscle.

Authors:  G J Kemp; D N Manners; J F Clark; M E Bastin; G K Radda
Journal:  Mol Cell Biochem       Date:  1998-07       Impact factor: 3.396

9.  Cytoarchitectural and metabolic adaptations in muscles with mitochondrial and cytosolic creatine kinase deficiencies.

Authors:  K Steeghs; F Oerlemans; A de Haan; A Heerschap; L Verdoodt; M de Bie; W Ruitenbeek; A Benders; C Jost; J van Deursen; P Tullson; R Terjung; P Jap; W Jacob; D Pette; B Wieringa
Journal:  Mol Cell Biochem       Date:  1998-07       Impact factor: 3.396

10.  Identification and biochemical characterization of adenylate kinase 1 from Clonorchis sinensis.

Authors:  Pei Liang; Fan Zhang; Wenjun Chen; Xuchu Hu; Yan Huang; Shan Li; Mengyu Ren; Lei He; Ran Li; Xuerong Li; Jin Xu; Zhongdao Wu; Gang Lu; Xinbing Yu
Journal:  Parasitol Res       Date:  2013-02-28       Impact factor: 2.289

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