Literature DB >> 168880

Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.

B Lederer, F Van Hoof, G Van den Berghe, H Hers.   

Abstract

1. The properties of phosphorylase a, phosphorylase b, phosphorylase kinase and phosphorylase phosphatase present in a human haemolysate were investigated. The two forms of phosphorylase have the same affinity for glucose 1-phosphate but greatly differ in Vmax. Phosphorylase b is only partially stimulated by AMP, since, in the presence of the nucleotide, it is about tenfold less active than phosphorylase a. In a fresh human haemolysate phosphorylase is mostly in the b form; it is converted into phosphorylase a by incubation at 20degreesC, and this reaction is stimulated by glycogen and cyclic AMP. Once activated, the enzyme can be inactivated after filtration of the haemolysate on Sephadex G-25. This inactivation is stimulated by caffeine and glucose and inhibited by AMP and fluoride. The phosphorylase kinase present in the haemolysate can also be measured by the rate of activation of added muscle phosphorylase b, on addition of ATP and Mg2+. 2. The activity of phosphorylase kinase was measured in haemolysates obtained from a series of patients who had been classified as suffering from type VI glycogenosis. In nine patients, all boys, an almost complete deficiency of phosphorylase kinase was observed in the haemolysate and, when it could be assayed, in the liver. A residual activity, about 20% of normal, was found in the leucocyte fraction, whereas the enzyme activity was normal in the muscle. These patients suffer from the sex-linked phosphorylase kinase deficiency previously described by others. Two pairs of siblings, each time brother and sister, displayed a partial deficiency of phosphorylase kinase in the haemolysate and leucocytes and an almost complete deficiency in the liver. This is considered as being the autosomal form of phosphorylase kinase deficiency. Other patients were characterized by a low activity of total (a+b) phosphorylase and a normal or high activity of phosphorylase kinase in their haemolysate.

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Year:  1975        PMID: 168880      PMCID: PMC1165371          DOI: 10.1042/bj1470023

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  38 in total

1.  PURIFICATION AND PROPERTIES OF RABBIT SKELETAL MUSCLE PHOSPHORYLASE B KINASE.

Authors:  E G KREBS; D S LOVE; G E BRATVOLD; K A TRAYSER; W L MEYER; E H FISCHER
Journal:  Biochemistry       Date:  1964-08       Impact factor: 3.162

2.  PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.

Authors:  S TARUI; G OKUNO; Y IKURA; T TANAKA; M SUDA; M NISHIKAWA
Journal:  Biochem Biophys Res Commun       Date:  1965-05-03       Impact factor: 3.575

3.  [Heterogeneity of glycogenosis type VI. Study of leukocyte phosphorylase activity in 2 families].

Authors:  P Guibaud; M Mathieu
Journal:  Arch Fr Pediatr       Date:  1972-12

4.  Glycogen storage disease type IX: benign glycogenosis of liver and hepatic phosphorylase kinase deficiency.

Authors:  R N Schimke; R M Zakheim; R C Corder; G Hug
Journal:  J Pediatr       Date:  1973-12       Impact factor: 4.406

5.  Inhibition of the phosphorylase kinase catalyzed reaction by glucose-6-P.

Authors:  J I Tu; D J Graves
Journal:  Biochem Biophys Res Commun       Date:  1973-07-02       Impact factor: 3.575

6.  Phosphorylase isoenzymes in tissues: prevalence of the liver type in man.

Authors:  D Proux; J C Dreyfus
Journal:  Clin Chim Acta       Date:  1973-10-12       Impact factor: 3.786

7.  Isoenzymes of glycogen phosphorylase in human leukocytes and platelets: relation to muscle phosphorylase.

Authors:  A A Yunis; G K Arimura
Journal:  Biochem Biophys Res Commun       Date:  1968-10-10       Impact factor: 3.575

8.  The regulation of skeletal muscle phosphorylase kinase by Ca2+.

Authors:  C O Brostrom; F L Hunkeler; E G Krebs
Journal:  J Biol Chem       Date:  1971-04-10       Impact factor: 5.157

9.  Phosphorylase kinase of the liver: deficiency in a girl with increased hepatic glycogen.

Authors:  G Hug; W K Schubert; G Chuck
Journal:  Science       Date:  1966-09-23       Impact factor: 47.728

10.  Type VI glycogenosis: biochemical demonstration of liver phosphorylase deficiency.

Authors:  G Hug; W K Schubert
Journal:  Biochem Biophys Res Commun       Date:  1970-12-09       Impact factor: 3.575

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  29 in total

1.  cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis.

Authors:  J J Davidson; T Ozçelik; C Hamacher; P J Willems; U Francke; M W Kilimann
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-15       Impact factor: 11.205

Review 2.  Phosphorylase b kinase deficiency in man: a review.

Authors:  I E Van den Berg; R Berger
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Elevated serum biotinidase activity in hepatic glycogen storage disorders--a convenient biomarker.

Authors:  P Paesold-Burda; M R Baumgartner; R Santer; N U Bosshard; B Steinmann
Journal:  J Inherit Metab Dis       Date:  2007-11-12       Impact factor: 4.982

4.  An optimized assay of phosphorylase kinase in crude liver preparations.

Authors:  K Uyttenhove; M Bollen; W Stalmans
Journal:  Biochem J       Date:  1991-09-15       Impact factor: 3.857

5.  Hepatic phosphorylase b kinase deficiency with normal enzyme activity in leukocytes and erythrocytes.

Authors:  H D Bakker; J A Taminiau; J E van den Berg; R Berger
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

6.  The natural history of liver glycogenosis due to phosphorylase kinase deficiency: a longitudinal study of 41 patients.

Authors:  P J Willems; W J Gerver; R Berger; J Fernandes
Journal:  Eur J Pediatr       Date:  1990-01       Impact factor: 3.183

7.  Neonatal-onset severe recurrent hypoglycaemia in an infant with hepatic phosphorylase kinase deficiency with normal enzyme activity in erythrocytes.

Authors:  C Fiçicioğlu; A Aydin; S Mikla; H Cam; Y Shin
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

8.  Mutations in the liver glycogen phosphorylase gene (PYGL) underlying glycogenosis type VI.

Authors:  B Burwinkel; H D Bakker; E Herschkovitz; S W Moses; Y S Shin; M W Kilimann
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

9.  A female case of type VIII glycogenosis who developed cirrhosis of the liver and hepatocellular tumor.

Authors:  S Shiomi; Y Saeki; K Kim; S Nishiguchi; S Seki; T Kuroki; K Kobayashi; S Harihara; M Owada
Journal:  Gastroenterol Jpn       Date:  1989-12

10.  Phosphorylase b kinase deficiency in a boy with glycogenosis affecting both liver and muscle.

Authors:  M Madlom; G T Besley; P T Cohen; V J Marrian
Journal:  Eur J Pediatr       Date:  1989-10       Impact factor: 3.183

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