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1.
Clin Chem ; 47(3): 477-85, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11238300

ABSTRACT

BACKGROUND: Dopa-responsive dystonia (DRD) and tetrahydrobiopterin (BH4) defects are inherited disorders characterized by monoamine neurotransmitter deficiency with decreased activity of one of the BH4-metabolizing enzymes. The aim of the study was to determine the utility of cultured skin fibroblasts for the diagnosis of these diseases. METHODS: Neopterin and biopterin production and GTP cyclohydrolase I (GTPCH) activity were measured in cytokine-stimulated fibroblasts; 6-pyruvoyltetrahydropterin synthase (PTPS), sepiapterin reductase (SR), and dihydropteridine reductase (DHPR) activities were measured in unstimulated fibroblasts. We examined 8 patients with DRD, 3 with autosomal recessive GTPCH deficiency, 7 with PTPS deficiency, 3 with DHPR deficiency, and 49 controls (35 fibroblast and 14 amniocyte samples). RESULTS: Fibroblasts from patients with DRD and autosomal recessive GTPCH deficiency showed reduced GTPCH activity (15.4% and 30.7% of normal activity, respectively) compared with controls (P < 0.001). Neopterin production was very low and biopterin production was reduced in both disorders. PTPS- and DHPR-deficient cells showed no enzyme activities; in PTPS deficiency the pattern of pterin production was typical (neopterin, 334-734 pmol/mg; controls, 18-98 pmol/mg; biopterin, 0 pmol/mg; controls, 154-303 pmol/mg). Reference values of all enzyme activities and pterin production were measured in fibroblasts and also in amniocytes for prenatal diagnosis. CONCLUSIONS: Cultured skin fibroblasts are a useful tool in the diagnosis of BH4 deficiencies. Intracellular neopterin and biopterin concentrations and GTPCH activity in cytokine-stimulated fibroblasts are particularly helpful in diagnosing patients with DRD.


Subject(s)
Biopterins/analogs & derivatives , Biopterins/deficiency , Dihydroxyphenylalanine/therapeutic use , Dopamine Agents/therapeutic use , Dystonia/diagnosis , Fibroblasts/metabolism , Metabolism, Inborn Errors/diagnosis , Alcohol Oxidoreductases/metabolism , Biopterins/biosynthesis , Biopterins/metabolism , Cell Extracts , Cells, Cultured , Cytokines/pharmacology , Dihydropteridine Reductase/metabolism , Dystonia/drug therapy , Female , Fibroblasts/cytology , Fibroblasts/enzymology , GTP Cyclohydrolase/metabolism , Humans , Male , Neopterin/biosynthesis , Phosphorus-Oxygen Lyases/metabolism , Reference Values , Skin/cytology
2.
J Biol Chem ; 274(44): 31341-8, 1999 Oct 29.
Article in English | MEDLINE | ID: mdl-10531334

ABSTRACT

6-Pyruvoyltetrahydropterin synthase (PTPS) participates in tetrahydrobiopterin cofactor biosynthesis. We previously identified in a PTPS-deficient patient an inactive PTPS allele with an Arg(16) to Cys codon mutation. Arg(16) is located in the protein surface exposed phosphorylation motif Arg(16)-Arg-Ile-Ser, with Ser(19) as the putative phosphorylation site for serine-threonine protein kinases. Purification of recombinant PTPS-S19A from bacterial cells resulted in an active enzyme (k(cat)/K(m) = 6.4 x 10(3) M(-1) s(-1)), which was similar to wild-type PTPS (k(cat)/K(m) = 4.1 x 10(3) M(-1) s(-1)). In assays with purified enzymes, wild-type but not PTPS-S19A was a specific substrate for the cGMP-dependent protein kinase (cGK) type I and II. Upon expression in COS-1 cells, PTPS-S19A was stable but not phosphorylated and had a reduced activity of approximately 33% in comparison to wild-type PTPS. Extracts from several human cell lines, including brain, contained a kinase that bound to and phosphorylated immobilized wild-type, but not mutant PTPS. Addition of cGMP stimulated phosphotransferase activity 2-fold. Extracts from transfected COS-1 cells overexpressing cGKII stimulated Ser(19) phosphorylation more than 100-fold, but only 4-fold from cGKI overexpressing cells. Moreover, fibroblast extracts from mice lacking cGKII exhibited significantly reduced phosphorylation of PTPS. These results suggest that Ser(19) of human PTPS may be a substrate for cGKII phosphorylation also in vivo, a modification that is essential for normal activity.


Subject(s)
Amino Acid Metabolism, Inborn Errors/genetics , Carbazoles , Cyclic GMP-Dependent Protein Kinases/metabolism , Indoles , Phosphorus-Oxygen Lyases/metabolism , Serine/metabolism , Alkaloids/pharmacology , Amino Acid Metabolism, Inborn Errors/enzymology , Amino Acid Sequence , Animals , COS Cells , Consensus Sequence , Cyclic GMP-Dependent Protein Kinase Type II , Cyclic GMP-Dependent Protein Kinases/antagonists & inhibitors , Cyclic GMP-Dependent Protein Kinases/genetics , Fibroblasts/enzymology , Humans , Mice , Mice, Knockout , Molecular Sequence Data , Mutation , Phosphorus-Oxygen Lyases/deficiency , Phosphorus-Oxygen Lyases/genetics , Phosphorylation , Protein Serine-Threonine Kinases , Recombinant Proteins/metabolism , Skin/enzymology , Staurosporine/pharmacology
3.
J Mol Biol ; 286(3): 851-60, 1999 Feb 26.
Article in English | MEDLINE | ID: mdl-10024455

ABSTRACT

The enzyme 6-pyruvoyl tetrahydropterin synthase (PTPS) catalyses the second step in the de novo biosynthesis of tetrahydrobiopterin, the conversion of dihydroneopterin triphosphate to 6-pyruvoyl tetrahydropterin. The Zn and Mg-dependent reaction includes a triphosphate elimination, a stereospecific reduction of the N5-C6 double bond and the oxidation of both side-chain hydroxyl groups. The crystal structure of the inactive mutant Cys42Ala of PTPS in complex with its natural substrate dihydroneopterinetriphosphate was determined at 1.9 A resolution. Additionally, the uncomplexed enzyme was refined to 2.0 A resolution. The active site of PTPS consists of the pterin-anchoring Glu A107 neighboured by two catalytic motifs: a Zn(II) binding site and an intersubunit catalytic triad formed by Cys A42, Asp B88 and His B89. In the free enzyme the Zn(II) is in tetravalent co-ordination with three histidine ligands and a water molecule. In the complex the water is replaced by the two substrate side-chain hydroxyl groups yielding a penta-co-ordinated Zn(II) ion. The Zn(II) ion plays a crucial role in catalysis. It activates the protons of the substrate, stabilizes the intermediates and disfavours the breaking of the C1'C2' bond in the pyruvoyl side-chain. Cys A42 is activated by His B89 and Asp B88 for proton abstraction from the two different substrate side-chain atoms C1', and C2'. Replacing Ala A42 in the mutant structure by the wild-type Cys by modelling shows that the C1' and C2' substrate side-chain protons are at equal distances to Cys A42 Sgamma. The basicity of Cys A42 may be increased by a catalytic triad His B89 and Asp B88. The active site of PTPS seems to be optimised to carry out proton abstractions from two different side-chain C1' and C2' atoms, with no obvious preference for one of them. Kinetic studies with dihydroneopterin monophosphate reveal that the triphosphate moiety of the substrate is necessary for enzyme specifity.


Subject(s)
Liver/enzymology , Phosphorus-Oxygen Lyases/chemistry , Animals , Binding Sites , Biopterins/analogs & derivatives , Biopterins/biosynthesis , Crystallography, X-Ray , Kinetics , Models, Molecular , Molecular Structure , Mutation/genetics , Protein Structure, Secondary , Rats , Zinc/chemistry
4.
Hum Gene Ther ; 7(13): 1587-93, 1996 Aug 20.
Article in English | MEDLINE | ID: mdl-8864759

ABSTRACT

Tetrahydrobiopterin (BH4) deficiency, a variant form of hyperphenylalaninemia with progressive neurological dysfunction, is primarily caused by autosomal recessive mutations in the gene encoding the 6-pyruvoyl-tetrahydropterin synthase (PTPS). PTPS is a biosynthetic enzyme for the BH4 co-factor, and its deficiency is associated with a malfunction of the phenylalanine catabolism in the liver and a lack of biogenic amine neurotransmitters dopamine and serotonin in the brain. We have previously isolated the wild-type PTPS cDNA and identified several mutations responsible for a decreased enzyme in patients. This study reports the in vitro correction of BH4 deficiency by using retrovirus mediated transfer of the PTPS cDNA into primary fibroblast cultures established from different patients. The Bing packaging cell line was used for amphotropic virus production. Following PTPS gene transfer, stimulation with cytokines restored biosynthesis of BH4 in originally defective cells to values comparable to those of heterozygous fibroblasts from clinically healthy subjects. These results not only provide a direct proof that the mutations in PTPS were causative for the mutant phenotype, but they are also the first step toward gene therapy as a potential alternative approach to treat BH4 deficiency.


Subject(s)
Alcohol Oxidoreductases/metabolism , Biopterins/analogs & derivatives , Gene Transfer Techniques , Phosphorus-Oxygen Lyases , Retroviridae/metabolism , Biopterins/analysis , Biopterins/deficiency , Biopterins/metabolism , Blotting, Western , Cytokines/pharmacology , Fibroblasts , Genes, Reporter/genetics , Genetic Diseases, Inborn/therapy , Genetic Therapy/methods , Genetic Vectors/genetics , Humans , Neopterin , Phenylalanine/blood , Phenylalanine/metabolism , Retroviridae/genetics , Transfection/genetics , beta-Galactosidase/genetics , beta-Galactosidase/metabolism
5.
Clin Chim Acta ; 226(2): 159-69, 1994 May.
Article in English | MEDLINE | ID: mdl-7923811

ABSTRACT

Prenatal diagnosis of tetrahydrobiopterin (BH4) deficiency was undertaken by evaluating the pterin patterns in amniotic fluid and the specific enzyme activities in fetal or extrafetal tissues. This allowed the prenatal diagnosis in 19 pregnancies at risk. In 8 families with a child already affected by dihydropteridine reductase deficiency 4 fetuses were diagnosed as homozygotes and 4 as heterozygotes for the defect. In 11 families with a child affected by 6-pyruvoyl tetrahydropterin synthase deficiency 4 fetuses were homozygous, 4 heterozygous and 3 normal. This study also advanced our knowledge of tetrahydrobiopterin metabolism during fetal development. The key enzymes involved in the biosynthesis of BH4 are expressed early and allow the fetus to be autotrophous for its cofactor requirement. In a twin pregnancy, both fetuses were diagnosed to be heterozygotes for dihydropteridine reductase deficiency and primapterin (7-biopterin) in amniotic fluid was increased. This indicates that pterin-4 alpha-carbinolamine dehydratase activity seems to be differently expressed during fetal life. As a consequence, pterins detected in amniotic fluid are of fetal origin and 6- and 7-substituted pterins can be present in amniotic fluid in higher proportions when compared with other body fluids.


Subject(s)
Amniotic Fluid/chemistry , Biopterins/analogs & derivatives , Fetus/enzymology , Phosphorus-Oxygen Lyases , Prenatal Diagnosis/methods , Pterins/analysis , Alcohol Oxidoreductases/deficiency , Biopterins/analysis , Biopterins/deficiency , Female , GTP Cyclohydrolase/deficiency , Humans , Hydro-Lyases/deficiency , Neopterin , Phenylketonurias , Pregnancy , Xanthopterin/analysis
6.
Am J Hum Genet ; 54(5): 782-92, 1994 May.
Article in English | MEDLINE | ID: mdl-8178819

ABSTRACT

A variant type of hyperphenylalaninemia is caused by a deficiency of tetrahydrobiopterin (BH4), the obligatory cofactor for phenylalanine hydroxylase. The most frequent form of this cofactor deficiency is due to lack of 6-pyruvoyl-tetrahydropterin synthase (PTPS) activity, the second enzyme in the biosynthetic pathway for BH4. The human liver cDNA for PTPS was previously isolated, and the recombinant protein was found to be active when expressed in Escherichia coli. We now have investigated two patients for their molecular nature of this autosomal recessive disorder. Both patients were diagnosed as PTPS deficient, one with the central and one with the peripheral form, on the basis of an elevated serum phenylalanine concentration concomitant with lowered levels of urinary biopterin and PTPS activity in erythrocytes. Molecular analysis was performed on the patients' cultured primary skin fibroblasts. PTPS activities were found in vitro to be reduced to background activity. Direct cDNA sequence analysis using reverse transcriptase-PCR technology showed for the patient with the central from a homozygous G-to-A transition at codon 25, causing the replacement of an arginine by glutamine (R25Q). Expression of this mutant allele in E. coli revealed 14% activity when compared with the wild-type enzyme. The patient with the peripheral form exhibited compound heterozygosity, having on one allele a C-to-T transition resulting in the substitution of arginine 16 for cysteine (R16C) in the enzyme and having on the second allele a 14-bp deletion (delta 14bp), leading to a frameshift at lysine 120 and a premature stop codon (K120-->Stop). Heterologous expression of the enzyme with the single-amino-acid exchange R16C revealed only 7% enzyme activity, whereas expression of the deletion allele delta 14bp exhibited no detectable activity. All three mutations, R25Q, R16C, and K120-->Stop, affect evolutionarily conserved residues in PTPS, result in reduced enzymatic activity when reconstituted in E. coli, and are thus believed to be the molecular cause for the BH4 deficiency. This is the first report describing mutations in PTPS that lead to BH4 deficiency.


Subject(s)
Alcohol Oxidoreductases/genetics , Amino Acid Metabolism, Inborn Errors/genetics , Biopterins/analogs & derivatives , DNA/genetics , Phenylalanine/blood , Phosphorus-Oxygen Lyases , Point Mutation , Alcohol Oxidoreductases/deficiency , Alcohol Oxidoreductases/metabolism , Amino Acid Metabolism, Inborn Errors/enzymology , Amino Acid Sequence , Base Sequence , Biopterins/metabolism , Cloning, Molecular , DNA, Complementary/analysis , Escherichia coli , Female , Fibroblasts/enzymology , Gene Expression , Humans , Infant, Newborn , Male , Molecular Sequence Data , Oligonucleotide Probes , Polymerase Chain Reaction/methods , Reference Values
8.
Biochem Biophys Res Commun ; 189(3): 1437-43, 1992 Dec 30.
Article in English | MEDLINE | ID: mdl-1282802

ABSTRACT

6-Pyruvoyl-tetrahydropterin synthase (PTPS) is involved in the biosynthesis of tetrahydrobiopterin (BH4), an essential cofactor for enzymes such as the hepatic phenylalanine hydroxylase. BH4 deficiency causes malignant hyperphenylalaninemia. We cloned the human liver cDNA encoding PTPS. The coding region for PTPS contains 145 amino acids and predicts a polypeptide of 16'387 Da. The human amino acid sequence showed a 82% identity with the rat liver sequence. Expression of the cDNA in E. coli yielded the active enzyme and showed immunoreactivity with antibodies against the rat liver PTPS. This is the basis for the molecular understanding of BH4 deficiency in patients suffering from a defect in PTPS activity.


Subject(s)
Alcohol Oxidoreductases/genetics , Alcohol Oxidoreductases/metabolism , DNA/genetics , Liver/enzymology , Phosphorus-Oxygen Lyases , Alcohol Oxidoreductases/biosynthesis , Amino Acid Sequence , Animals , Base Sequence , Cloning, Molecular/methods , Electrophoresis, Polyacrylamide Gel , Gene Expression , Humans , Kinetics , Molecular Sequence Data , Molecular Weight , Oligodeoxyribonucleotides , Plasmids , Polymerase Chain Reaction , RNA/genetics , RNA/isolation & purification , Rats , Recombinant Proteins/biosynthesis , Recombinant Proteins/metabolism , Restriction Mapping , Salmon , Sequence Homology, Amino Acid
9.
Biochem Biophys Res Commun ; 182(2): 953-9, 1992 Jan 31.
Article in English | MEDLINE | ID: mdl-1734893

ABSTRACT

The most frequent variant of atypical phenylketonuria, an inborn error of metabolism, is characterized by a low activity of the 6-pyruvoyl tetrahydropterin synthase. We purified and characterized this enzyme from salmon liver known to contain high levels. After digestion, peptides were sequenced by tandem mass spectrometry and/or automated Edman microsequence analysis. Both a free amine terminus and an N-acetylated amine terminus were found, indicating the presence of two isoforms. The peptide sequences determined here have a high degree of homology with the protein sequence deduced from cDNA for rat 6-pyruvoyl tetrahydropterin synthase (1), however, the amine termini of these proteins differ significantly.


Subject(s)
Alcohol Oxidoreductases/chemistry , Liver/enzymology , Phosphorus-Oxygen Lyases , Alcohol Oxidoreductases/genetics , Alcohol Oxidoreductases/isolation & purification , Amino Acid Sequence , Animals , Chromatography, High Pressure Liquid , Electrophoresis, Gel, Two-Dimensional , Electrophoresis, Polyacrylamide Gel , Indicators and Reagents , Mass Spectrometry , Molecular Sequence Data , Molecular Weight , Peptide Fragments/isolation & purification , Rats , Salmon , Sequence Homology, Nucleic Acid
10.
Eur J Biochem ; 187(3): 651-6, 1990 Feb 14.
Article in English | MEDLINE | ID: mdl-2406138

ABSTRACT

The conversion of dihydroneopterin triphosphate in the presence of 6-pyruvoyl tetrahydropterin synthase was followed by 1H-NMR spectroscopy. The interpretation of the spectra of the product is unequivocal: they show formation of a tetrahydropterin system carrying a stereospecifically oriented substituent at the asymmetric C(6) atom. The spectra are compatible with formation of a (3')-CH3 function, and with complete removal of the 1' and 2' hydrogens of dihydroneopterin triphosphate. The fast-atom-bombardment/mass spectrometry study of the same product yields a [M + H]+ ion at m/z 238 compatible with the structure of 6-pyruvoyl tetrahydropterin. The data support the proposed structure of 6-pyruvoyl tetrahydropterin as a key intermediate in the biosynthesis of tetrahydrobiopterin.


Subject(s)
Biopterins/analogs & derivatives , Phosphorus-Oxygen Lyases , Pterins , Alcohol Oxidoreductases/metabolism , Biopterins/biosynthesis , Magnetic Resonance Spectroscopy , Mass Spectrometry , Models, Chemical , Neopterin/analogs & derivatives , Oxidation-Reduction , Pteridines/metabolism , Pterins/analysis , Stereoisomerism
11.
Biochem Biophys Res Commun ; 164(3): 1130-6, 1989 Nov 15.
Article in English | MEDLINE | ID: mdl-2511841

ABSTRACT

6-Pyruvoyl tetrahydropterin reductase has been implicated in the biosynthesis of tetrahydrobiopterin. Using immunochemical and biochemical techniques the purified human liver enzyme was shown to be identical to aldose reductase. This suggests that 6-pyruvoyl tetrahydropterin reductase may play an additional role in the reduction of aldehydes derived from the biogenic amine neuro-transmitters and corticosteroid hormones as well as in the pathogenesis of diabetic complications, as has been postulated for aldose reductase.


Subject(s)
Aldehyde Reductase/metabolism , Antibodies, Monoclonal , Ketone Oxidoreductases/metabolism , Liver/enzymology , Sugar Alcohol Dehydrogenases/metabolism , Aldehyde Reductase/immunology , Animals , Antibodies, Monoclonal/isolation & purification , Blotting, Western , Humans , Immunodiffusion , Ketone Oxidoreductases/immunology , Kinetics , Mice , Mice, Inbred BALB C/immunology , Substrate Specificity
13.
Biochem Biophys Res Commun ; 152(3): 1193-9, 1988 May 16.
Article in English | MEDLINE | ID: mdl-3377772

ABSTRACT

The first chemical synthesis of D-neopterin-3'-triphosphate and D-7,8-dihydroneopterin-3'-triphosphate is described. D-neopterin-3'-monophosphate was first 1'-2'-0-formylated with anhydrous formic acid, then activated with 1,1'-carbonyldiimidazole and phosphorylated with n-tributyl-ammonium pyrophosphate. The yield of 3'-NTP was 24%. D-7,8-dihydroneopterin-3'-triphosphate was obtained by chemical (hyposulfite) or catalytic (Pd:H2) reduction of 3'-NTP. Preparations from both reductions were fully active in two different enzymatic systems: synthesis of L-5,6,7,8-tetrahydrobiopterin and in the C-2'-epimerization reaction to L-7,8-dihydromonapterin-3'-triphosphate.


Subject(s)
Neopterin , Pteridines/chemical synthesis , Biopterins/analogs & derivatives , Biopterins/chemical synthesis , Methods
14.
Eur J Pediatr ; 147(1): 15-9, 1988 Jan.
Article in English | MEDLINE | ID: mdl-3276524

ABSTRACT

6-Pyruvoyl-tetrahydropterin synthase (PTS), a key enzyme in the synthesis of tetrahydrobiopterin in man, is defective in the most frequent variant of tetrahydrobiopterin-deficient hyperphenylalaninaemia (atypical phenylketonuria). An assay for PTS activity in erythrocytes was developed. It is based on the PTS-catalysed formation of tetrahydrobiopterin from dihydroneopterin triphosphate in the presence of magnesium, sepiapterin reductase, NADPH, dihydropteridine reductase, and NADH, and fluorimetric measurement of the product as biopterin by high performance liquid chromatography (HPLC) after oxidation with iodine. The PTS activity was higher in younger erythrocytes, including reticulocytes, than in older ones. Fetal erythrocytes showed approx. four times higher activities than those of adults. Using a more purified human liver sepiapterin reductase fraction which gave a lower yield than a crude preparation, adult controls (n = 8) showed a mean erythrocyte PTS activity of 17.6 (range 11.0-29.5) microU/g Hb. Nine of 11 patients with typical PTS deficiency showed activities between 0% and 8% of the mean of controls, and two of 11 showed 14% and 20%, respectively. The obligate heterozygotes (n = 16) had activities of 19% (range 8%-31%) of the mean of controls, i.e., significantly less than the expected 50%. Four patients with the "peripheral" type of the disease showed 7%-10% of the mean of controls. Thus, the assay did not distinguish between patients and heterozygotes in every family. The assay is well suited to the identification of heterozygotes of PTS deficiency in family studies.


Subject(s)
Alcohol Oxidoreductases/blood , Biopterins/analogs & derivatives , Biopterins/biosynthesis , Multienzyme Complexes/blood , Adult , Aging , Biopterins/deficiency , Child , Child, Preschool , Chromatography, High Pressure Liquid , Erythrocytes/metabolism , Humans , Infant , Middle Aged
15.
Eur J Pediatr ; 146(3): 228-32, 1987 May.
Article in English | MEDLINE | ID: mdl-3297709

ABSTRACT

Four patients in three families with "peripheral" tetrahydrobiopterin deficiency were investigated. They were characterized biochemically by a tetrahydrobiopterin-responsive hyperphenylalaninaemia, a high neopterin/biopterin ratio in urine and plasma, and normal or elevated concentrations of biopterin, homovanillic acid, and 5-hydroxyindole acetic acid in cerebrospinal fluid. From measurements of the activity of erythrocyte 6-pyruvoyl tetrahydropterin synthase (PTS, formerly called phosphate-eliminating enzyme) and phenylalanine loading tests in the patients and their parents, one patient was demonstrated to be heterozygous for PTS deficiency. The others were obviously genetic compounds (allelism) with incomplete PTS deficiency. Three of the children developed normally, two of them under treatment with tetrahydrobiopterin. In the latter two patients, significantly lower concentrations of biopterin, homovanillic acid, and 5-hydroxyindole acetic acid in cerebrospinal fluid were noted at age 7 months (when treatment was interrupted) than those observed at 3 and 5 weeks, respectively. The infant who is heterozygous for PTS deficiency was born small for gestational age and showed a moderately delayed psychomotor development. It is concluded that "peripheral" tetrahydrobiopterin deficiency is caused by a partial PTS deficiency with sufficient activity to cover the tetrahydrobiopterin requirement of tyrosine 3-hydroxylase and trytophan 5-hydroxylase in brain but not enough for phenylalanine 4-hydroxylase in liver. For therapy, tetrahydrobiopterin, 2-5 mg/kg in a single oral dose per day, is recommended to keep plasma phenylalanine normal. A careful observation of the mental development is indicated.


Subject(s)
Alcohol Oxidoreductases/deficiency , Biopterins/analogs & derivatives , Phenylalanine/blood , Phenylketonurias/genetics , Phosphorus-Oxygen Lyases , Biopterins/metabolism , Child, Preschool , Female , Heterozygote , Humans , Infant , Male , Phenylketonurias/metabolism , Pterins/metabolism
16.
Eur J Biochem ; 161(2): 295-302, 1986 Dec 01.
Article in English | MEDLINE | ID: mdl-3536512

ABSTRACT

6-Pyruvoyl-tetrahydropterin synthase, which catalyzes the first step in the conversion of 7,8-dihydroneopterin triphosphate to tetrahydrobiopterin, was purified approximately 140,000-fold to apparent homogeneity from human liver. The molecular mass of the enzyme is estimated to be 83 kDa. 7,8-Dihydroneopterin triphosphate was a substrate of the enzyme in the presence of Mg2+, and the pH optimum of the reaction was 7.5 in Tris HCl buffer. The Km value for 7,8-dihydroneopterin triphosphate was 10 microM. The product of this enzymatic reaction was the presumed intermediate 6-pyruvoyl-tetrahydropterin. This latter compound was converted to tetrahydrobiopterin in the presence of NADPH and partially purified sepiapterin reductase from human liver. The conditions and the effect of N-acetylserotonin on this reaction, and on the formation of the intermediates 6-(1'-hydroxy-2'-oxopropyl)-tetrahydropterin and 6-(1' oxo-2'-hydroxypropyl)-tetrahydropterin have been studied.


Subject(s)
Alcohol Oxidoreductases/isolation & purification , Biopterins/analogs & derivatives , Liver/enzymology , Phosphorus-Oxygen Lyases , Alcohol Oxidoreductases/metabolism , Biopterins/biosynthesis , Chromatography, High Pressure Liquid , Humans , Hydrogen-Ion Concentration , Molecular Weight
17.
Eur J Biochem ; 148(3): 413-9, 1985 May 02.
Article in English | MEDLINE | ID: mdl-3888618

ABSTRACT

The biosynthesis of tetrahydrobiopterin from either dihydroneopterin triphosphate, sepiapterin, dihydrosepiapterin or dihydrobiopterin was investigated using extracts from human liver, dihydrofolate reductase and purified sepiapterin reductase from human liver and rat erythrocytes. The incorporation of hydrogen in tetrahydrobiopterin was studied in either 2H2O or in H2O using unlabeled NAD(P)H or (R)-(4-2H)NAD(P)H or (S)-(4-2H)NAD(P)H. Dihydrofolate reductase catalyzed the transfer of the pro-R hydrogen of NAD(P)H during the reduction of 7,8-dihydrobiopterin to tetrahydrobiopterin. Sepiapterin reductase catalyzed the transfer of the pro-S hydrogen of NADPH during the reduction of sepiapterin to 7,8-dihydrobiopterin. In the presence of partially purified human liver extracts one hydrogen from the solvent is introduced at position C(6) and the 4-pro-S hydrogen from NADPH is incorporated at each of the C(1') and C(2') position of BH4. Label from the solvent is also introduced into position C(3'). These results suggest that dihydrofolate reductase is not involved in the biosynthesis of tetrahydrobiopterin from dihydroneopterin triphosphate. They are consistent with the assumption of the occurrence of a 6-pyruvoyl-tetrahydropterin intermediate, which is proposed to be formed upon triphosphate elimination from dihyroneopterin triphosphate, and via an intramolecular redox reaction. Our results suggest that the reduction of 6-pyruvoyl-tetrahydropterin might be catalyzed by sepiapterin reductase.


Subject(s)
Biopterins/biosynthesis , Erythrocytes/metabolism , Liver/metabolism , Pteridines/biosynthesis , Affinity Labels , Alcohol Oxidoreductases/metabolism , Animals , Biopterins/analogs & derivatives , Catalysis , Chromatography, High Pressure Liquid , Energy Transfer , Gas Chromatography-Mass Spectrometry , Humans , Hydrogen Bonding , Kinetics , NADP/metabolism , Oxidation-Reduction , Rats , Solvents , Stereoisomerism , Substrate Specificity , Tetrahydrofolate Dehydrogenase/metabolism
18.
Eur J Pediatr ; 144(1): 13-6, 1985 May.
Article in English | MEDLINE | ID: mdl-2990933

ABSTRACT

An assay for the phosphate-eliminating enzyme (PEE) activity in liver was developed which required only 5-10 mg tissue. PEE catalyses the elimination of inorganic triphosphate from dihydroneopterin triphosphate, which is the second and irreversible step in the biosynthesis of tetrahydrobiopterin (BH4). In the presence of substrate, magnesium, NADPH, and a sepiapterin reductase fraction from human liver, PEE catalysed the formation of BH4 which was measured by HPLC and electrochemical detection. In adult human liver, a PEE activity of 1.02 +/- 0.134 microU/mg protein (mean +/- 1 SD; n = 5) was observed. In liver needle biopsy material from five patients with defective biopterin biosynthesis, no PEE activity was found (less than 2% and 6% of the control values, respectively). The presence of an endogenous inhibitor was excluded. In a patient who died without definite diagnosis and in a patient with beta-thalassaemia liver PEE activity was increased. Sepiapterin reductase activity was present in all cases. Results indicate that in "dihydrobiopterin synthetase" deficiency, the most frequent of the rare BH4-deficient variants of hyperphenylalaninaemia, the molecular defect consists in a defect of PEE.


Subject(s)
Alcohol Oxidoreductases/deficiency , Liver/enzymology , Phenylketonurias/enzymology , Pyrophosphatases/metabolism , Adult , Alcohol Oxidoreductases/metabolism , Biopterins/analogs & derivatives , Biopterins/biosynthesis , Chemical Phenomena , Chemistry , Child , Child, Preschool , Female , Humans , Infant , Male , Neopterin/analogs & derivatives , Pteridines/metabolism
19.
Biochem Biophys Res Commun ; 127(1): 213-9, 1985 Feb 28.
Article in English | MEDLINE | ID: mdl-2983706

ABSTRACT

An enzyme catalyzing the elimination of triphosphate from 7,8-dihydroneopterin triphosphate in the presence of Mg2+ has been purified approx. 3000 fold from human liver. It has a molecular weight of approx. 63'000, a pI value of 4.4 - 4.6 and is stable at 80 degrees C for 5 min. This enzyme catalyzes the formation of tetrahydrobiopterin in the presence of sepiapterin reductase, Mg2+ and NADPH. It is thus possible, that it also catalyzes the internal oxidoreduction leading to formation of the intermediate 6-pyruvoyl-tetrahydropterin, suggesting that no further enzyme is obligatory for biosynthesis of tetrahydrobiopterin.


Subject(s)
Biopterins/biosynthesis , Liver/analysis , Pteridines/biosynthesis , Pyrophosphatases/isolation & purification , Biopterins/analogs & derivatives , Humans , Isoelectric Point , Magnesium/metabolism , Molecular Weight , NADP/metabolism , Neopterin/analogs & derivatives , Pteridines/metabolism , Pyrophosphatases/metabolism , Temperature , Time Factors
20.
J Inherit Metab Dis ; 8 Suppl 1: 28-33, 1985.
Article in English | MEDLINE | ID: mdl-3930838

ABSTRACT

The biosynthesis of tetrahydrobiopterin (BH4) from dihydroneopterin triphosphate (NH2P3) was studied in human liver extract. The phosphate-eliminating enzyme (PEE) was purified approximately 750-fold. The conversion of NH2P3 to BH4 was catalyzed by this enzyme in the presence of partially purified sepiapterin reductase. Mg2+ and NADPH. The PEE is heat stable when heated at 80 degrees C for 5 min. It has a molecular weight of 63 000 daltons. One possible intermediate 6-(1'-hydroxy-2'-oxopropyl)5,6,7,8-tetrahydropterin(2'-oxo-tetrahydropte rin) was formed upon incubation of BH4 in the presence of sepiapterin reductase and NADP+ at pH 9.0. Reduction of this compound with NaBD4 yielded monodeutero threo and erythro-BH4, the deuterium was incorporated at the 2' position. This and the UV spectra were consistent with a 2'-oxo-tetrahydropterin structure. Dihydrofolate reductase (DHFR) catalyzed the reduction of BH2 to BH4 and was found to be specific for the pro-R-NADPH side. The sepiapterin reductase catalyzed the transfer of the pro-S hydrogen of NADPH during the reduction of sepiapterin to BH2. In the presence of crude liver extracts the conversion of NH2P3 to BH4 requires NADPH. Two deuterium atoms were incorporated from (4S-2H)NADHP in the 1' and 2' position of the BH4 side chain. Incorporation of one hydrogen from the solvent was found at position C(6). These results are consistent with the occurrence of an intramolecular redox exchange between the pteridine nucleus and the side chain and formation of 6-pyruvoyl-5,6,7,8-tetrahydropterin(tetrahydro-1'-2'-dioxopterin) as intermediate.


Subject(s)
Biopterins/biosynthesis , Pteridines/biosynthesis , Alcohol Oxidoreductases/physiology , Biopterins/analogs & derivatives , Deuterium , Humans , In Vitro Techniques , Liver/metabolism , Neopterin/analogs & derivatives , Pteridines/metabolism , Tetrahydrofolate Dehydrogenase/physiology
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