Literature DB >> 3930842

Biotinidase deficiency: factors responsible for the increased biotin requirement.

E R Baumgartner, T Suormala, H Wick, J Bausch, J P Bonjour.   

Abstract

Inability to recycle biotin from endogenous biocytin in congenital biotinidase deficiency is associated with increased requirement of exogenous free biotin. We have observed that severe biotin depletion with clinical and biochemical consequences occurs within 12 days after birth in a newborn patient and within 15-20 days after withdrawal of biotin supplementation in four other patients. Our studies have shown that: Urinary loss of biotin and biocytin are major causes for this rapid biotin depletion. Intestinal absorption of biotin seems to be normal at least at the loading dose of 1.5 micrograms/kg. At normal or subnormal plasma biotin concentrations biocytin is found in low concentrations (below 1 nmol l-1) in plasma of patients but at much higher concentrations in urine (100-600 nmol l-1). An oral load of biocytin results in patients in unchanged biotin levels but in a marked rise of biocytin in plasma followed by rapid renal excretion of biocytin whereas in controls biotin levels in plasma increase rapidly and biocytin remains below detection levels.

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Year:  1985        PMID: 3930842     DOI: 10.1007/bf01800661

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  20 in total

1.  Biocytinase, an enzyme concerned with hydrolytic cleavage of biocytin.

Authors:  L D WRIGHT; C A DRISCOLL; W P BOGER
Journal:  Proc Soc Exp Biol Med       Date:  1954-06

2.  Mechanism of biotin-responsive combined carboxylase deficiency.

Authors:  H K Ghneim; K Bartlett
Journal:  Lancet       Date:  1982-05-22       Impact factor: 79.321

3.  Defective biotin absorption in multiple carboxylase deficiency.

Authors:  A Munnich; J M Saudubray; G Carré; F X Coudé; H Ogier; C Charpentier; J Frézal
Journal:  Lancet       Date:  1981-08-01       Impact factor: 79.321

4.  Stimulation of propionyl CoA and beta-methylcrotonyl CoA carboxylase activities in human leukocytes and cultured fibroblasts by biotin.

Authors:  B Wolf; L E Rosenberg
Journal:  Pediatr Res       Date:  1979-11       Impact factor: 3.756

5.  Detection of biocytin in urine of children with congenital biotinidase deficiency.

Authors:  J P Bonjour; J Bausch; T Suormala; E R Baumgartner
Journal:  Int J Vitam Nutr Res       Date:  1984       Impact factor: 1.784

6.  Impaired intestinal absorption of biotin in juvenile multiple carboxylase deficiency.

Authors:  J G Thoene; R Lemons; H Baker
Journal:  N Engl J Med       Date:  1983-03-17       Impact factor: 91.245

7.  Deficient biotinidase activity in late-onset multiple carboxylase deficiency.

Authors:  B Wolf; R E Grier; W D Parker; S I Goodman; R J Allen
Journal:  N Engl J Med       Date:  1983-01-20       Impact factor: 91.245

8.  Biotin deficiency in chicks fed a wheat-based diet.

Authors:  M Frigg; G Brubacher
Journal:  Int J Vitam Nutr Res       Date:  1976       Impact factor: 1.784

9.  Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.

Authors:  B J Burri; L Sweetman; W L Nyhan
Journal:  J Clin Invest       Date:  1981-12       Impact factor: 14.808

10.  Purification of biotinidase from human plasma and its activity on biotinyl peptides.

Authors:  D V Craft; N H Goss; N Chandramouli; H G Wood
Journal:  Biochemistry       Date:  1985-05-07       Impact factor: 3.162

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  6 in total

1.  Improved neuronal tract tracing with stable biocytin-derived neuroimaging agents.

Authors:  Anurag Mishra; Kirti Dhingra; Almut Schüz; Nikos K Logothetis; Santiago Canals
Journal:  ACS Chem Neurosci       Date:  2009-10-06       Impact factor: 4.418

2.  Development and characterization of a mouse with profound biotinidase deficiency: a biotin-responsive neurocutaneous disorder.

Authors:  Kirit Pindolia; Megan Jordan; Caiying Guo; Nell Matthews; Donald M Mock; Erin Strovel; Miriam Blitzer; Barry Wolf
Journal:  Mol Genet Metab       Date:  2010-10-13       Impact factor: 4.797

Review 3.  Enzyme studies in biotin-responsive disorders.

Authors:  K Bartlett; H K Ghneim; H J Stirk; H Wastell
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

4.  Cerebral metabolic change after treatment in biotinidase deficiency.

Authors:  I T Lott; S Lottenberg; W L Nyhan; M J Buchsbaum
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

Review 5.  The biochemical basis of mitochondrial diseases.

Authors:  H R Scholte
Journal:  J Bioenerg Biomembr       Date:  1988-04       Impact factor: 2.945

6.  Role of human serum biotinidase as biotin-binding protein.

Authors:  J Chauhan; K Dakshinamurti
Journal:  Biochem J       Date:  1988-11-15       Impact factor: 3.857

  6 in total

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