Literature DB >> 1355701

A coupled assay detecting defects in fibroblast isoleucine degradation distal to enoyl-CoA hydratase: application to 3-oxothiolase deficiency.

K M Gibson1, C F Lee, V Kamali, O Søvik.   

Abstract

We developed a coupled NaH14CO3 fixation assay to detect 3-oxothiolase deficiency in extracts of cultured human fibroblasts. Cell extracts were incubated with tiglyl-CoA, NAD, CoASH, ATP and NaH14CO3. The enzymatic activities of tiglyl-CoA (enoyl-CoA) hydratase, 2-methyl-3-hydroxybutyryl-CoA dehydrogenase and 2-methylacetoacetyl-CoA thiolase (3-oxothiolase) were coupled to produce propionyl-CoA. Propionyl-CoA produced in the assay was estimated by fixation of NaH14CO3 into [14C]methylmalonyl-CoA employing endogenous propionyl-CoA carboxylase. The control activity was 32 +/- 23 pmol/min per mg protein (+/- 1 S.D., range 7-94; 28 cell lines). Five known cases of 3-oxothiolase deficiency had a mean activity of 2% of the control; a sixth case of 3-oxothiolase deficiency was significantly higher at 27% of the mean control value. Coupled assay activity was also low (3% of control) in the cells from a patient with propionyl-CoA carboxylase deficiency.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1355701     DOI: 10.1016/s0009-8981(05)80007-5

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  6 in total

1.  A new case of 2-methylacetoacetyl-CoA thiolase deficiency?

Authors:  G Renom; M Fontaine; M O Rolland; J Duprey; P M Degand; D Dobbelaere
Journal:  J Inherit Metab Dis       Date:  2000-11       Impact factor: 4.982

2.  Metabolic coma with ketoacidosis and hyperglycaemia in 2-methylacetoacetyl-CoA thiolase deficiency.

Authors:  E Riudor; A Ribes; C Perez-Cerda; J A Arranz; J Mora; D Yeste; F Castello; B Christensen; O Sovik
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

3.  beta-Ketothiolase (2-methylacetoacetyl-coenzyme A thiolase) deficiency: identification of two patients in Israel.

Authors:  K M Gibson; O N Elpeleg; M J Bennett
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

4.  Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis.

Authors:  Stéphanie Paquay; Agnès Bourillon; Samia Pichard; Jean-François Benoist; Pascale de Lonlay; Dries Dobbelaere; Alain Fouilhoux; Nathalie Guffon; Isabelle Rouvet; François Labarthe; Karine Mention; Guy Touati; Vassili Valayannopoulos; Hélène Ogier de Baulny; Monique Elmaleh-Bergès; Cécile Acquaviva-Bourdain; Christine Vianey-Saban; Manuel Schiff
Journal:  J Inherit Metab Dis       Date:  2017-03-02       Impact factor: 4.982

5.  2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old man.

Authors:  S E Olpin; R J Pollitt; J McMenamin; N J Manning; G Besley; J P N Ruiter; R J A Wanders
Journal:  J Inherit Metab Dis       Date:  2002-10       Impact factor: 4.982

Review 6.  Screening for defects of branched-chain amino acid metabolism.

Authors:  K M Gibson; C F Lee; G F Hoffmann
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.