Literature DB >> 7150615

The existence of an inner-membrane-bound, long acyl-chain-specific 3-hydroxyacyl-CoA dehydrogenase in mammalian mitochondria.

M El-Fakhri, B Middleton.   

Abstract

L-3-Hydroxyacyl-CoA dehydrogenase was measured in mammalian tissues with long-chain (C16) and short-chain (C4) 3-ketoacyl-CoA substrates. The majority of the activity was mitochondrial. Activity with C16 substrate was enriched in the inner membrane fraction while the matrix showed enrichment of activity with C4 substrate. Gel-filtration in the presence of nonionic and ionic detergents separated two peaks of activity with C16 substrate from liver, heart, kidney and brown adipose tissue mitochondria. The highest molecular weight activity was associated with membrane fragments and accounted for 18-32% of the total activity with C16 substrate. This enzyme showed preference for long-chain substrate, the C16/C4 activity ratio being 6-15 for the different mitochondria studied. The other enzyme had a molecular weight of 71 000 and showed highest activity with C4 substrate (C16/C4 activity ratio of 0.2). The substrate specificity of the membrane-associated enzyme was not altered by extraction with detergent or lipid solvents. The membrane-associated enzyme could be partially purified by treatment with high concentrations of KCl and EDTA, when it showed a molecular weight of 186 000 while retaining its high C16/C4 activity ratio. Protease treatment caused loss of C4 activity from the high-molecular-weight enzyme without affecting its C16 activity. We conclude that an inner membrane-associated, long-chain-specific 3-ketoacyl-CoA dehydrogenase coexists in mitochondria with the better-documented matrix enzyme which shows preference for shorter-chain-length substrates.

Entities:  

Mesh:

Substances:

Year:  1982        PMID: 7150615     DOI: 10.1016/0005-2760(82)90244-2

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  18 in total

1.  Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation.

Authors:  R J Wanders; L IJlst; A H van Gennip; C Jakobs; J P de Jager; L Dorland; F J van Sprang; M Duran
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Measurement of the acyl-CoA intermediates of beta-oxidation by h.p.l.c. with on-line radiochemical and photodiode-array detection. Application to the study of [U-14C]hexadecanoate oxidation by intact rat liver mitochondria.

Authors:  N J Watmough; D M Turnbull; H S Sherratt; K Bartlett
Journal:  Biochem J       Date:  1989-08-15       Impact factor: 3.857

3.  The long-chain 3-hydroxyacyl-CoA dehydrogenase of human liver mitochondria.

Authors:  K Carpenter; B Middleton; R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

4.  Cryo-EM structure of human mitochondrial trifunctional protein.

Authors:  Kai Liang; Ningning Li; Xiao Wang; Jianye Dai; Pulan Liu; Chu Wang; Xiao-Wei Chen; Ning Gao; Junyu Xiao
Journal:  Proc Natl Acad Sci U S A       Date:  2018-06-18       Impact factor: 11.205

5.  Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders.

Authors:  J J Shen; D Matern; D S Millington; S Hillman; M D Feezor; M J Bennett; M Qumsiyeh; S G Kahler; Y T Chen; J L Van Hove
Journal:  J Inherit Metab Dis       Date:  2000-02       Impact factor: 4.982

6.  Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency.

Authors:  I Schrijver-Wieling; G H van Rens; D Wittebol-Post; J A Smeitink; J P de Jager; H B de Klerk; G H van Lith
Journal:  Br J Ophthalmol       Date:  1997-04       Impact factor: 4.638

7.  Metabolic consequences of methylenecyclopropylglycine poisoning in rats.

Authors:  K Melde; S Jackson; K Bartlett; H S Sherratt; S Ghisla
Journal:  Biochem J       Date:  1991-03-01       Impact factor: 3.857

Review 8.  Disorders of mitochondrial fatty acyl-CoA beta-oxidation.

Authors:  R J Wanders; P Vreken; M E den Boer; F A Wijburg; A H van Gennip; L IJlst
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

9.  Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients.

Authors:  T Kamijo; R J Wanders; J M Saudubray; T Aoyama; A Komiyama; T Hashimoto
Journal:  J Clin Invest       Date:  1994-04       Impact factor: 14.808

10.  Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patient.

Authors:  R Moore; J F Glasgow; M A Bingham; J A Dodge; R J Pollitt; S E Olpin; B Middleton; K Carpenter
Journal:  Eur J Pediatr       Date:  1993-05       Impact factor: 3.183

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.