نتایج جستجو برای: long chain acyl coa synthetase

تعداد نتایج: 1084410  

Journal: :The Journal of biological chemistry 1970
S Smith S Abraham

Homogeneous preparations of fatty acid synthetase from mammary glands of lactating rats were used to prepare an antiserum and a y-globulin fraction was isolated from the antiserum. The antiserum and the y-globulin fraction were shown to be specific against the fatty acid synthetase multienzyme complex. Addition of the y-globulin to homogenate fractions of lactating rat mammary glsnds, resulted ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1978
W D Nunn R W Simons

A new locus (fadL) that is required for the utilization of long-chain fatty acids has been mapped and partially characterized in an Escherichia coli mutant. The fadL locus has been mapped at 50 min on the chromosome. A mutant bearing a defect in this locus cannot utilize long-chain fatty acids as a sole carbon source. Derivatives of this mutant that can grow on decanoate (termed fadR) are capab...

Journal: :The Journal of clinical investigation 1987
R J Wanders C W van Roermund M J van Wijland R B Schutgens J Heikoop H van den Bosch A W Schram J M Tager

The peroxisomal oxidation of the long chain fatty acid palmitate (C16:0) and the very long chain fatty acids lignocerate (C24:0) and cerotate (C26:0) was studied in freshly prepared homogenates of cultured skin fibroblasts from control individuals and patients with peroxisomal disorders. The peroxisomal oxidation of the fatty acids is almost completely dependent on the addition of ATP, coenzyme...

Journal: :genetics in the 3rd millennium 0
مرال توپوکو meral topcu prof of pediatrics, hacettepe university children’s hospital, department of pediatric neurology

metabolic myopathies are genetically inherited disorders of muscle energy production that result in skeletal muscle dysfunction. they are a large group of diseases with diverse inborn errors of metabolism, in particular muscle energy production, and including disorders of glycogen (lysosomal and non-lysosomal glycogenoses), lipid (disorders of fatty acid b-oxidation, primary carnitine deficienc...

Journal: :The Biochemical journal 1987
R Hovik H Osmundsen

Rates of peroxisomal beta-oxidation were measured as fatty acyl-CoA-dependent NAD+ reduction, by using solubilized peroxisomal fractions isolated from livers of rats treated with clofibrate. Medium- to long-chain saturated fatty acyl-CoA esters as well as long-chain polyunsaturated fatty acyl-CoA esters were used. Peroxisomal beta-oxidation shows optimal specificity towards long-chain polyunsat...

Journal: :The Biochemical journal 1970
P B Garland D W Yates B A Haddock

1. Deca-2,4,6,8-tetraenoic acid is a substrate for both ATP-specific (EC 6.2.1.2 or 3) and GTP-specific (EC 6.2.1.-) acyl-CoA synthetases of rat liver mitochondria. The enzymic synthesis of decatetraenoyl-CoA results in new spectral characteristics. The difference spectrum for the acyl-CoA minus free acid has a maximum at 376nm with epsilon(mM) 34. Isosbestic points are at 345nm and 440nm. 2. T...

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