Literature DB >> 3790097

Hysteretic behaviour of carnitine palmitoyltransferase. The effect of preincubation with malonyl-CoA.

G A Cook, K A Cox.   

Abstract

Continuous assays of carnitine palmitoyltransferase were used to study the hysteretic behaviour of the enzyme. When reactions were started by adding mitochondria to complete reaction mixtures, there was a lag in the assay even in the absence of malonyl-CoA. When mitochondria were preincubated with malonyl-CoA in the absence of palmitoyl-CoA, there was a greater lag period in the assay of carnitine palmitoyltransferase, but this lag was less prominent at 37 degrees C than at 30 degrees C. Preincubation of mitochondria with malonyl-CoA did not change the sensitivity of the enzyme to inhibition by malonyl-CoA.

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Year:  1986        PMID: 3790097      PMCID: PMC1146927          DOI: 10.1042/bj2360917

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  13 in total

1.  Effect of glucagon on hepatic malonyl coenzyme A concentration and on lipid synthesis.

Authors:  G A Cook; R C Nielsen; R A Hawkins; M A Mehlman; M R Lakshmanan; R L Veech
Journal:  J Biol Chem       Date:  1977-06-25       Impact factor: 5.157

2.  Involvement of hysteretic effects in the inhibition of carnitine palmitoyltransferase by malonyl-CoA.

Authors:  G A Cook
Journal:  Biochem J       Date:  1984-12-15       Impact factor: 3.857

3.  Carnitine acyltransferase activities in rat liver and heart measured with palmitoyl-CoA and octanoyl-CoA. Latency, effects of K+, bivalent metal ions and malonyl-CoA.

Authors:  E D Saggerson
Journal:  Biochem J       Date:  1982-02-15       Impact factor: 3.857

4.  Differences in the sensitivity of carnitine palmitoyltransferase to inhibition by malonyl-CoA are due to differences in Ki values.

Authors:  G A Cook
Journal:  J Biol Chem       Date:  1984-10-10       Impact factor: 5.157

5.  Effects of the mode of addition of acyl-CoA on the initial rate of formation of acylcarnitine in the presence of carnitine by intact rat liver mitochondria in vitro.

Authors:  V A Zammit
Journal:  Biochem J       Date:  1985-07-01       Impact factor: 3.857

6.  Differential inhibition of ketogenesis by malonyl-CoA in mitochondria from fed and starved rats.

Authors:  G A Cook; D A Otto; N W Cornell
Journal:  Biochem J       Date:  1980-12-15       Impact factor: 3.857

7.  Evaluation of malonyl-CoA in the regulation of long-chain fatty acid oxidation in the liver. Evidence for an unidentified regulatory component of the system.

Authors:  J A Ontko; M L Johns
Journal:  Biochem J       Date:  1980-12-15       Impact factor: 3.857

8.  Sensitivity of carnitine acyltransferase I to malonly-CoA inhibition in isolated rat liver mitochondria is quantitatively related to hepatic malonyl-CoA concentration in vivo.

Authors:  I N Robinson; V A Zammit
Journal:  Biochem J       Date:  1982-07-15       Impact factor: 3.857

9.  Time-dependence of inhibition of carnitine palmitoyltransferase I by malonyl-CoA in mitochondria isolated from livers of fed or starved rats. Evidence for transition of the enzyme between states of low and high affinity for malonyl-CoA.

Authors:  V A Zammit
Journal:  Biochem J       Date:  1984-03-01       Impact factor: 3.857

10.  Ketogenesis and malonyl coenzyme A content of isolated rat hepatocytes.

Authors:  G A Cook; M T King; R L Veech
Journal:  J Biol Chem       Date:  1978-04-25       Impact factor: 5.157

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  3 in total

1.  L-carnitine acyltransferase in intact peroxisomes is inhibited by malonyl-CoA.

Authors:  J P Derrick; R R Ramsay
Journal:  Biochem J       Date:  1989-09-15       Impact factor: 3.857

2.  Fatty acid chain elongation in palmitate-perfused working rat heart: mitochondrial acetyl-CoA is the source of two-carbon units for chain elongation.

Authors:  Janos Kerner; Paul E Minkler; Edward J Lesnefsky; Charles L Hoppel
Journal:  J Biol Chem       Date:  2014-02-20       Impact factor: 5.157

3.  Studies on the activation in vitro of carnitine palmitoyltransferase I in liver mitochondria from normal, diabetic and glucagon-treated rats.

Authors:  B D Grantham; V A Zammit
Journal:  Biochem J       Date:  1987-04-01       Impact factor: 3.857

  3 in total

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