Related Experiment Video
Updated: Aug 21, 2026

Quantification of Coenzyme A in Cells and Tissues
Published on: September 27, 2019
C75 activates malonyl-CoA sensitive and insensitive components of the CPT system
Carine Nicot1, Laura Napal, Joana Relat
1Department of Biochemistry and Molecular Biology, School of Pharmacy University of Barcelona, E-08028 Barcelona, Spain.
Abstract:
Carnitine palmitoyltransferase I (CPT-I) and II (CPT-II) enzymes are components of the carnitine palmitoyltransferase shuttle system which allows entry of long-chain fatty acids into the mitochondrial matrix for subsequent oxidation. This system is tightly regulated by malonyl-CoA levels since this metabolite is a strong reversible inhibitor of the CPT-I enzyme. There are two distinct CPT-I isotypes (CPT-Ialpha and CPT-Ibeta), that exhibit different sensitivity to malonyl-CoA inhibition. Because of its ability to inhibit fatty acid synthase, C75 is able to increase malonyl-CoA intracellular levels. Paradoxically it also activates long-chain fatty acid oxidation. To identify the exact target of C75 within the CPT system, we expressed individually the different components of the system in the yeast Pichia pastoris. We show here that C75 acts on recombinant CPT-Ialpha, but also on the other CPT-I isotype (CPT-Ibeta) and the malonyl-CoA insensitive component of the CPT system, CPT-II.
Related Concept Videos
Overview of Fatty Acid Metabolism
Fatty acids are catabolized in a process called beta-oxidation, which takes place in the matrix of the mitochondria and converts their fatty acid chains into two-carbon units of acetyl groups. The acetyl...
cAMP-dependent Protein Kinase Pathways
Lipid Catabolism
Calmodulin-dependent Signaling
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives
GPCRs Regulate Adenylyl Cylase Activity
Two...
