Bilirubin
Cytochrome C
Gastric Mucin
HCG
FSH
UTI
PMSG
Aprotinin
Asparaginase
Beta Glucanase
Bromelain
Chymotrypsin
Kallikrein
Lysozyme
Pancreatin
Papain
Pepsin
Streptokinase
Trypsin
Urokinase
Coenzyme A
Coenzyme A Trilithium
Coenzyme Q10
Beta Glucans
Chitosan
Chondroitin Sulfate
Dextran
Dextran Sulfate Sodium
Glucosamine HCl
Heparin Sodium
Heparinoid
Hyaluronic Acid
Rosemary Extract
Sodium Cholate
Bilirubin
Cytochrome C
Gastric Mucin
HCG
FSH
UTI
PMSG
Aprotinin
Asparaginase
Beta Glucanase
Bromelain
Chymotrypsin
Kallikrein
Lysozyme
Pancreatin
Papain
Pepsin
Streptokinase
Trypsin
Urokinase
Coenzyme A
Coenzyme A Trilithium
Coenzyme Q10
Beta Glucans
Chitosan
Chondroitin Sulfate
Dextran
Dextran Sulfate Sodium
Glucosamine HCl
Heparin Sodium
Heparinoid
Hyaluronic Acid
Rosemary Extract
Sodium Cholate
Jiagen Biotechnologies
Coenzymes

Coenzyme A (Free Acid)

CAS No:85-61-0
EINECS No:201-616-2
Synonyms:CoA, Co-A, CoASH, Co-A-SH, SH-CoA, HS-CoA, Coenzyme A hydrate, Coenzymum A, Coenzyme A (free acid) from yeast, Acetyl CoA, Coenzyme for transacetylation

Product Summary

Coenzyme A (CoA) is a vital metabolic cofactor found in all living cells, functioning primarily as an acyl group carrier. It plays a central role in the metabolism of carbohydrates, fats, and proteins by facilitating the synthesis and oxidation of fatty acids and the oxidation of pyruvate in the citric acid cycle. Coenzyme A is often referred to as Acetyl CoA when it is transferring an acetyl group. CoA is typically produced through microbial fermentation (e.g., engineered E. coli or Corynebacterium glutamicum).

  • Formula: C21H36N7O16P3S·xH2O
  • Formula Molecular Weight: 767.53 (as anhydrous free acid)
  • Water: Not more than 5%
  • Purity: Not less than 85%
  • Assay (anhydrous basis): Not less than 300 Units/mg

Function

Coenzyme A acts as a carrier of acyl groups (R-CO–), forming thioester derivatives (e.g., acetyl-CoA, succinyl-CoA). These activated intermediates participate in enzymatic reactions across various metabolic pathways. The key enzymes using Coenzyme A are: acetyl-CoA synthetase, fatty acid synthase, pyruvate dehydrogenase complex, and acyl-CoA dehydrogenases.

Mechanism of Action

The reactive thiol (-SH) group of Coenzyme A forms high-energy thioester bonds with carboxylic acids. This facilitates enzymatic group transfers in:
  • The citric acid cycle
  • Fatty acid β-oxidation
  • Amino acid metabolism
  • Ketogenesis and cholesterol synthesis

Applications in Scientific Research

  • Used to study metabolic flux, enzyme kinetics, and acyl-group transfer reactions.
  • Applied in synthetic biology and metabolic reprogramming to drive energy production or biosynthesis of targeted compounds.
  • Radiolabeled or isotopically enriched Coenzyme A (e.g., [¹⁴C]Acetyl-CoA) helps trace biochemical pathways.
  • CoA-dependent enzymes are key to industrial biosynthesis of fine chemicals, pharmaceuticals, and biofuels.
  • CoA-binding pockets serve as targets in antibacterial and antiparasitic drug development (e.g., inhibitors of CoA biosynthesis in Plasmodium falciparum or Mycobacterium tuberculosis).

Packaging & Storage

  • Coenzyme A is available as white or slightly yellow powder
  • Soluble in water and saline, insoluble in ethanol, ether and acetone. Appearance of solution should be clear and slightly opalescent.
  • Store at -20°C (lyophilized powder); –80°C in aliquots with antioxidants (e.g., DTT) to prevent oxidation (solution).

References

  1. Leonardi R, et al. 2005: Coenzyme A: back in action, Prog Lipid Res 44(2-3):125-53.
  2. Gout I. 2018: Coenzyme A, protein CoAlation and redox regulation in mammalian cells, Biochem Soc Trans. 46(3):721-8.
  3. Theodoulou FL. 2014: Coenzyme A and its derivatives: Renaissance of a textbook classic, Biochem Soc Trans. 42(4):1025-32.
  4. Barritt SA. 2024: Coenzyme A biosynthesis: mechanisms of regulation, function and disease, Nat Metab 6(6):1008-1023.
  5. Mignani L, et al. 2021: Coenzyme A biochemistry: from neurodevelopment to neurodegeneration, Brain Sci. 11(8):1031.
  6. Dobrzyn P. 2022: CoA in Health and Disease, Int J Mol Sci. 23(8):4371.
  7. Mishra PK, Drueckhammer DG. 2000: Coenzyme A analogues and derivatives: Synthesis and applications as mechanistic probes of Coenzyme A ester-utilizing enzymes, Chem Rev 100(9):3283-3310.
  8. Hegg EL, et al. 2004: Unraveling the Structure and Mechanism of Acetyl-Coenzyme A Synthase, Acc Chem Res. 37(10):775-83.
  9. Sanichar R, Vederas JC. 2017: One step transformation of Coenzyme A into analogues by transamidation, Organ Lett 19(8):1939-2198.
  10. Hu Y, et al. 2017: CoA-dependent coordination polymer as a novel electrochemical sensing platform for sensitive detection of hydrogen peroxide in biological environments, J Electroanal Chem 801(15):306-14.
  11. Wang Q, et al. 2016: Signal-on CoA-dependent electrochemical biosensor for highly sensitive and label-free detection of Citrate synthase activity, Talanta 161:583-591.
  12. van der Sluis R, Erasmus E. 2016: Xenobiotic/medium chain fatty acid: CoA ligase – a critical review on its role in fatty acid metabolism and the detoxification of benzoic acid and aspirin, Expert Opin Drug Metab Toxicol. 12(10):1169-79.

Jiagen Biotechnologies supplies quality Coenzyme A (Free Acid) of various specifications.
Contact us at sales@jiagen.ca to place an order.

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