Dictionary:
val·in·o·my·cin (văl'ə-nō-mī'sĭn)
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| 5min Related Video: valinomycin |
| Medical Dictionary: val·in·o·my·cin |
An antibiotic produced by the actinomycete Streptomyces fulvissimus, that increases the transport of potassium across cell membranes.
| Veterinary Dictionary: valinomycin |
Ionophore consisting of a cyclic trimer of tetrapeptides. Specifically transports potassium ions across cell membranes. Inhibitor of oxidative phosphorylation due to its action in antagonizing the proton motive force.
| Wikipedia: Valinomycin |
| Valinomycin | |
|---|---|
| Identifiers | |
| CAS number | [] |
| Properties | |
| Molecular formula | C54H90N6O18 |
| Molar mass | 1111.32 |
| Appearance | White solid |
| Melting point |
172°C -177 °C |
| Solubility | Methanol, Ethanol, Ethyl acetate, Petrol-ether, Dichloromethane |
| λmax | 220 nm |
| Hazards | |
| Main hazards | Neurotoxicant |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
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Valinomycin is a dodecadepsipeptide, that is, it is made of twelve alternating amino acids and esters to form a macrocyclic molecule.
Valinomycin is obtained from the cells of several Streptomyces strains, one of them "S. tsusimaensis".
It is a member of the group of natural neutral ionophores because it doesn't have a residual charge. It consists of enantiomeres D- and L-Valine, D-Hydroxyvaleric acid and L-Lactic acid. Structures are alternated bound via amide and ester bridges. Valinomycin is highly selective for potassium ions over sodium ions within the cell membrane.[1] It functions as a potassium-specific transporter and facilitates the movement of potassium ions through lipid membranes "down" an electrochemical potential gradient.[2] The stability constant K for the potassium-valinomycin complex is 106 and for the sodium-valinomycin complex only 10. This difference is important for maintaining the selectivity of valinomycin for the transport of potassium ions (and not sodium ions) in biological systems.
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Note these salient features and implications of the chemical structure: The 12 carbonyl groups are essential for the binding of metal ions, and also for solvation in polar solvent. The isopropyl groups and methyl groups are responsible for solvation in nonpolar solvents. [3] Along with its shape and size this molecular duality is the main reason for its binding properties. For polar solvents valinomycin will mainly expose the carbonyls to the solvent and in nonpolar solvents the iso-propyl groups are located predominantly on the exterior of the molecule. This conformation changes when valinomycin is bound to a potassium ion. The molecule is "locked" into a conformation with the isopropyl groups on the exterior. It is not actually locked into configuration because the size of the molecule makes it highly flexible, but the potassium ion gives some degree of coordination to the macromolecule.
Valinomycin acts as a non metallic isoforming agent in Potassium selective electrode.[4][5]
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