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valinomycin

 
Dictionary: val·in·o·my·cin   (văl'ə-nō-mī'sĭn) pronunciation

n.
An antibiotic, C54H90N6O18, produced by the actinomycete B Streptomyces fulvissimus, that increases the transport of potassium across cell membranes.

[VALIN(E) + -MYCIN.]


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Medical Dictionary: val·in·o·my·cin
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(văl'ə-nō-mī'sĭn)
n.

An antibiotic produced by the actinomycete Streptomyces fulvissimus, that increases the transport of potassium across cell membranes.

Veterinary Dictionary: valinomycin
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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
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Valinomycin
Identifiers
CAS number [2001-95-8]
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

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.

Contents

Structure

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.

Application

Valinomycin acts as a non metallic isoforming agent in Potassium selective electrode.[4][5]

References

  1. ^ Rose Lars and Jenkins ATA (2007). "The effect of the ionophore valinomycin on biomimetic solid supported lipid DPPTE/EPC membranes". Bioelectrochem. 70 (2): 387–393. doi:10.1016/j.bioelechem.2006.05.009.  Entrez Pubmed 16875886
  2. ^ Cammann K (1985). "Ion-selective bulk membranes as models". Top. Curr. Chem. 128: 219–258. 
  3. ^ Thompson M and Krull UJ (1982). "The electroanalytical response of the bilayer lipid membrane to valinomycin: membrane cholesterol content". Anal. Chim. Acta 141: 33–47. doi:10.1016/S0003-2670(01)95308-5. 
  4. ^ Safiulina D, Veksler V, Zharkovsky A and Kaasik A (2006). "Loss of mitochondrial membrane potential is associated with increase in mitochondrial volume: physiological role in neurones". J Cell Physiol 206 (2): 347–353. doi:10.1002/jcp.20476.  Entrez Pubmed 16110491
  5. ^ Potassium ionophore Bulletin

External links


 
 
Learn More
ionophore (biochemistry)
Isabella Helen Karle (American crystallographer)
Isabella Karle

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Copyrights:

Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2009. Published by Houghton Mifflin Company. All rights reserved.  Read more
Medical Dictionary. The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company Read more
Veterinary Dictionary. Saunders Comprehensive Veterinary Dictionary 3rd Edition. Copyright © 2007 by D.C. Blood, V.P. Studdert and C.C. Gay, Elsevier. All rights reserved.  Read more
Wikipedia. This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article "Valinomycin" Read more