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Open Access Articles- Top Results for Polyene antimycotic

Polyene antimycotic

Polyene antimycotics, sometimes referred to as polyene antibiotics, are a class of antimicrobial polyene compounds that target fungi.[1] These polyene antimycotics are typically obtained from some species of Streptomyces bacteria. The polyenes bind to ergosterol in the fungal cell membrane and thus weakens it, causing leakage of K+ and Na+ ions, which may contribute to fungal cell death. Amphotericin B, nystatin, and natamycin are examples of polyene antimycotics. They are a subgroup of macrolides.[2]

Structures

Their chemical structures feature a large ring of atoms (in essence, a cyclic ester ring) containing multiple conjugated carbon-carbon double bonds (hence polyene) on one side of the ring and multiple hydroxyl groups bonded to the other side of the ring. Their structures also often have a d-mycosamine (a type of amino-glycoside) group bonded to the molecule.[3] The series of conjugated double bonds typically absorbs strongly in the ultraviolet-visible region of the electromagnetic spectrum, often resulting in the polyene antibiotics having a yellow color.

File:Amphotericin B new.svg
Chemical structure of Amphotericin B. Amphotericin B is an example of a yellow polyene antimycotic agent. Note the alternating double and single bonds in the center and the mycosamine group in the bottom-right corner.
File:Nystatin.svg
Chemical structure of Nystatin.
File:Natamycin.svg
Chemical structure of Natamycin, sometimes called pimaricin.

Biosynthesis

The natural route to synthesis includes polyketide synthase components.[4]

Other examples of polyenes

References

  1. ^ NCBI Bookshelf (1996). "Polyene Antifungal Drugs". The University of Texas Medical Branch at Galveston. Retrieved 29 January 2010. 
  2. ^ Hamilton-Miller (1973). "Chemistry and Biology of the Polyene Macrolide Antibiotics" (PDF). Bacteriological Reviews (American Society for Microbiology) 37 (2): 166–196. PMC 413810. PMID 4578757. 
  3. ^ Solution NMR structure of five representative glycosylated polyene macrolide antibiotics
  4. ^ Khan N, Rawlings B, Caffrey P (Jan 26, 2011). "A labile point in mutant amphotericin polyketide synthases". Biotechnol Lett. 33 (6): 1121–6. PMID 21267757. doi:10.1007/s10529-011-0538-3. 


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