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Thiopeptide Antibiotics: Retrospective and Recent Advances

Overview
Journal Mar Drugs
Publisher MDPI
Specialties Biology
Pharmacology
Date 2014 Jan 22
PMID 24445304
Citations 68
Authors
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Abstract

Thiopeptides, or thiazolyl peptides, are a relatively new family of antibiotics that already counts with more than one hundred different entities. Although they are mainly isolated from soil bacteria, during the last decade, new members have been isolated from marine samples. Far from being limited to their innate antibacterial activity, thiopeptides have been found to possess a wide range of biological properties, including anticancer, antiplasmodial, immunosuppressive, etc. In spite of their ribosomal origin, these highly posttranslationally processed peptides have posed a fascinating synthetic challenge, prompting the development of various methodologies and strategies. Regardless of their limited solubility, intensive investigations are bringing thiopeptide derivatives closer to the clinic, where they are likely to show their veritable therapeutic potential.

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References
1.
Favret M, Paschal J, Elzey T, Boeck L . Biosynthesis of thiopeptide antibiotic A10255: incorporation of isotopically-labeled precursors. J Antibiot (Tokyo). 1992; 45(9):1499-511. DOI: 10.7164/antibiotics.45.1499. View

2.
Kelly W, Pan L, Li C . Thiostrepton biosynthesis: prototype for a new family of bacteriocins. J Am Chem Soc. 2009; 131(12):4327-34. DOI: 10.1021/ja807890a. View

3.
Wieland Brown L, Acker M, Clardy J, Walsh C, Fischbach M . Thirteen posttranslational modifications convert a 14-residue peptide into the antibiotic thiocillin. Proc Natl Acad Sci U S A. 2009; 106(8):2549-53. PMC: 2650375. DOI: 10.1073/pnas.0900008106. View

4.
LaMarche M, Leeds J, Amaral K, Brewer J, Bushell S, Dewhurst J . Antibacterial optimization of 4-aminothiazolyl analogues of the natural product GE2270 A: identification of the cycloalkylcarboxylic acids. J Med Chem. 2011; 54(23):8099-109. DOI: 10.1021/jm200938f. View

5.
JAMBOR W, STEINBERG B, SUYDAM L . Thiostrepton, a new antibiotic. III. In vivo studies. Antibiot Annu. 1955; 3:562-5. View