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Biosynthesis and Pathway Engineering of Antifungal Polyene Macrolides in Actinomycetes

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Specialty Biotechnology
Date 2013 Mar 22
PMID 23515854
Citations 11
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Abstract

Polyene macrolides are a large family of natural products typically produced by soil actinomycetes. Polyene macrolides are usually biosynthesized by modular and large type I polyketide synthases (PKSs), followed by several steps of sequential post-PKS modifications such as region-specific oxidations and glycosylations. Although known as powerful antibiotics containing potent antifungal activities (along with additional activities against parasites, enveloped viruses and prion diseases), their high toxicity toward mammalian cells and poor distribution in tissues have led to the continuous identification and structural modification of polyene macrolides to expand their general uses. Advances in in-depth investigations of the biosynthetic mechanism of polyene macrolides and the genetic manipulations of the polyene biosynthetic pathways provide great opportunities to generate new analogues. Recently, a novel class of polyene antibiotics was discovered (a disaccharide-containing NPP) that displays better pharmacological properties such as improved water-solubility and reduced hemolysis. In this review, we summarize the recent advances in the biosynthesis, pathway engineering, and regulation of polyene antibiotics in actinomycetes.

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References
1.
Nic Lochlainn L, Caffrey P . Phosphomannose isomerase and phosphomannomutase gene disruptions in Streptomyces nodosus: impact on amphotericin biosynthesis and implications for glycosylation engineering. Metab Eng. 2008; 11(1):40-7. DOI: 10.1016/j.ymben.2008.08.007. View

2.
Anton N, Santos-Aberturas J, Mendes M, Guerra S, Martin J, Aparicio J . PimM, a PAS domain positive regulator of pimaricin biosynthesis in Streptomyces natalensis. Microbiology (Reading). 2007; 153(Pt 9):3174-3183. DOI: 10.1099/mic.0.2007/009126-0. View

3.
Lemke A, Kiderlen A, Kayser O . Amphotericin B. Appl Microbiol Biotechnol. 2005; 68(2):151-62. DOI: 10.1007/s00253-005-1955-9. View

4.
Martin J, DEMAIN A . Control of antibiotic biosynthesis. Microbiol Rev. 1980; 44(2):230-51. PMC: 373178. DOI: 10.1128/mr.44.2.230-251.1980. View

5.
Du Y, Chen S, Cheng L, Shen X, Tian Y, Li Y . Identification of a novel Streptomyces chattanoogensis L10 and enhancing its natamycin production by overexpressing positive regulator ScnRII. J Microbiol. 2009; 47(4):506-13. DOI: 10.1007/s12275-009-0014-0. View