Biosynthesis of the antitumor chromomycin A3 in Streptomyces griseus: analysis of the gene cluster and rational design of novel chromomycin analogs
- PMID: 15112992
- DOI: 10.1016/j.chembiol.2003.12.011
Biosynthesis of the antitumor chromomycin A3 in Streptomyces griseus: analysis of the gene cluster and rational design of novel chromomycin analogs
Abstract
The biosynthetic gene cluster of the aureolic acid type antitumor drug chromomycin A3 from S. griseus subsp. griseus has been identified and characterized. It spans 43 kb and contains 36 genes involved in polyketide biosynthesis and modification, deoxysugar biosynthesis and sugar transfer, pathway regulation and resistance. The organization of the cluster clearly differs from that of the closely related mithramycin. Involvement of the cluster in chromomycin A3 biosynthesis was demonstrated by disrupting the cmmWI gene encoding a polyketide reductase involved in side chain reduction. Three novel chromomycin derivatives were obtained, named chromomycin SK, chromomycin SA, and chromomycin SDK, which show antitumor activity and differ with respect to their 3-side chains. A pathway for the biosynthesis of chromomycin A3 and its deoxysugars is proposed.
Comment in
-
Aureolic acids: similar antibiotics with different biosynthetic gene clusters.Chem Biol. 2004 Jan;11(1):8-10. doi: 10.1016/j.chembiol.2004.01.006. Chem Biol. 2004. PMID: 15112986
Similar articles
-
Deoxysugar transfer during chromomycin A3 biosynthesis in Streptomyces griseus subsp. griseus: new derivatives with antitumor activity.Appl Environ Microbiol. 2006 Jan;72(1):167-77. doi: 10.1128/AEM.72.1.167-177.2006. Appl Environ Microbiol. 2006. PMID: 16391039 Free PMC article.
-
Tailoring modification of deoxysugars during biosynthesis of the antitumour drug chromomycin A by Streptomyces griseus ssp. griseus.Mol Microbiol. 2004 Aug;53(3):903-15. doi: 10.1111/j.1365-2958.2004.04166.x. Mol Microbiol. 2004. PMID: 15255901
-
Aureolic acids: similar antibiotics with different biosynthetic gene clusters.Chem Biol. 2004 Jan;11(1):8-10. doi: 10.1016/j.chembiol.2004.01.006. Chem Biol. 2004. PMID: 15112986
-
The aureolic acid family of antitumor compounds: structure, mode of action, biosynthesis, and novel derivatives.Appl Microbiol Biotechnol. 2006 Nov;73(1):1-14. doi: 10.1007/s00253-006-0511-6. Epub 2006 Sep 30. Appl Microbiol Biotechnol. 2006. PMID: 17013601 Review.
-
Candicidin biosynthesis in Streptomyces griseus.Appl Microbiol Biotechnol. 2003 Feb;60(6):633-42. doi: 10.1007/s00253-002-1163-9. Epub 2002 Dec 18. Appl Microbiol Biotechnol. 2003. PMID: 12664141 Review.
Cited by
-
Manipulation of two regulatory genes for efficient production of chromomycins in Streptomyces reseiscleroticus.J Biol Eng. 2018 Jun 7;12:9. doi: 10.1186/s13036-018-0103-x. eCollection 2018. J Biol Eng. 2018. PMID: 29977332 Free PMC article.
-
Metathramycin, a new bioactive aureolic acid discovered by heterologous expression of a metagenome derived biosynthetic pathway.RSC Chem Biol. 2021 Feb 2;2(2):556-567. doi: 10.1039/d0cb00228c. eCollection 2021 Apr 1. RSC Chem Biol. 2021. PMID: 34458799 Free PMC article.
-
Antitumor compounds from Streptomyces sp. KML-2, isolated from Khewra salt mines, Pakistan.Biol Res. 2015 Oct 14;48:58. doi: 10.1186/s40659-015-0046-3. Biol Res. 2015. PMID: 26466995 Free PMC article.
-
Chromomycin SA analogs from a marine-derived Streptomyces sp.Bioorg Med Chem. 2011 Sep 1;19(17):5183-9. doi: 10.1016/j.bmc.2011.07.013. Epub 2011 Jul 20. Bioorg Med Chem. 2011. PMID: 21807523 Free PMC article.
-
Molecular insights on the biosynthesis of antitumour compounds by actinomycetes.Microb Biotechnol. 2011 Mar;4(2):144-64. doi: 10.1111/j.1751-7915.2010.00231.x. Epub 2010 Nov 18. Microb Biotechnol. 2011. PMID: 21342461 Free PMC article. Review.
Publication types
MeSH terms
Substances
Associated data
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources