Combinatorial biosynthesis of 'unnatural' natural products: the polyketide example
- PMID: 9383437
- DOI: 10.1016/1074-5521(95)90214-7
Combinatorial biosynthesis of 'unnatural' natural products: the polyketide example
Abstract
Multi-enzyme systems, such as those involved in the biosynthesis of polyketides, typically catalyze several distinct reactions that are combined in different ways to generate diverse natural products. The variability available in such systems has not been fully harnessed from nature. It may therefore be possible to create 'unnatural' natural products, which may be as structurally diverse and medicinally valuable as existing natural products, using combinatorial biosynthesis.
Similar articles
-
Generation of polyketide libraries via combinatorial biosynthesis.Trends Biotechnol. 1996 Sep;14(9):335-41. doi: 10.1016/0167-7799(96)10046-9. Trends Biotechnol. 1996. PMID: 8818287
-
Engineered intermodular and intramodular polyketide synthase fusions.Chem Biol. 1997 Sep;4(9):667-74. doi: 10.1016/s1074-5521(97)90222-2. Chem Biol. 1997. PMID: 9331407
-
Molecular recognition of diketide substrates by a beta-ketoacyl-acyl carrier protein synthase domain within a bimodular polyketide synthase.Chem Biol. 1997 Oct;4(10):757-66. doi: 10.1016/s1074-5521(97)90314-8. Chem Biol. 1997. PMID: 9375254
-
Combinatorial biosynthesis of antimicrobials and other natural products.Curr Opin Microbiol. 2001 Oct;4(5):526-34. doi: 10.1016/s1369-5274(00)00246-0. Curr Opin Microbiol. 2001. PMID: 11587928 Review.
-
Combinatorial approaches to polyketide biosynthesis.Curr Opin Chem Biol. 1997 Aug;1(2):162-8. doi: 10.1016/s1367-5931(97)80005-1. Curr Opin Chem Biol. 1997. PMID: 9734993 Review.
Cited by
-
Engineering the acyltransferase substrate specificity of assembly line polyketide synthases.J R Soc Interface. 2013 May 29;10(85):20130297. doi: 10.1098/rsif.2013.0297. Print 2013 Aug 6. J R Soc Interface. 2013. PMID: 23720536 Free PMC article. Review.
-
Combinatorial Enzymatic Synthesis of Unnatural Long-Chain β-Branch Pyrones by a Highly Promiscuous Enzyme.ACS Omega. 2019 Dec 5;4(25):21078-21082. doi: 10.1021/acsomega.9b02473. eCollection 2019 Dec 17. ACS Omega. 2019. PMID: 31867500 Free PMC article.
-
Cloning and heterologous expression of the entire gene clusters for PD 116740 from Streptomyces strain WP 4669 and tetrangulol and tetrangomycin from Streptomyces rimosus NRRL 3016.J Bacteriol. 1997 Jan;179(2):470-6. doi: 10.1128/jb.179.2.470-476.1997. J Bacteriol. 1997. PMID: 8990300 Free PMC article.
-
A modular and synthetic biosynthesis platform for de novo production of diverse halogenated tryptophan-derived molecules.Nat Commun. 2024 Apr 12;15(1):3188. doi: 10.1038/s41467-024-47387-1. Nat Commun. 2024. PMID: 38609402 Free PMC article.
-
Design, synthesis, and evaluation of potent bryostatin analogs that modulate PKC translocation selectivity.Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):6721-6. doi: 10.1073/pnas.1015270108. Epub 2011 Mar 17. Proc Natl Acad Sci U S A. 2011. PMID: 21415363 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources