Literature DB >> 17912378

Total synthesis approaches to natural product derivatives based on the combination of chemical synthesis and metabolic engineering.

Andreas Kirschning1, Florian Taft, Tobias Knobloch.   

Abstract

Secondary metabolites are an extremely diverse and important group of natural products with industrial and biomedical implications. Advances in metabolic engineering of both native and heterologous secondary metabolite producing organisms have allowed the directed synthesis of desired novel products by exploiting their biosynthetic potentials. Metabolic engineering utilises knowledge of cellular metabolism to alter biosynthetic pathways. An important technique that combines chemical synthesis with metabolic engineering is mutasynthesis (mutational biosynthesis; MBS), which advanced from precursor-directed biosynthesis (PDB). Both techniques are based on the cellular uptake of modified biosynthetic intermediates and their incorporation into complex secondary metabolites. Mutasynthesis utilises genetically engineered organisms in conjunction with feeding of chemically modified intermediates. From a synthetic chemist's point of view the concept of mutasynthesis is highly attractive, as the method combines chemical expertise with Nature's synthetic machinery and thus can be exploited to rapidly create small libraries of secondary metabolites. However, in each case, the method has to be critically compared with semi- and total synthesis in terms of practicability and efficiency. Recent developments in metabolic engineering promise to further broaden the scope of outsourcing chemically demanding steps to biological systems.

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Year:  2007        PMID: 17912378     DOI: 10.1039/b709549j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  13 in total

Review 1.  Natural products as chemical probes.

Authors:  Erin E Carlson
Journal:  ACS Chem Biol       Date:  2010-07-16       Impact factor: 5.100

2.  Engineered biosynthesis of antiprotealide and other unnatural salinosporamide proteasome inhibitors.

Authors:  Ryan P McGlinchey; Markus Nett; Alessandra S Eustáquio; Ratnakar N Asolkar; William Fenical; Bradley S Moore
Journal:  J Am Chem Soc       Date:  2008-05-31       Impact factor: 15.419

3.  Precursor directed biosynthesis of an orthogonally functional erythromycin analogue: selectivity in the ribosome macrolide binding pocket.

Authors:  Colin J B Harvey; Joseph D Puglisi; Vijay S Pande; David E Cane; Chaitan Khosla
Journal:  J Am Chem Soc       Date:  2012-07-11       Impact factor: 15.419

4.  Identification of a Thioesterase Bottleneck in the Pikromycin Pathway through Full-Module Processing of Unnatural Pentaketides.

Authors:  Douglas A Hansen; Aaron A Koch; David H Sherman
Journal:  J Am Chem Soc       Date:  2017-09-19       Impact factor: 15.419

5.  Broad substrate specificity of the amide synthase in S. hygroscopicus--new 20-membered macrolactones derived from geldanamycin.

Authors:  Simone Eichner; Timo Eichner; Heinz G Floss; Jörg Fohrer; Edgar Hofer; Florenz Sasse; Carsten Zeilinger; Andreas Kirschning
Journal:  J Am Chem Soc       Date:  2012-01-10       Impact factor: 15.419

6.  Exploiting enzymatic promiscuity to engineer a focused library of highly selective antifungal and antiproliferative aureothin analogues.

Authors:  Martina Werneburg; Benjamin Busch; Jing He; Martin E A Richter; Longkuan Xiang; Bradley S Moore; Martin Roth; Hans-Martin Dahse; Christian Hertweck
Journal:  J Am Chem Soc       Date:  2010-08-04       Impact factor: 15.419

7.  Functional characterization of the cyclomarin/cyclomarazine prenyltransferase CymD directs the biosynthesis of unnatural cyclic peptides.

Authors:  Andrew W Schultz; Chad A Lewis; Michael R Luzung; Phil S Baran; Bradley S Moore
Journal:  J Nat Prod       Date:  2010-03-26       Impact factor: 4.050

8.  Unprecedented deoxygenation at C-7 of the ansamitocin core during mutasynthetic biotransformations.

Authors:  Tobias Knobloch; Gerald Dräger; Wera Collisi; Florenz Sasse; Andreas Kirschning
Journal:  Beilstein J Org Chem       Date:  2012-06-11       Impact factor: 2.883

9.  Preparation of new alkyne-modified ansamitocins by mutasynthesis.

Authors:  Kirsten Harmrolfs; Lena Mancuso; Binia Drung; Florenz Sasse; Andreas Kirschning
Journal:  Beilstein J Org Chem       Date:  2014-03-03       Impact factor: 2.883

10.  Commentary: Toward a new focus in antibiotic and drug discovery from the Streptomyces arsenal.

Authors:  Dipesh Dhakal; Jae Kyung Sohng
Journal:  Front Microbiol       Date:  2015-07-16       Impact factor: 5.640

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