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Accessing Nature’s diversity through metabolic engineering and synthetic biology [version 1; referees: 2 approved]

Authors :
Jason R. King
Steven Edgar
Kangjian Qiao
Gregory Stephanopoulos
Author Affiliations :
<relatesTo>1</relatesTo>Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA
Source :
F1000Research. 5:F1000 Faculty Rev-397
Publication Year :
2016
Publisher :
London, UK: F1000 Research Limited, 2016.

Abstract

In this perspective, we highlight recent examples and trends in metabolic engineering and synthetic biology that demonstrate the synthetic potential of enzyme and pathway engineering for natural product discovery. In doing so, we introduce natural paradigms of secondary metabolism whereby simple carbon substrates are combined into complex molecules through “scaffold diversification”, and subsequent “derivatization” of these scaffolds is used to synthesize distinct complex natural products. We provide examples in which modern pathway engineering efforts including combinatorial biosynthesis and biological retrosynthesis can be coupled to directed enzyme evolution and rational enzyme engineering to allow access to the “privileged” chemical space of natural products in industry-proven microbes. Finally, we forecast the potential to produce natural product-like discovery platforms in biological systems that are amenable to single-step discovery, validation, and synthesis for streamlined discovery and production of biologically active agents.

Details

ISSN :
20461402
Volume :
5
Database :
F1000Research
Journal :
F1000Research
Notes :
Editorial Note on the Review Process F1000 Faculty Reviews are commissioned from members of the prestigious F1000 Faculty and are edited as a service to readers. In order to make these reviews as comprehensive and accessible as possible, the referees provide input before publication and only the final, revised version is published. The referees who approved the final version are listed with their names and affiliations but without their reports on earlier versions (any comments will already have been addressed in the published version). The referees who approved this article are: Jon S Thorson, College of Pharmacy, University of Kentuky, Lexington, KY, USA No competing interests were disclosed. Frances H Arnold, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA No competing interests were disclosed., , [version 1; referees: 2 approved]
Publication Type :
Academic Journal
Accession number :
edsfor.10.12688.f1000research.7311.1
Document Type :
review
Full Text :
https://doi.org/10.12688/f1000research.7311.1