Literature DB >> 22744619

The generation of "unnatural" products: synthetic biology meets synthetic chemistry.

Rebecca J M Goss1, Sreejith Shankar, Antoine Abou Fayad.   

Abstract

Natural product analogue generation is important, providing tools for chemical biology, enabling structure activity relationship determination and insight into the way in which natural products interact with their target biomolecules. The generation of analogues is also often necessary in order to improve bioavailability and to fine tune compounds' activity. This review provides an overview of the catalogue of approaches available for accessing series of analogues. Over the last few years there have been major advances in genome sequencing and the development of tools for biosynthetic pathway engineering; it is therefore becoming increasingly easy to combine molecular biology and synthetic organic chemistry in order to enable expeditious access to series of natural products. This review outlines the various ways of combining biology and chemistry that have been applied to analogue generation, drawing upon a series of examples to illustrate each approach.

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Year:  2012        PMID: 22744619     DOI: 10.1039/c2np00001f

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  25 in total

1.  Assembly and clustering of natural antibiotics guides target identification.

Authors:  Chad W Johnston; Michael A Skinnider; Chris A Dejong; Philip N Rees; Gregory M Chen; Chelsea G Walker; Shawn French; Eric D Brown; János Bérdy; Dennis Y Liu; Nathan A Magarvey
Journal:  Nat Chem Biol       Date:  2016-02-01       Impact factor: 15.040

2.  Designed biosynthesis of 36-methyl-FK506 by polyketide precursor pathway engineering.

Authors:  Anna Lechner; Micheal C Wilson; Yeon Hee Ban; Jae-Yeon Hwang; Yeo Joon Yoon; Bradley S Moore
Journal:  ACS Synth Biol       Date:  2012-11-05       Impact factor: 5.110

3.  Structural basis of functional group activation by sulfotransferases in complex metabolic pathways.

Authors:  Jennifer Gehret McCarthy; Eli B Eisman; Sarang Kulkarni; Lena Gerwick; William H Gerwick; Peter Wipf; David H Sherman; Janet L Smith
Journal:  ACS Chem Biol       Date:  2012-09-26       Impact factor: 5.100

4.  Use of a biosynthetic intermediate to explore the chemical diversity of pseudo-natural fungal polyketides.

Authors:  Teigo Asai; Kento Tsukada; Satomi Ise; Naoki Shirata; Makoto Hashimoto; Isao Fujii; Katsuya Gomi; Kosuke Nakagawara; Eiichi N Kodama; Yoshiteru Oshima
Journal:  Nat Chem       Date:  2015-08-03       Impact factor: 24.427

5.  Starter unit flexibility for engineered product synthesis by the nonreducing polyketide synthase PksA.

Authors:  Callie R Huitt-Roehl; Eric A Hill; Martina M Adams; Anna L Vagstad; Jesse W Li; Craig A Townsend
Journal:  ACS Chem Biol       Date:  2015-03-10       Impact factor: 5.100

6.  Bacillus sp.: A Remarkable Source of Bioactive Lipopeptides.

Authors:  A Théatre; A C R Hoste; A Rigolet; I Benneceur; M Bechet; M Ongena; M Deleu; P Jacques
Journal:  Adv Biochem Eng Biotechnol       Date:  2022       Impact factor: 2.635

7.  Late-Stage Diversification: A Motivating Force in Organic Synthesis.

Authors:  Kelly E Kim; Alexia N Kim; Carter J McCormick; Brian M Stoltz
Journal:  J Am Chem Soc       Date:  2021-10-06       Impact factor: 16.383

8.  Precursor-Directed Generation of Amidine Containing Ammosamide Analogs: Ammosamides E-P.

Authors:  Ende Pan; Nathaniel W Oswald; Aaron G Legako; Janie M Life; Bruce A Posner; John B Macmillan
Journal:  Chem Sci       Date:  2013-01       Impact factor: 9.825

Review 9.  Recent advances in combinatorial biosynthesis for drug discovery.

Authors:  Huihua Sun; Zihe Liu; Huimin Zhao; Ee Lui Ang
Journal:  Drug Des Devel Ther       Date:  2015-02-12       Impact factor: 4.162

Review 10.  The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research.

Authors:  James B McAlpine; Shao-Nong Chen; Andrei Kutateladze; John B MacMillan; Giovanni Appendino; Andersson Barison; Mehdi A Beniddir; Maique W Biavatti; Stefan Bluml; Asmaa Boufridi; Mark S Butler; Robert J Capon; Young H Choi; David Coppage; Phillip Crews; Michael T Crimmins; Marie Csete; Pradeep Dewapriya; Joseph M Egan; Mary J Garson; Grégory Genta-Jouve; William H Gerwick; Harald Gross; Mary Kay Harper; Precilia Hermanto; James M Hook; Luke Hunter; Damien Jeannerat; Nai-Yun Ji; Tyler A Johnson; David G I Kingston; Hiroyuki Koshino; Hsiau-Wei Lee; Guy Lewin; Jie Li; Roger G Linington; Miaomiao Liu; Kerry L McPhail; Tadeusz F Molinski; Bradley S Moore; Joo-Won Nam; Ram P Neupane; Matthias Niemitz; Jean-Marc Nuzillard; Nicholas H Oberlies; Fernanda M M Ocampos; Guohui Pan; Ronald J Quinn; D Sai Reddy; Jean-Hugues Renault; José Rivera-Chávez; Wolfgang Robien; Carla M Saunders; Thomas J Schmidt; Christoph Seger; Ben Shen; Christoph Steinbeck; Hermann Stuppner; Sonja Sturm; Orazio Taglialatela-Scafati; Dean J Tantillo; Robert Verpoorte; Bin-Gui Wang; Craig M Williams; Philip G Williams; Julien Wist; Jian-Min Yue; Chen Zhang; Zhengren Xu; Charlotte Simmler; David C Lankin; Jonathan Bisson; Guido F Pauli
Journal:  Nat Prod Rep       Date:  2018-07-13       Impact factor: 13.423

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