Polyketides

Research output: Chapter in book/report/conference proceedingContribution to book/anthologyResearchpeer review

Authors

  • Françoise Schaefers
  • Tobias A.M. Gulder
  • Cyril Bressy
  • Michael Smietana
  • Erica Benedetti
  • Stellios Arseniyadis
  • Markus Kalesse
  • Martin Cordes

Research Organisations

External Research Organisations

  • Technical University of Munich (TUM)
  • Universite d'Aix-Marseille
  • Laboratoire de Chimie et Biochimie et Pharmacologiques et Toxicologique (LCBPT)
  • Queen Mary University of London
  • Helmholtz Centre for Infection Research (HZI)
  • Université Montpellier
View graph of relations

Details

Original languageEnglish
Title of host publicationFrom Biosynthesis to Total Synthesis
Subtitle of host publicationStrategies and Tactics for Natural Products
PublisherWiley-Blackwell
Pages19-129
Number of pages111
ISBN (electronic)9781118754085
ISBN (print)9781118751732
Publication statusPublished - 22 Apr 2016

Abstract

Polyketides are a fascinating class of natural products with highly diverse, often complex structures combined with a likewise impressive breath of strong and selective biological activities. This chapter discusses the logic of biosynthetic polyketide assembly. It focuses on the introduction of the basic mechanisms and concepts of polyketide core structure assembly using a number of well-studied representative examples, thus allowing to compare the biosynthetic versus chemical synthetic strategies to assemble such beautiful small molecules. Despite the structural diversity of polyketide natural products, there are only few different catalytic domains facilitating a small number of basic reactions common to all types of PKSs that are crucial for product biosynthesis. The structural and functional space covered by bioactive small molecules is further expanded by post-PKS functionalization reactions catalyzed by so-called tailoring enzymes. This includes reorganization of the entire PKS core but also subtle changes by group transfer reactions or oxidative transformations.

Keywords

    Biosynthetic pathway, Chemical synthesis, Group transfer reactions, Oxidative transformations, Polyketides

ASJC Scopus subject areas

Cite this

Polyketides. / Schaefers, Françoise; Gulder, Tobias A.M.; Bressy, Cyril et al.
From Biosynthesis to Total Synthesis: Strategies and Tactics for Natural Products. Wiley-Blackwell, 2016. p. 19-129.

Research output: Chapter in book/report/conference proceedingContribution to book/anthologyResearchpeer review

Schaefers, F, Gulder, TAM, Bressy, C, Smietana, M, Benedetti, E, Arseniyadis, S, Kalesse, M & Cordes, M 2016, Polyketides. in From Biosynthesis to Total Synthesis: Strategies and Tactics for Natural Products. Wiley-Blackwell, pp. 19-129. https://doi.org/10.1002/9781118754085.ch2
Schaefers, F., Gulder, T. A. M., Bressy, C., Smietana, M., Benedetti, E., Arseniyadis, S., Kalesse, M., & Cordes, M. (2016). Polyketides. In From Biosynthesis to Total Synthesis: Strategies and Tactics for Natural Products (pp. 19-129). Wiley-Blackwell. https://doi.org/10.1002/9781118754085.ch2
Schaefers F, Gulder TAM, Bressy C, Smietana M, Benedetti E, Arseniyadis S et al. Polyketides. In From Biosynthesis to Total Synthesis: Strategies and Tactics for Natural Products. Wiley-Blackwell. 2016. p. 19-129 Epub 2016 Apr 3. doi: 10.1002/9781118754085.ch2
Schaefers, Françoise ; Gulder, Tobias A.M. ; Bressy, Cyril et al. / Polyketides. From Biosynthesis to Total Synthesis: Strategies and Tactics for Natural Products. Wiley-Blackwell, 2016. pp. 19-129
Download
@inbook{9f43d1ffc1af4a949a3392afc726b3b9,
title = "Polyketides",
abstract = "Polyketides are a fascinating class of natural products with highly diverse, often complex structures combined with a likewise impressive breath of strong and selective biological activities. This chapter discusses the logic of biosynthetic polyketide assembly. It focuses on the introduction of the basic mechanisms and concepts of polyketide core structure assembly using a number of well-studied representative examples, thus allowing to compare the biosynthetic versus chemical synthetic strategies to assemble such beautiful small molecules. Despite the structural diversity of polyketide natural products, there are only few different catalytic domains facilitating a small number of basic reactions common to all types of PKSs that are crucial for product biosynthesis. The structural and functional space covered by bioactive small molecules is further expanded by post-PKS functionalization reactions catalyzed by so-called tailoring enzymes. This includes reorganization of the entire PKS core but also subtle changes by group transfer reactions or oxidative transformations.",
keywords = "Biosynthetic pathway, Chemical synthesis, Group transfer reactions, Oxidative transformations, Polyketides",
author = "Fran{\c c}oise Schaefers and Gulder, {Tobias A.M.} and Cyril Bressy and Michael Smietana and Erica Benedetti and Stellios Arseniyadis and Markus Kalesse and Martin Cordes",
year = "2016",
month = apr,
day = "22",
doi = "10.1002/9781118754085.ch2",
language = "English",
isbn = "9781118751732",
pages = "19--129",
booktitle = "From Biosynthesis to Total Synthesis",
publisher = "Wiley-Blackwell",
address = "United States",

}

Download

TY - CHAP

T1 - Polyketides

AU - Schaefers, Françoise

AU - Gulder, Tobias A.M.

AU - Bressy, Cyril

AU - Smietana, Michael

AU - Benedetti, Erica

AU - Arseniyadis, Stellios

AU - Kalesse, Markus

AU - Cordes, Martin

PY - 2016/4/22

Y1 - 2016/4/22

N2 - Polyketides are a fascinating class of natural products with highly diverse, often complex structures combined with a likewise impressive breath of strong and selective biological activities. This chapter discusses the logic of biosynthetic polyketide assembly. It focuses on the introduction of the basic mechanisms and concepts of polyketide core structure assembly using a number of well-studied representative examples, thus allowing to compare the biosynthetic versus chemical synthetic strategies to assemble such beautiful small molecules. Despite the structural diversity of polyketide natural products, there are only few different catalytic domains facilitating a small number of basic reactions common to all types of PKSs that are crucial for product biosynthesis. The structural and functional space covered by bioactive small molecules is further expanded by post-PKS functionalization reactions catalyzed by so-called tailoring enzymes. This includes reorganization of the entire PKS core but also subtle changes by group transfer reactions or oxidative transformations.

AB - Polyketides are a fascinating class of natural products with highly diverse, often complex structures combined with a likewise impressive breath of strong and selective biological activities. This chapter discusses the logic of biosynthetic polyketide assembly. It focuses on the introduction of the basic mechanisms and concepts of polyketide core structure assembly using a number of well-studied representative examples, thus allowing to compare the biosynthetic versus chemical synthetic strategies to assemble such beautiful small molecules. Despite the structural diversity of polyketide natural products, there are only few different catalytic domains facilitating a small number of basic reactions common to all types of PKSs that are crucial for product biosynthesis. The structural and functional space covered by bioactive small molecules is further expanded by post-PKS functionalization reactions catalyzed by so-called tailoring enzymes. This includes reorganization of the entire PKS core but also subtle changes by group transfer reactions or oxidative transformations.

KW - Biosynthetic pathway

KW - Chemical synthesis

KW - Group transfer reactions

KW - Oxidative transformations

KW - Polyketides

UR - http://www.scopus.com/inward/record.url?scp=85026566193&partnerID=8YFLogxK

U2 - 10.1002/9781118754085.ch2

DO - 10.1002/9781118754085.ch2

M3 - Contribution to book/anthology

AN - SCOPUS:85026566193

SN - 9781118751732

SP - 19

EP - 129

BT - From Biosynthesis to Total Synthesis

PB - Wiley-Blackwell

ER -

By the same author(s)