[HTML][HTML] Macrocyclization reactions: the importance of conformational, configurational, and template-induced preorganization

V Marti-Centelles, MD Pandey, MI Burguete… - Chemical …, 2015 - ACS Publications
Macrocyclic structures are common synthetic targets in drug discovery,(1, 2) and therefore,
interest in their study is continuously increasing in this field.(3, 4) A classic example is …

PKS and NRPS release mechanisms

L Du, L Lou - Natural product reports, 2010 - pubs.rsc.org
Covering: up to September 2009 This review covers the recent literature on the release
mechanisms for polyketides and nonribosomal peptides produced by microorganisms. The …

[HTML][HTML] Developing fungal heterologous expression platforms to explore and improve the production of natural products from fungal biodiversity

X Meng, Y Fang, M Ding, Y Zhang, K Jia, Z Li… - Biotechnology …, 2022 - Elsevier
Natural products from fungi represent an important source of biologically active metabolites
notably for therapeutic agent development. Genome sequencing revealed that the number …

Navigating the fungal polyketide chemical space: from genes to molecules

YH Chooi, Y Tang - The Journal of organic chemistry, 2012 - ACS Publications
The iterative type I polyketide synthases (IPKSs) are central to the biosynthesis of an
enormously diverse array of natural products in fungi. These natural products, known as …

Polyketide synthase and non-ribosomal peptide synthetase thioesterase selectivity: logic gate or a victim of fate?

ME Horsman, TPA Hari, CN Boddy - Natural product reports, 2016 - pubs.rsc.org
Covering: 1999 to 2014 Type 1, α/β hydrolase-like thioesterase (TE) domains are essential
offloading enzymes, releasing covalently bound products from fatty acid, polyketide, and non …

Recent advancements in the biosynthetic mechanisms for polyketide‐derived mycotoxins

J Huffman, R Gerber, L Du - Biopolymers, 2010 - Wiley Online Library
Polyketides (PKs) are a large group of natural products produced by microorganisms and
plants. They are biopolymers of acetate and other short carboxylates and are biosynthesized …

LovG: the thioesterase required for dihydromonacolin L release and lovastatin nonaketide synthase turnover in lovastatin biosynthesis.

W Xu, YH Chooi, JW Choi, S Li… - Angewandte …, 2013 - search.ebscohost.com
The article discusses research on the development of a biocatalytic process for monacolin J
acid conversion into simvastatin acid. It acknowledges necessity of identifying a complete …

Saccharomyces cerevisiae as host for the recombinant production of polyketides and nonribosomal peptides

A Tippelt, M Nett - Microbial Cell Factories, 2021 - Springer
As a robust, fast growing and genetically tractable organism, the budding yeast
Saccharomyces cerevisiae is one of the most widely used hosts in biotechnology. Its …

High-titer production of olivetolic acid and analogs in engineered fungal host using a nonplant biosynthetic pathway

IC Okorafor, M Chen, Y Tang - ACS synthetic biology, 2021 - ACS Publications
The microbial synthesis of cannabinoids and related molecules requires access to the
intermediate olivetolic acid (OA). Whereas plant enzymes have been explored for E. coli and …

Insights into radicicol biosynthesis via heterologous synthesis of intermediates and analogs

JC Vederas - Journal of Biological Chemistry, 2010 - ASBMB
Resorcylic acid lactones are fungal polyketides that display diverse biological activities, with
the potent Hsp90 inhibitor radicicol being an important representative member. Two fungal …