Oxidative cyclization in natural product biosynthesis

MC Tang, Y Zou, K Watanabe, CT Walsh… - Chemical …, 2017 - ACS Publications
Oxidative cyclizations are important transformations that occur widely during natural product
biosynthesis. The transformations from acyclic precursors to cyclized products can afford …

Biosynthesis of fungal meroterpenoids

Y Matsuda, I Abe - Natural product reports, 2016 - pubs.rsc.org
Covering: up to September 2015 Meroterpenoids are hybrid natural products that partially
originate from the terpenoid pathway. The meroterpenoids derived from fungi display quite …

Bacterial terpenome

JD Rudolf, TA Alsup, B Xu, Z Li - Natural product reports, 2021 - pubs.rsc.org
Covering: up to mid-2020 Terpenoids, also called isoprenoids, are the largest and most
structurally diverse family of natural products. Found in all domains of life, there are over 80 …

Enzymatic cascade reactions in biosynthesis

CT Walsh, BS Moore - Angewandte Chemie International …, 2019 - Wiley Online Library
Enzyme‐mediated cascade reactions are widespread in biosynthesis. To facilitate
comparison with the mechanistic categorizations of cascade reactions by synthetic chemists …

How the conformational movement of the substrate drives the regioselective C–N bond formation in P450 TleB: insights from molecular dynamics simulations and …

Z Wang, W Diao, P Wu, J Li, Y Fu, Z Guo… - Journal of the …, 2023 - ACS Publications
P450 TleB catalyzes the oxidative cyclization of the dipeptide N-methylvalyl-tryptophanol
into indolactam V through selective intramolecular C–H bond amination at the indole C4 …

Terpene synthases in disguise: enzymology, structure, and opportunities of non-canonical terpene synthases

JD Rudolf, CY Chang - Natural product reports, 2020 - pubs.rsc.org
Covering: up to July 2019 Terpene synthases (TSs) are responsible for generating much of
the structural diversity found in the superfamily of terpenoid natural products. These elegant …

Marine indole alkaloids

N Netz, T Opatz - Marine drugs, 2015 - mdpi.com
Marine indole alkaloids comprise a large and steadily growing group of secondary
metabolites. Their diverse biological activities make many compounds of this class attractive …

S-Adenosylmethionine: more than just a methyl donor

YH Lee, D Ren, B Jeon, H Liu - Natural product reports, 2023 - pubs.rsc.org
Covering: from 2000 up to the very early part of 2023 S-Adenosyl-L-methionine (SAM) is a
naturally occurring trialkyl sulfonium molecule that is typically associated with biological …

Bacterial diterpene biosynthesis

JS Dickschat - Angewandte Chemie International Edition, 2019 - Wiley Online Library
This Minireview summarises recent developments in the biosynthesis of diterpenes by
diterpene synthases in bacteria. It is structured by the class of enzyme involved in the first …

Prenyltransferases as key enzymes in primary and secondary metabolism

J Winkelblech, A Fan, SM Li - Applied microbiology and biotechnology, 2015 - Springer
Attachment of isoprene units to various acceptors by prenylation plays an important role in
primary and secondary metabolism of living organisms. Protein prenylation belongs to …