[HTML][HTML] Recent highlights of biosynthetic studies on marine natural products

JA Moghaddam, T Jautzus, M Alanjary… - Organic & …, 2021 - pubs.rsc.org
Marine bacteria are excellent yet often underexplored sources of structurally unique
bioactive natural products. In this review we cover the diversity of marine bacterial …

Structural basis of the nonribosomal codes for nonproteinogenic amino acid selective adenylation enzymes in the biosynthesis of natural products

F Kudo, A Miyanaga, T Eguchi - Journal of Industrial …, 2019 - academic.oup.com
Nonproteinogenic amino acids are the unique building blocks of nonribosomal peptides
(NRPs) and hybrid nonribosomal peptide–polyketides (NRP–PKs) and contribute to their …

Gut-inhabiting Clostridia build human GPCR ligands by conjugating neurotransmitters with diet-and human-derived fatty acids

FY Chang, P Siuti, S Laurent, T Williams… - Nature …, 2021 - nature.com
Human physiology is regulated by endogenous signalling compounds, including fatty acid
amides (FAAs), chemical mimics of which are made by bacteria. The molecules produced by …

Expanding the Chemical Diversity of Grisechelins via Heterologous Expression

W Liu, S Zhai, L Zhang, Y Chen, Z Liu… - Journal of Natural …, 2024 - ACS Publications
Thiazole scaffold-based small molecules exhibit a range of biological activities and play
important roles in drug discovery. Based on bioinformatics analysis, a putative biosynthetic …

Deciphering Nature's Intricate Way of N,S-Dimethylating l-Cysteine: Sequential Action of Two Bifunctional Adenylation Domains

S Mori, A Garzan, OV Tsodikov… - Biochemistry, 2017 - ACS Publications
Dimethylation of amino acids consists of an interesting and puzzling series of events that
could be achieved, during nonribosomal peptide biosynthesis, either by a single adenylation …

Natural product bis-intercalator depsipeptides as a new class of payloads for antibody–drug conjugates

AS Ratnayake, L Chang, LN Tumey… - Bioconjugate …, 2018 - ACS Publications
A potent class of DNA-damaging agents, natural product bis-intercalator depsipeptides
(NPBIDs), was evaluated as ultrapotent payloads for use in antibody–drug conjugates …

Using MbtH‐like proteins to alter the substrate profile of a nonribosomal peptide adenylation enzyme

S Mori, KD Green, R Choi, GW Buchko… - …, 2018 - Wiley Online Library
MbtH‐like proteins (MLPs) are required for soluble expression and/or optimal activity of
some adenylation (A) domains of nonribosomal peptide synthetases. Because A domains …

Electrochemically Oxidative Coupling of S‐H/S‐H for S‐S Bond Formation: A Facile Approach to Diacid‐disulfides

XJ Sun, SF Yang, ZT Wang, S Liang, HY Tian… - …, 2020 - Wiley Online Library
A green electrochemical method of preparing diacid‐disulfides has been developed, in
which an S− S bond is formed by electrochemically oxidative coupling of S− H/S− H …

[HTML][HTML] Complete Genome Sequence Analysis of Kribbella sp. CA-293567 and Identification of the Kribbellichelins A & B and Sandramycin Biosynthetic Gene …

M Sánchez-Hidalgo, MJ García, I González… - Microorganisms, 2023 - mdpi.com
Minor genera actinomycetes are considered a promising source of new secondary
metabolites. The strain Kribbella sp. CA-293567 produces sandramycin and kribbellichelins …

Characterization and Engineering of Interrupted Adenylation Domains

TA Lundy - 2020 - uknowledge.uky.edu
Nature has historically served as a prolific source of biologically active molecules produced
by plants, fungi, and bacteria termed natural products (NPs). These NPs often serve as …