New developments in RiPP discovery, enzymology and engineering

M Montalbán-López, TA Scott, S Ramesh… - Natural product …, 2021 - pubs.rsc.org
Covering: up to June 2020 Ribosomally-synthesized and post-translationally modified
peptides (RiPPs) are a large group of natural products. A community-driven review in 2013 …

[PDF][PDF] Engineering lanthipeptides by introducing a large variety of RiPP modifications to obtain new-to-nature bioactive peptides

Y Fu, Y Xu, F Ruijne, OP Kuipers - FEMS Microbiology Reviews, 2023 - academic.oup.com
Natural bioactive peptide discovery is a challenging and time-consuming process. However,
advances in synthetic biology are providing promising new avenues in peptide engineering …

Parallel lives of symbionts and hosts: chemical mutualism in marine animals

M Morita, EW Schmidt - Natural product reports, 2018 - pubs.rsc.org
Covering: up to 2018 Symbiotic microbes interact with animals, often by producing natural
products (specialized metabolites; secondary metabolites) that exert a biological role. A …

The biochemistry and structural biology of cyanobactin pathways: enabling combinatorial biosynthesis

W Gu, SH Dong, S Sarkar, SK Nair, EW Schmidt - Methods in enzymology, 2018 - Elsevier
Cyanobactin biosynthetic enzymes have exceptional versatility in the synthesis of natural
and unnatural products. Cyanobactins are ribosomally synthesized and posttranslationally …

Mechanisms and evolution of diversity-generating RiPP biosynthesis

T Le, WA van der Donk - Trends in Chemistry, 2021 - cell.com
This review focuses on the prochlorosin and cyanobactin biosynthetic pathways, unusual
examples of pathways in cyanobacteria that appear to be diversity generating. In the case of …

Chemoenzymatic Late‐Stage Modifications Enable Downstream Click‐Mediated Fluorescent Tagging of Peptides

A Colombano, L Dalponte, S Dall'Angelo… - Angewandte Chemie …, 2023 - Wiley Online Library
Aromatic prenyltransferases from cyanobactin biosynthetic pathways catalyse the
chemoselective and regioselective intramolecular transfer of prenyl/geranyl groups from …

Expanding the chemical space of synthetic cyclic peptides using a promiscuous macrocyclase from prenylagaramide biosynthesis

S Sarkar, W Gu, EW Schmidt - ACS catalysis, 2020 - ACS Publications
Cyclic peptides are ubiquitous drug candidates, placing macrocyclization reactions at the
apex of drug development. PatG and related dual-action proteases from cyanobactin …

Promiscuity of Omphalotin A Biosynthetic Enzymes Allows de novo Production of Non‐Natural Multiply Backbone N‐Methylated Peptide Macrocycles in Yeast

E Matabaro, L Witte, F Gherlone, E Vogt… - …, 2024 - Wiley Online Library
Multiple backbone N‐methylation and macrocyclization improve the proteolytic stability and
oral availability of therapeutic peptides. Chemical synthesis of such peptides is challenging …

Possible Functional Roles of Patellamides in the Ascidian-Prochloron Symbiosis

P Baur, M Kühl, P Comba, L Behrendt - Marine Drugs, 2022 - mdpi.com
Patellamides are highly bioactive compounds found along with other cyanobactins in the
symbiosis between didemnid ascidians and the enigmatic cyanobacterium Prochloron. The …

Biochemical characterization of a cyanobactin arginine-N-prenylase from the autumnalamide biosynthetic pathway

C Clemente, N Johnson, X Ouyang, RV Popin… - Chemical …, 2022 - pubs.rsc.org
Cyanobactins are linear and cyclic post-translationally modified peptides. Here we show that
the prenyl-D-Arg-containing autumnalamide A is a member of the cyanobactin family …