logo
ResearchBunny Logo
Accelerating the discovery of alkyl halide-derived natural products using halide depletion

Biology

Accelerating the discovery of alkyl halide-derived natural products using halide depletion

N. R. Glasser, D. Cui, et al.

Discover a groundbreaking workflow in microbial natural product discovery, as presented by Nathaniel R. Glasser, Dongtao Cui, Douglas D. Risser, C. Denise Okafor, and Emily P. Balskus. This research unveils the innovative targeting of alkyl halide-derived natural products and the novel enzymatic reactions that yield chlorinated glycolipids from *Nostoc punctiforme*. Get ready to dive into the biosynthetic logic that is transforming the search for natural compounds!

00:00
00:00
Playback language: English
Abstract
Microbial natural product discovery is often laborious. This paper introduces a novel workflow targeting alkyl halide-derived natural products by depleting halide anions from microbial growth media. Comparing metabolomes of bacteria grown in halide-replete and -deficient media led to the discovery of nostochlorosides, products of an orphan halogenase-encoding gene cluster from *Nostoc punctiforme*. These chlorinated glycolipids, featuring the rare sugar gulose, are polymerized via an unprecedented enzymatic etherification reaction. This highlights using biosynthetic logic to streamline natural product discovery.
Publisher
Nature Chemistry
Published On
Feb 12, 2024
Authors
Nathaniel R. Glasser, Dongtao Cui, Douglas D. Risser, C. Denise Okafor, Emily P. Balskus
Tags
microbial natural products
alkyl halides
nostochlorosides
halogenase
glycolipids
biosynthetic logic
enzyme reactions
Listen, Learn & Level Up
Over 10,000 hours of research content in 25+ fields, available in 12+ languages.
No more digging through PDFs, just hit play and absorb the world's latest research in your language, on your time.
listen to research audio papers with researchbunny