Evidence map›Paper›PMID 38216751›Full record

ArticleNature chemistry2024

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

Nathaniel R Glasser, Dongtao Cui, Douglas D Risser, C Denise Okafor, Emily P Balskus

Open access · hybridAbstract read
In one paragraph

Article in Nature chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.8field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Nathaniel R GlasserDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
Dongtao CuiDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.ORCID 0009-0007-5579-8848
Douglas D RisserDepartment of Biology, University of the Pacific, Stockton, CA, USA.ORCID 0000-0003-1981-0049
C Denise OkaforDepartment of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA, USA.
Emily P BalskusDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA. balskus@chemistry.harvard.edu.ORCID 0000-0001-5985-5714
Harvard University · USHoward Hughes Medical Institute · USPennsylvania State University · USUniversity of the Pacific · US

Funding

National Science Foundation (NSF) 1753690National Science Foundation (NSF) 1907240National Science Foundation (NSF) CHE-2003436
6 · The paper itself

Abstract

Even in the genomic era, microbial natural product discovery workflows can be laborious and limited in their ability to target molecules with specific structural features. Here we leverage an understanding of biosynthesis to develop a workflow that targets the discovery of alkyl halide-derived natural products by depleting halide anions, a key biosynthetic substrate for enzymatic halogenation, from microbial growth media. By comparing the metabolomes of bacterial cultures grown in halide-replete and deficient media, we rapidly discovered the nostochlorosides, the products of an orphan halogenase-encoding gene cluster from Nostoc punctiforme ATCC 29133. We further found that these products, a family of unusual chlorinated glycolipids featuring the rare sugar gulose, are polymerized via an unprecedented enzymatic etherification reaction. Together, our results highlight the power of leveraging an understanding of biosynthetic logic to streamline natural product discovery.

Indexed as

Biological ProductsHalogenationBiological Products

Identifiers

PMID38216751
PMCPMC10849952
OpenAlexW4390822007

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.