Evidence map›Paper›PMID 37488111›Full record

ArticleNature communications2023

A tripartite microbial co-culture system for de novo biosynthesis of diverse plant phenylpropanoids.

Sierra M Brooks, Celeste Marsan, Kevin B Reed, Shuo-Fu Yuan, Dustin-Dat Nguyen, Adit Trivedi, Gokce Altin-Yavuzarslan, Nathan Ballinger, Alshakim Nelson, Hal S Alper

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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  16. Electrocatalytic COSmall science · 2024
    Article
  17. Bioproduction of methylated phenylpropenes and isoeugenol inMetabolic engineering communications · 2024
    Article
  18. Article
  19. Article
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

10 authors.

Sierra M BrooksMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.ORCID 0000-0002-6914-2504
Celeste MarsanMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.
Kevin B ReedMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.
Shuo-Fu YuanInstitute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX, USA.ORCID 0000-0002-5530-8702
Dustin-Dat NguyenInstitute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX, USA.
Adit TrivediMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.
Gokce Altin-YavuzarslanMolecular Engineering and Sciences Institute, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0001-9577-3257
Nathan BallingerDepartment of Chemistry, University of Washington, Box 351700, Seattle, WA, USA.ORCID 0000-0002-9213-529X
Alshakim NelsonMolecular Engineering and Sciences Institute, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0001-8060-8611
Hal S AlperMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA. halper@che.utexas.edu.ORCID 0000-0002-8246-8605

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant-derived phenylpropanoids, in particular phenylpropenes, have diverse industrial applications ranging from flavors and fragrances to polymers and pharmaceuticals. Heterologous biosynthesis of these products has the potential to address low, seasonally dependent yields hindering ease of widespread manufacturing. However, previous efforts have been hindered by the inherent pathway promiscuity and the microbial toxicity of key pathway intermediates. Here, in this study, we establish the propensity of a tripartite microbial co-culture to overcome these limitations and demonstrate to our knowledge the first reported de novo phenylpropene production from simple sugar starting materials. After initially designing the system to accumulate eugenol, the platform modularity and downstream enzyme promiscuity was leveraged to quickly create avenues for hydroxychavicol and chavicol production. The consortia was found to be compatible with Engineered Living Material production platforms that allow for reusable, cold-chain-independent distributed manufacturing. This work lays the foundation for further deployment of modular microbial approaches to produce plant secondary metabolites.

Indexed as

CommercePerfumeCoculture TechniquesKnowledgeMonosaccharidesMonosaccharidesPerfume

Identifiers

PMID37488111
PMCPMC10366228

What OpenQuestion holds

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LicenceCC BY
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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.