Evidence map›Paper›PMID 42633465›Full record

ArticleSynthetic biology (Oxford, England)2026

Integration-coupled activation of promoterless combinatorial pathway libraries in

Pawel M Mordaka, James J Williamson, John T Heap

Abstract read
In one paragraph

Article in Synthetic biology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Pawel M MordakaImperial College Centre for Synthetic Biology, Department of Life Sciences, Imperial College London, London SW7 2AZ, United Kingdom.ORCID https://orcid.org/0000-0003-2989-8224
James J WilliamsonSchool of Life Sciences, Biodiscovery Institute, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom.ORCID https://orcid.org/0000-0003-1485-8772
John T HeapImperial College Centre for Synthetic Biology, Department of Life Sciences, Imperial College London, London SW7 2AZ, United Kingdom.ORCID https://orcid.org/0000-0001-9991-5160

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combinatorial DNA design and assembly is an efficient and pragmatic way to obtain high-performing metabolic pathway designs quickly. However, implementation may require organism-specific technical barriers to be overcome. Firstly, suitable expression control parts such as promoters and ribosome-binding sites (RBSs), which provide a suitable range of expression levels, need to be identified or developed. Secondly, these need to be assembled into pathway-encoding combinatorial libraries of sufficient size, quality, and diversity. For organisms with transformation frequencies too low to allow direct transformation of library assembly reactions, such as many

Indexed as

Clostridiumcombinatorial assemblynon-model organismssynthetic regulation

Identifiers

PMID42633465
PMCPMC13499600

What OpenQuestion holds

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Registered trials

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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.