Evidence map›Paper›PMID 39801078›Full record

ArticleACS synthetic biology2025

Construction and Characterization of MoClo-Compatible Vectors for Modular Protein Expression in

Jochem R Nielsen, Michael J Lewis, Wei E Huang

Abstract read
In one paragraph

Article in ACS synthetic biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Jochem R NielsenDepartment of Engineering Science, University of Oxford, Oxford OX1 3PJ, U.K.
Michael J LewisDepartment of Engineering Science, University of Oxford, Oxford OX1 3PJ, U.K.
Wei E HuangDepartment of Engineering Science, University of Oxford, Oxford OX1 3PJ, U.K.ORCID 0000-0003-1302-6528

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cloning methods are fundamental to synthetic biology research. The capability to generate custom DNA constructs exhibiting predictable protein expression levels is crucial to the engineering of biology. Golden Gate cloning, a modular cloning (MoClo) technique, enables rapid and reliable one-pot assembly of genetic parts. In this study, we expand on the existing MoClo toolkits by constructing and characterizing compatible low- (p15A) and medium-copy (pBR322) destination vectors. Together with existing high-copy vectors, these backbones enable a protein expression range covering a 500-fold difference in normalized fluorescence output. We further characterize the expression- and burden profiles of each vector and demonstrate their use for the optimization of growth-coupled enzyme expression. The optimal expression of

Indexed as

Cloning, MolecularEscherichia coliGenetic VectorsAlcohol DehydrogenasePlasmidsSynthetic BiologyAlcohol Dehydrogenasecopy numberdestination vectorsGFP expressiongolden gate assemblygrowth-coupled selectionMoCloorigin of replicationplasmidplasmid burden

Identifiers

PMID39801078
PMCPMC11852211

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.