Evidence map›Paper›PMID 38715841›Full record

ArticleAnalytical science advances2022

Time-resolved multiparameter analytics on a cell-free production platform for acyl-CoA precursors.

Dominic Maehler, Sandra Hoefgen, Ute Münchberg, Oliver J Schmitz, Julia Rautschek, Ying Huang, Erik Freier, Vito Valiante

Abstract read
In one paragraph

Article in Analytical science advances, 2022. 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

8 authors.

Dominic MaehlerCARS Microscopy Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V. Dortmund Germany.
Sandra HoefgenBiobricks of Microbial Natural Product Syntheses Leibniz Institute for Natural Product Research and Infections Biology - Hans Knöll Institute Jena Germany.
Ute MünchbergCARS Microscopy Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V. Dortmund Germany.
Oliver J SchmitzApplied Analytical Chemistry, Faculty of Chemistry University of Duisburg-Essen Essen Germany.
Julia RautschekBiobricks of Microbial Natural Product Syntheses Leibniz Institute for Natural Product Research and Infections Biology - Hans Knöll Institute Jena Germany.
Ying HuangBiobricks of Microbial Natural Product Syntheses Leibniz Institute for Natural Product Research and Infections Biology - Hans Knöll Institute Jena Germany.
Erik FreierCARS Microscopy Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V. Dortmund Germany.
Vito ValianteBiobricks of Microbial Natural Product Syntheses Leibniz Institute for Natural Product Research and Infections Biology - Hans Knöll Institute Jena Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-free biosynthesis is emerging as a very attractive alternative for the production of market-relevant molecules. The free combination of enzymes, regardless of where they are isolated from, raises the possibility to build more efficient synthetic routes but at the same time leads to higher complexity regarding the analysis of the different enzymatic steps. Here we present an analytical method for the real-time analysis of acyl-CoA blocks forming and consuming during multi-step catalyses. We focused on malonyl-Coenzyme A and acetyl-CoA, which are the most used acyl-CoA units for carbon chain elongations. By employing capillary electrophoresis, we could detect the decrease of educts and the formation of products in a time-resolved fashion.

Indexed as

acyl‐CoAcapillary electrophoresiscatalysiscell‐free synthesisCoA ligases

Identifiers

PMID38715841
PMCPMC10989585

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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.