Evidence map›Paper›PMID 42645554›Full record

ArticleApplied microbiology and biotechnology2026

Efficient biotechnological production of N-(Hydroxycinnamoyl)tyramines by utilizing plant-derived enzymes in a bench-scale bioreactor with in situ product precipitation.

Israa Abuobida Mohamed, Qais Al-Khawlani, Raika Milde, Niels Valentin Heise, Martin Dippe, Mohamed Nagia, Ludger A Wessjohann, Markus Pietzsch, Bodo Moritz

Erratum issuedAbstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

5 · Who and what money

Authors and funding

9 authors.

Israa Abuobida MohamedInstitute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Weinbergweg 22, 06120, Halle (Saale), Germany.ORCID http://orcid.org/0009-0009-1559-3252
Qais Al-KhawlaniInstitute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Weinbergweg 22, 06120, Halle (Saale), Germany.ORCID http://orcid.org/0009-0005-1452-7203
Raika MildeInstitute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Weinbergweg 22, 06120, Halle (Saale), Germany.ORCID http://orcid.org/0000-0003-0630-8105
Niels Valentin HeiseInstitute of Chemistry, Martin-Luther-University Halle-Wittenberg, Kurt-Mothes-Straße 2, 06120, Halle, Germany.ORCID http://orcid.org/0000-0002-6540-6357
Martin DippeLeibniz-Institute of Plant Biochemistry, Department of Bioorganic Chemistry, Weinberg 3, 06120, Halle, Germany.ORCID http://orcid.org/0000-0001-7123-7812
Mohamed NagiaInstitute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Weinbergweg 22, 06120, Halle (Saale), Germany.ORCID http://orcid.org/0000-0002-7280-5153
Ludger A WessjohannLeibniz-Institute of Plant Biochemistry, Department of Bioorganic Chemistry, Weinberg 3, 06120, Halle, Germany.ORCID http://orcid.org/0000-0003-2060-8235
Markus PietzschInstitute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Weinbergweg 22, 06120, Halle (Saale), Germany.ORCID http://orcid.org/0000-0001-6266-9621
Bodo MoritzInstitute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Weinbergweg 22, 06120, Halle (Saale), Germany. bodo.moritz@pharmazie.uni-halle.de.ORCID https://orcid.org/0009-0005-9339-3409

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficient recovery of plant polyphenolic bioactives is facing technological challenges of low concentrations and complex mixtures starting from plant tissue. In the search of alternatives, we developed a high-yield biotechnological production process for hydroxycinnamic acid-tyramine conjugates in Escherichia coli by converting soluble substrates into insoluble products. A recombinant plant-enzyme cascade was established by co-expression of Arabidopsis thaliana 4-coumarate:CoA ligase and Solanum tuberosum hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase. We overcame initial enzymatic limitations by developing a temperature adapted and sequentially phased bioprocess on a 1 L reactor scale. With 5 mM/h substrate supply rate we achieved 31.9 g/L (102 mM) of feruloyltyramine (FerT), 14.4 g/L (50.7 mM) coumaroyltyramine, and 14.6 g/L (46.5 mM) isoferuloyltyramine with a space time yield of 1.75 g *L

Indexed as

BioreactorsBiotechnologyCoumaric AcidsTyramineArabidopsisCoenzyme A LigasesEscherichia coliRecombinant ProteinsTemperature4-coumarate-CoA ligaseCoenzyme A LigasesCoumaric AcidsferuloyltyramineRecombinant ProteinsTyramineCoumaroyltyramineFeruloyltyramineHigh cell density fermentationHydroxycinnamic acid amideMetabolic engineeringPhenyl propanoic acidsProduct recovery

Identifiers

PMID42645554
PMCPMC13518753

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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.