Evidence map›Paper›PMID 40468089›Full record

ArticleApplied microbiology and biotechnology2025

Extracellular peptide production in Escherichia coli by inducible downregulation of lipoprotein Lpp via MicL sRNA.

Martin Gibisch, Pawel Gorecki, Christopher Tauer, Esther Egger, Matthias Müller, Bernd Albrecht, Rainer Hahn, Gerald Striedner, Monika Cserjan-Puschmann

Abstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2025. 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

9 authors.

Martin GibischChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria.
Pawel GoreckiChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria.
Christopher TauerChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria.
Esther EggerChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria.
Matthias MüllerChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria.
Bernd AlbrechtBoehringer-Ingelheim RCV, GmbH & Co KG, Dr.-Boehringer-Gasse 5-11, Vienna, 1120, Austria.
Rainer HahnChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria.
Gerald StriednerChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria.
Monika Cserjan-PuschmannChristian Doppler Laboratory for Production of Next-Level Biopharmaceuticals in 𝐸. 𝐶𝑜𝑙𝑖, Institute of Bioprocess Science and Engineering, BOKU University, Muthgasse 18, 1190, Vienna, Austria. monika.cserjan@boku.ac.at.ORCID http://orcid.org/0000-0002-9811-9709

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite its many benefits, Escherichia coli only poorly secretes recombinant proteins and peptides into the medium. This complicates downstream processing and notably contributes to the production costs of biopharmaceuticals. The permeability of production strains can be increased by deletion of the lpp gene, coding for Braun's lipoprotein Lpp. Consequently, the outer membrane (OM) is destabilized, and periplasmic recombinant proteins/peptides can leak out of the cell into the cultivation medium. However, we observed poor process performance during C-limited fed-batch cultivations in bioreactors when production strains with lpp knockout were cultivated. In this study, we developed an inducible system for in-process Lpp downregulation (knockdown) in E. coli with the goal to facilitate the release of the periplasmic recombinant fusion peptide CASPON-SST into the cultivation medium. By plasmid-based overexpression of MicL sRNA, we were able to efficiently inhibit Lpp synthesis and increase the OM permeability of our production strains. With this approach, we were able to achieve the secretion of 80-100% of all peptide and increased production capacities. The system was further optimized by utilizing different promoter systems to induce peptide and MicL expression separately in order to coordinate them. We report here for the first time the extracellular production of a recombinant peptide by inducible downregulation of Lpp via MicL sRNA during C-limited fed-batch cultivations. By utilizing a flexible system for Lpp knockdown, potential drawbacks of lpp knockout can be counteracted, thus making our approach a valuable tool for the in-process adaptation of OM permeability in production hosts. KEY POINTS: • Lpp can be downregulated on mRNA level by MicL sRNA overexpressed during fed-batch. • Recombinant peptides can leak out of the periplasm when Lpp is downregulated. • Leakiness and outer membrane permeability must be distinguished.

Indexed as

Bacterial Outer Membrane ProteinsEscherichia coliEscherichia coli ProteinsLipoproteinsPeptidesRNA, Small UntranslatedBioreactorsDown-RegulationGene Expression Regulation, BacterialRecombinant ProteinsBacterial Outer Membrane ProteinsEscherichia coli ProteinsLipoproteinsLpp protein, E coliPeptidesRecombinant ProteinsRNA, Small UntranslatedFed-batchKnockdownLeaky strainsOuter membranePeriplasmic peptidesPermeabilitySecretion

Identifiers

PMID40468089
PMCPMC12137417

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.