Evidence map›Paper›PMID 39865260›Full record

ArticleMicrobial cell factories2025

Ribosome pausing in amylase producing Bacillus subtilis during long fermentation.

Yaozu Han, Biwen Wang, Alberto Agnolin, Gaurav Dugar, Frans van der Kloet, Christopher Sauer, Paul Igor Costea, Max Fabian Felle, Mathis Appelbaum, Leendert W Hamoen

Abstract read
In one paragraph

Article in Microbial cell factories, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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

10 authors.

Yaozu HanSwammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands.
Biwen WangSwammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands.
Alberto AgnolinSwammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands.
Gaurav DugarSwammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands.
Frans van der KloetSwammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands.
Christopher SauerWhite Biotechnology Research, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein, 67056, Germany.
Paul Igor CosteaWhite Biotechnology Research, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein, 67056, Germany.
Max Fabian FelleWhite Biotechnology Research, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein, 67056, Germany.
Mathis AppelbaumWhite Biotechnology Research, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein, 67056, Germany.
Leendert W HamoenSwammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands. l.w.hamoen@uva.nl.

Funding

EMBO fellowship ALTF 936European Commission MCSA-IF 749510
6 · The paper itself

Abstract

backgroundRibosome pausing slows down translation and can affect protein synthesis. Improving translation efficiency can therefore be of commercial value. In this study, we investigated whether ribosome pausing occurs during production of the α-amylase AmyM by the industrial production organism Bacillus subtilis under repeated batch fermentation conditions.

resultsWe began by assessing our ribosome profiling procedure using the antibiotic mupirocin that blocks translation at isoleucine codons. After achieving single codon resolution for ribosome pausing, we determined the genome wide ribosome pausing sites for B. subtilis at 16 h and 64 h growth under batch fermentation. For the highly expressed α-amylase gene amyM several strong ribosome pausing sites were detected, which remained during the long fermentation despite changes in nutrient availability. These pause sites were neither related to proline or rare codons, nor to secondary protein structures. When surveying the genome, an interesting finding was the presence of strong ribosome pausing sites in several toxins genes. These potential ribosome stall sites may prevent inadvertent activity in the cytosol by means of delayed translation.

conclusionsExpression of the α-amylase gene amyM in B. subtilis is accompanied by several ribosome pausing events. Since these sites can neither be predicted based on codon specificity nor on secondary protein structures, we speculate that secondary mRNA structures are responsible for these translation pausing sites. The detailed information of ribosome pausing sites in amyM provide novel information that can be used in future codon optimization studies aimed at improving the production of this amylase by B. subtilis.

Indexed as

alpha-AmylasesAmylasesBacillus subtilisFermentationRibosomesBacterial ProteinsCodonProtein BiosynthesisRNA, Messengeralpha-AmylasesAmylasesBacterial ProteinsCodonRNA, MessengerAmylaseBacillus subtilisProtein secretionRibosome pausingRibosome profiling

Identifiers

PMID39865260
PMCPMC11770953

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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.