Evidence map›Paper›PMID 40679465›Full record

ArticleJournal of industrial microbiology & biotechnology2024

Engineering Streptomyces coelicolor for heterologous expression of the thiopeptide GE2270A-A cautionary tale.

Francesco Del Carratore, Erik K R Hanko, Kamila Schmidt, Oksana Bilyk, Suhui Ye Huang, Marianna Iorio, Mercedes Pérez-Bonilla, Rosario Pérez-Redondo, Michelle Rudden, Emmanuele Severi and 12 more

Abstract read
In one paragraph

Article in Journal of industrial microbiology & biotechnology, 2024. 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. Synthetic and systems biotechnology · 2026
    Review
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

22 authors.

Francesco Del CarratoreDepartment of Biochemistry, Cell, and Systems Biology, Institute of Integrative, Systems and Molecular Biology, University of Liverpool, Liverpool L69 3BX, UK.ORCID 0000-0003-1647-7818
Erik K R HankoManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0002-2850-7773
Kamila SchmidtManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0002-7763-1500
Oksana BilykManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0002-8159-8088
Suhui Ye HuangManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0002-4466-4242
Marianna IorioNAICONS Srl, Milan, Italy.ORCID 0000-0001-8669-5875
Mercedes Pérez-BonillaFundación MEDINA, Parque Tecnológico Ciencias de la Salud, Avda. Conocimiento 34, 18016 Granada, Spain.
Rosario Pérez-RedondoInstituto de Biotecnología de León, INBIOTEC, León, Spain.ORCID 0000-0002-8782-8796
Michelle RuddenDepartment of Biology and York Biomedical Research Institute (YBRI), University of York, Wentworth Way, York YO10 5DD, UK.
Emmanuele SeveriDepartment of Biology and York Biomedical Research Institute (YBRI), University of York, Wentworth Way, York YO10 5DD, UK.ORCID 0000-0001-9750-5539
Arianna TocchettiNAICONS Srl, Milan, Italy.ORCID 0000-0001-7004-7582
Margherita SosioNAICONS Srl, Milan, Italy.
Emily J JohnsonComputational Biology Facility, Liverpool Shared Research Facilities, Faculty of Health and Life Sciences, University of Liverpool, Liverpool L69 7ZB, UK.
Timothy KirkwoodManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0002-6485-0608
Dominic R WhittallManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0001-6176-1872
Alkisti ManousakiManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.
Olga GenilloudFundación MEDINA, Parque Tecnológico Ciencias de la Salud, Avda. Conocimiento 34, 18016 Granada, Spain.
Antonio Rodríguez-GarcíaÁrea de Microbiología, Departamento de Biología Molecular, Facultad de Ciencias Biológicas y Ambientales, Universidad de León, León, Spain.ORCID 0000-0001-8118-9762
Gavin H ThomasFundación Centro de Servicios y Promoción Forestal y de su Industria de Castilla y León, Cesefor. Sede INBIOTEC, Avda. Real 1, 24006 León, España.
Stefano DonadioNAICONS Srl, Milan, Italy.ORCID 0000-0002-2121-8979
Rainer BreitlingManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.
Eriko TakanoManchester Institute of Biotechnology, School of Chemistry, Faculty of Science and Engineering, University of Manchester, Manchester M1 7DN, UK.ORCID 0000-0002-6791-3256

Funding

Biotechnology and Biological Sciences Research Council BB/X012573/1Engineering and Physical Sciences Research Council BB/M017702/1Horizon 2020 720793UK Research and Innovation NE/T010959/1
6 · The paper itself

Abstract

The thiopeptide GE2270A is a clinically relevant, ribosomally synthesised, and post-translationally modified peptide naturally produced by Planobispora rosea. Due to the genetically intractable nature of P. rosea, heterologous expression is considered a possible route to yield improvement. In this study, we focused on improving GE2270A production through heterologous expression of the biosynthetic gene cluster (BGC) in the model organism Streptomyces coelicolor M1146. A statistically significant yield improvement was obtained in the S. coelicolor system through the data-driven rational engineering of the BGC, including the introduction of additional copies of key biosynthetic and regulatory genes. However, despite our best efforts, the highest production level observed in the strains generated in this study is 12× lower than published titres achieved in the natural producer and 50× lower than published titres obtained using Nonomuraea ATCC 39727 as expression host. These results suggest that, while using the most genetically amenable strain as host can be the right choice when exploring different BGC designs, the choice of the most suitable host has a major effect on the achievable yield and should be carefully considered. The analysis of the multiomics data obtained in this study suggests an important role of PbtX in GE2270A biosynthesis and provides insights into the differences in production metabolic profiles between the different strains. One Sentence Summary: Data-driven rational engineering of Streptomyces coelicolor for heterologous production of the thiopeptide antibiotic GE2270A resulted in increased production but encountered unexpected challenges compared to production in the natural producer or the alternative host Nonomuraea ATCC 39727.

Indexed as

Metabolic EngineeringPeptides, CyclicStreptomyces coelicolorBacterial ProteinsBiosynthetic PathwaysGene ExpressionMultigene FamilyBacterial ProteinsPeptides, CyclicGE2270AMetabolic engineeringStreptomyces coelicolorSynthetic biologyThiopeptide

Identifiers

PMID40679465
PMCPMC12309360

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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.