Evidence map›Paper›PMID 32170856›Full record

ArticleMicrobiologyOpen2020

Multifunctional SEVA shuttle vectors for actinomycetes and Gram-negative bacteria.

Coral García-Gutiérrez, Tomás Aparicio, Lucía Torres-Sánchez, Esteban Martínez-García, Víctor de Lorenzo, Claudio J Villar, Felipe Lombó

Open access · goldAbstract read
In one paragraph

Article in MicrobiologyOpen, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

16 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The extended mobility of plasmids.Nucleic acids research · 2025
    Review
  5. Review
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  10. Article
  11. Optimized De Novo Eriodictyol Biosynthesis inInternational journal of molecular sciences · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

7 authors at 2 institutions in 1 country.

Coral García-GutiérrezResearch Group BIONUC (Biotechnology of Nutraceuticals and Bioactive Compounds), Departamento de Biología Funcional, Área de Microbiología, Universidad de Oviedo, Oviedo, Spain.
Tomás AparicioSystems Biology Program, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Lucía Torres-SánchezResearch Group BIONUC (Biotechnology of Nutraceuticals and Bioactive Compounds), Departamento de Biología Funcional, Área de Microbiología, Universidad de Oviedo, Oviedo, Spain.ORCID 0000-0001-8486-0005
Esteban Martínez-GarcíaSystems Biology Program, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Víctor de LorenzoSystems Biology Program, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Claudio J VillarResearch Group BIONUC (Biotechnology of Nutraceuticals and Bioactive Compounds), Departamento de Biología Funcional, Área de Microbiología, Universidad de Oviedo, Oviedo, Spain.
Felipe LombóResearch Group BIONUC (Biotechnology of Nutraceuticals and Bioactive Compounds), Departamento de Biología Funcional, Área de Microbiología, Universidad de Oviedo, Oviedo, Spain.ORCID 0000-0002-6680-6723
Universidad de Oviedo · ESCentro Nacional de Biotecnología · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Actinomycetales, such as the genus Streptomyces, are well-known cell factories employed to produce a wide variety of secondary metabolites for industrial use. However, not only is the genetic engineering of Streptomyces more complicated and tedious than other model laboratory species, such as Escherichia coli, there is also a considerable lack of genetic tools, hindering its adoption as a common chassis for synthetic biology. In this work, 23 novel shuttle vectors are presented that follow the canonical SEVA (Standard European Vector Architecture) common architecture with the goal of increasing the genetic toolbox repertoire for Streptomyces and other actinomycetes. The ORI module of these plasmids is composed of the combination of two origins of replication, one for Gram-negative bacteria and the other for Streptomyces, a Gram-positive bacteria. Origins of replication have been included in the collection for integrative, low-copy number, and medium-to-high-copy number vectors for Streptomyces. Also, a new selection marker has been developed that confers resistance to apramycin. The functionality of these plasmids was tested via the heterologous expression of GFP and the heterologous production of the plant flavonoid apigenin in Streptomyces albus J1074, with successful results in both cases, therefore expanding the current repertoire of genetic manipulation tools in Streptomyces species.

Indexed as

Anti-Bacterial AgentsApigeninBioreactorsDrug Resistance, BacterialEscherichia coliGenetic EngineeringGenetic VectorsNebramycinPlasmidsReplication OriginStreptomycesAnti-Bacterial AgentsApigeninapramycinNebramycinapigenin productionflavonoidsPseudomonas putidaSEVAshuttle vectorsstandardsStreptomycessynthetic biology

Identifiers

PMID32170856
PMCPMC7294301
OpenAlexW3012494287

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.