Evidence map›Paper›PMID 26201745›Full record

ArticleNature chemistry2015

Optimization of a whole-cell biocatalyst by employing genetically encoded product sensors inside nanolitre reactors.

Andreas Meyer, René Pellaux, Sébastien Potot, Katja Becker, Hans-Peter Hohmann, Sven Panke, Martin Held

Abstract read
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In one paragraph

Article in Nature chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Riboswitches, from cognition to transformation.Synthetic and systems biotechnology · 2023
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Droplet Microfluidics for Microbial Biotechnology.Advances in biochemical engineering/biotechnology · 2022
    Article
  15. Review
  16. Article
  17. Review
  18. Emerging Molecular Tools for Engineering Phytomicrobiome.Indian journal of microbiology · 2021
    Review
  19. Review
  20. 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.

Andreas Meyer1] Department of Biosystems Science and Engineering, ETH Zurich, Basel 4058, Switzerland [2] FGen GmbH, Basel 4057, Switzerland.
René Pellaux1] Department of Biosystems Science and Engineering, ETH Zurich, Basel 4058, Switzerland [2] FGen GmbH, Basel 4057, Switzerland.
Sébastien PototDSM Nutritional Products, Kaiseraugst 4303, Switzerland.
Katja BeckerDepartment of Biosystems Science and Engineering, ETH Zurich, Basel 4058, Switzerland.
Hans-Peter HohmannDSM Nutritional Products, Kaiseraugst 4303, Switzerland.
Sven PankeDepartment of Biosystems Science and Engineering, ETH Zurich, Basel 4058, Switzerland.
Martin HeldDepartment of Biosystems Science and Engineering, ETH Zurich, Basel 4058, Switzerland.ORCID 0000000259525659
ETH Zurich · CHDSM (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microcompartmentalization offers a high-throughput method for screening large numbers of biocatalysts generated from genetic libraries. Here we present a microcompartmentalization protocol for benchmarking the performance of whole-cell biocatalysts. Gel capsules served as nanolitre reactors (nLRs) for the cultivation and analysis of a library of Bacillus subtilis biocatalysts. The B. subtilis cells, which were co-confined with E. coli sensor cells inside the nLRs, converted the starting material cellobiose into the industrial product vitamin B2. Product formation triggered a sequence of reactions in the sensor cells: (1) conversion of B2 into flavin mononucleotide (FMN), (2) binding of FMN by a RNA riboswitch and (3) self-cleavage of RNA, which resulted in (4) the synthesis of a green fluorescent protein (GFP). The intensity of GFP fluorescence was then used to isolate B. subtilis variants that convert cellobiose into vitamin B2 with elevated efficiency. The underlying design principles of the assay are general and enable the development of similar protocols, which ultimately will speed up the optimization of whole-cell biocatalysts.

Indexed as

Bacillus subtilisBiosensing TechniquesEnzymesEscherichia coliFlavin MononucleotideNanostructuresEnzymesFlavin Mononucleotide

Identifiers

PMID26201745
OpenAlexW1021108028

What OpenQuestion holds

Textmetadata
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.