Evidence map›Paper›PMID 26168783›Full record

ArticleNature communications2015

A highly selective biosynthetic pathway to non-natural C50 carotenoids assembled from moderately selective enzymes.

Maiko Furubayashi, Mayu Ikezumi, Shinichi Takaichi, Takashi Maoka, Hisashi Hemmi, Takuya Ogawa, Kyoichi Saito, Alexander V Tobias, Daisuke Umeno

Abstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Biochemical and Immunological implications of Lutein and Zeaxanthin.International journal of molecular sciences · 2021
    Review
  12. Production of Rainbow Colorants by Metabolically Engineered Escherichia coli.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  13. Article
  14. Review
  15. Modular engineering for microbial production of carotenoids.Metabolic engineering communications · 2020
    Review
  16. Article
  17. Review
  18. Article
  19. Discovery and engineering of an endophyticJournal of biological engineering · 2019
    Article
  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

9 authors.

Maiko FurubayashiDepartment of Applied Chemistry and Biotechnology, Chiba University, Chiba 263-8522, Japan.
Mayu IkezumiDepartment of Applied Chemistry and Biotechnology, Chiba University, Chiba 263-8522, Japan.
Shinichi TakaichiDepartment of Biology, Nippon Medical School, Musashino, Tokyo 180-0023, Japan.
Takashi MaokaResearch Institute for Production Development, Kyoto 606-0805, Japan.
Hisashi HemmiDepartment of Applied Molecular Biosciences, Nagoya University, Nagoya 464-8601, Japan.
Takuya OgawaDepartment of Applied Molecular Biosciences, Nagoya University, Nagoya 464-8601, Japan.
Kyoichi SaitoDepartment of Applied Chemistry and Biotechnology, Chiba University, Chiba 263-8522, Japan.
Alexander V TobiasDuPont Industrial Biosciences, Experimental Station, Wilmington, Delaware 19803, USA.
Daisuke Umeno1] Department of Applied Chemistry and Biotechnology, Chiba University, Chiba 263-8522, Japan [2] Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Saitama 332-0012, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synthetic biology aspires to construct natural and non-natural pathways to useful compounds. However, pathways that rely on multiple promiscuous enzymes may branch, which might preclude selective production of the target compound. Here, we describe the assembly of a six-enzyme pathway in Escherichia coli for the synthesis of C50-astaxanthin, a non-natural purple carotenoid. We show that by judicious matching of engineered size-selectivity variants of the first two enzymes in the pathway, farnesyl diphosphate synthase (FDS) and carotenoid synthase (CrtM), branching and the production of non-target compounds can be suppressed, enriching the proportion of C50 backbones produced. We then further extend the C50 pathway using evolved or wild-type downstream enzymes. Despite not containing any substrate- or product-specific enzymes, the resulting pathway detectably produces only C50 carotenoids, including ∼ 90% C50-astaxanthin. Using this approach, highly selective pathways can be engineered without developing absolutely specific enzymes.

Indexed as

Bacterial ProteinsBiosynthetic PathwaysCarotenoidsEscherichia coliEscherichia coli ProteinsFarnesyl-Diphosphate FarnesyltransferaseGeranyltranstransferaseXanthophyllsastaxanthineBacterial ProteinsCarotenoidsCrtM protein, Staphylococcus aureusEscherichia coli ProteinsFarnesyl-Diphosphate FarnesyltransferaseGeranyltranstransferaseXanthophylls

Identifiers

PMID26168783
PMCPMC4510654

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.