Evidence map›Paper›PMID 39609835›Full record

ArticleMicrobial cell factories2024

Genetic engineering of Nannochloropsis oceanica to produce canthaxanthin and ketocarotenoids.

Davide Canini, Flavio Martini, Stefano Cazzaniga, Tea Miotti, Beatrice Pacenza, Sarah D'Adamo, Matteo Ballottari

Abstract read
In one paragraph

Article in Microbial cell factories, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Microorganisms · 2025
    Article
  5. Article
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  8. Review
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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

7 authors.

Davide Canini *Dipartimento di Biotecnologie, Università Degli Studi di Verona, Strada le Grazie 15, 37134, Verona, Italy.
Flavio Martini *Dipartimento di Biotecnologie, Università Degli Studi di Verona, Strada le Grazie 15, 37134, Verona, Italy.
Stefano CazzanigaDipartimento di Biotecnologie, Università Degli Studi di Verona, Strada le Grazie 15, 37134, Verona, Italy.
Tea MiottiDipartimento di Biotecnologie, Università Degli Studi di Verona, Strada le Grazie 15, 37134, Verona, Italy.
Beatrice PacenzaDipartimento di Biotecnologie, Università Degli Studi di Verona, Strada le Grazie 15, 37134, Verona, Italy.
Sarah D'AdamoBioprocess Engineering Chair Group, Wageningen University and Research, Wageningen, 6700 AA, The Netherlands.
Matteo BallottariDipartimento di Biotecnologie, Università Degli Studi di Verona, Strada le Grazie 15, 37134, Verona, Italy. matteo.ballottari@univr.it.

Funding

HORIZON EUROPE European Innovation Council 101099476
6 · The paper itself

Abstract

backgroundCanthaxanthin is a ketocarotenoid with high antioxidant activity, and it is primarily produced by microalgae, among which Nannochloropsis oceanica, a marine alga widely used for aquaculture. In the last decade, N. oceanica has become a model organism for oleaginous microalgae to develop sustainable processes to produce biomolecules of interest by exploiting its photosynthetic activity and carbon assimilation properties. N. oceanica can accumulate lipids up to 70% of total dry weight and contains the omega-3 fatty acid eicosapentaenoic acid (EPA) required for both food and feed applications. The genome sequence, other omics data, and synthetic biology tools are available for this species, including an engineered strain called LP-tdTomato, which allows homologous recombination to insert the heterologous genes in a highly transcribed locus in the nucleolus region. Here, N. oceanica was engineered to induce high ketocarotenoid and canthaxanthin production.

resultsWe used N. oceanica LP-tdTomato strain as a background to express the key enzyme for ketocarotenoid production, a β-carotene ketolase (CrBKT) from Chlamydomonas reinhardtii. Through the LP-tdTomato strain, the transgene insertion by homologous recombination in a highly transcribed genomic locus can be screened by negative fluorescence. The overexpression of CrBKT in bkt transformants increased the content of carotenoids and ketocarotenoids per cell, respectively, 1.5 and 10-fold, inducing an orange/red color in the bkt cell cultures. Background (LP) and bkt lines productivity were compared at different light intensities from 150 to 1200 µmol m

conclusionsThrough targeted gene redesign and heterologous transformation, ketocarotenoids and canthaxanthin content were significantly increased, achieving 0.3% and 0.2% dry weight. Canthaxanthin could be produced using CO

Indexed as

CanthaxanthinCarotenoidsChlamydomonas reinhardtiiGenetic EngineeringMetabolic EngineeringMicroalgaeOxygenasesStramenopilesbeta-carotene ketolaseCanthaxanthinCarotenoidsOxygenasesCanthaxanthinCarotenoidsKetocarotenoidsMicroalgaeNannochloropsis

Identifiers

PMID39609835
PMCPMC11606307

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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.