Evidence map›Paper›PMID 26334599›Full record

ArticlePhotosynthesis research2016

Metabolic engineering of Dunaliella salina for production of ketocarotenoids.

N Anila, Daris P Simon, Arun Chandrashekar, G A Ravishankar, R Sarada

Abstract read
PubMed Publisher
In one paragraph

Article in Photosynthesis research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

21 citing papers in PubMed, 75 citations in OpenAlex.

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  13. Article
  14. Strategies for enhancing terpenoids accumulation in microalgae.Applied microbiology and biotechnology · 2021
    Review
  15. Article
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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

5 authors at 4 institutions in 1 country.

N AnilaDepartment of Botany, St. Xavier's College For Women (Affiliated to Mahatma Gandhi University), Aluva, 683101, India.
Daris P SimonPlant Cell Biotechnology Department, Central Food Technological Research Institute (A Constituent Laboratory of the Council of Scientific and Industrial Research, CSIR), Mysore, Karnataka, 570 020, India.
Arun ChandrashekarBhat Bio-Tech India (P) Ltd., 11-A, 4th Cross Veerasandra Industrial Area Electronics City, Bangalore, 561221, India.
G A RavishankarDr. C. D. Sagar Center for Life Sciences, Dayanada Sagar Institutions, Bangalore, 560008, India.
R SaradaPlant Cell Biotechnology Department, Central Food Technological Research Institute (A Constituent Laboratory of the Council of Scientific and Industrial Research, CSIR), Mysore, Karnataka, 570 020, India. sarada_ravi@yahoo.com.
Central Food Technological Research Institute · INCouncil of Scientific and Industrial Research · INDr. Hari Singh Gour University · INSt Xavier’s College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dunaliella is a commercially important marine alga producing high amount of β-carotene. The use of Dunaliella as a potential transgenic system for the production of recombinant proteins has been recently recognized. The present study reports for the first time the metabolic engineering of carotenoid biosynthesis in Dunaliella salina for ketocarotenoid production. The pathway modification included the introduction of a bkt gene from H. pluvialis encoding β-carotene ketolase (4,4'β-oxygenase) along with chloroplast targeting for the production of ketocarotenoids. The bkt under the control of Dunaliella Rubisco smaller subunit promoter along with its transit peptide sequence was introduced into the alga through standardized Agrobacterium-mediated transformation procedure. The selected transformants were confirmed using GFP and GUS expression, PCR and southern blot analysis. A notable upregulation of the endogenous hydroxylase level of transformants was observed where the BKT expression was higher in nutrient-limiting conditions. Carotenoid analysis of the transformants through HPLC and MS analysis showed the presence of astaxanthin and canthaxanthin with maximum content of 3.5 and 1.9 µg/g DW, respectively. The present study reports the feasibility of using D. salina for the production of ketocarotenoids including astaxanthin.

Indexed as

Blotting, NorthernBlotting, SouthernCarotenoidsChlorophytaChromatography, High Pressure LiquidChromatography, Thin LayerGene Expression ProfilingGenes, PlantMass SpectrometryMetabolic EngineeringPolymerase Chain ReactionTransformation, GeneticCarotenoidsAstaxanthinCarotenoidsDunaliellaMetabolic engineering

Identifiers

PMID26334599
OpenAlexW1231798867

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.