Evidence map›Paper›PMID 25239975›Full record

ArticleEukaryotic cell2014

A high-throughput fatty acid profiling screen reveals novel variations in fatty acid biosynthesis in Chlamydomonas reinhardtii and related algae.

Erin L Pflaster, Michael J Schwabe, Joyanne Becker, Melissa S Wilkinson, Ashley Parmer, Thomas E Clemente, Edgar B Cahoon, Wayne R Riekhof

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Biochemical profiling of three indigenousBiotechnology reports (Amsterdam, Netherlands) · 2020
    Article
  5. Review
  6. 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

8 authors at 1 institution in 1 country.

Erin L PflasterSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Michael J SchwabeSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Joyanne BeckerSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA Department of Biological Sciences, Grinnell College, Grinnell, Iowa, USA.
Melissa S WilkinsonSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Ashley ParmerSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA Department of Biological Sciences, Fort Valley State University, Fort Valley, Georgia, USA.
Thomas E ClementeCenter for Plant Science Innovation, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Edgar B CahoonCenter for Plant Science Innovation, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Wayne R RiekhofSchool of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, USA wriekhof2@unl.edu.
University of Nebraska–Lincoln · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analysis of fatty acid methyl esters (FAMEs) by gas chromatography (GC) is a common technique for the quantitative and qualitative analysis of acyl lipids. Methods for FAME preparation are typically time-consuming and labor-intensive and require multiple transfers of reagents and products between reaction tubes and autosampler vials. In order to increase throughput and lower the time and materials costs required for FAME preparation prior to GC analysis, we have developed a method in which 10-to-20-mg samples of microbial biomass are transferred to standard GC autosampler vials, transesterified using an emulsion of methanolic trimethylsulfonium hydroxide and hexane, and analyzed directly by GC without further sample handling. This method gives results that are essentially identical to those obtained by the more labor- and material-intensive FAME preparation methods, such as transmethylation with methanolic HCl. We applied this method to the screening of laboratory and environmental isolates of the green alga Chlamydomonas for variations in fatty acid composition. This screening method facilitated two novel discoveries. First, we identified a common laboratory strain of C. reinhardtii, CC-620, completely lacking all ω-3 fatty acids normally found in this organism and showed that this strain contains an inactivating mutation in the CrFAD7 gene, encoding the sole ω-3 desaturase activity in this organism. Second, we showed that some species of Chlamydomonas make Δ6-unsaturated polyunsaturated fatty acids (PUFA) rather than the Δ5 species normally made by the previously characterized laboratory strains of Chlamydomonas, suggesting that there is species-specific variation in the regiospecificity and substrate selectivity of front-end desaturases in this algal genus.

Indexed as

Amino Acid SequenceChlamydomonas reinhardtiiChromatography, GasFatty Acid DesaturasesFatty Acids, UnsaturatedHexanesSequence AlignmentSubstrate SpecificitySulfonium CompoundsFatty Acid DesaturasesFatty Acids, UnsaturatedHexanesomega-3 fatty acid desaturaseSulfonium Compoundstrimethylsulfonium

Identifiers

PMID25239975
PMCPMC4248691
OpenAlexW2156455533

What OpenQuestion holds

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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.