Evidence map›Paper›PMID 24255853›Full record

ArticleSpringerPlus2013

Analyses of Arabidopsis ecotypes reveal metabolic diversity to convert D-amino acids.

Dirk Gördes, Grit Koch, Kerstin Thurow, Uner Kolukisaoglu

Abstract read
In one paragraph

Article in SpringerPlus, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. International journal of molecular sciences · 2020
    Review
  4. Article
  5. Article
  6. d-Amino Acids Are Exuded by Arabidopsis thaliana Roots to the Rhizosphere.International journal of molecular sciences · 2018
    Article
  7. Article
  8. Discovery of a novel amino acid racemase through exploration of natural variation in Arabidopsis thaliana.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

4 authors.

Dirk GördesInstitute of Automation, University of Rostock, Richard-Wagner-Str. 31, D-18119 Rostock, Germany ; WESSLING GmbH, Haynauer Straβe 60, 12249 Berlin, Germany.
Grit Koch
Kerstin Thurow
Uner Kolukisaoglu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For a long time D-enantiomers of proteinogenic L-amino acids were assumed to be physiologically irrelevant for plants. But there is growing evidence that D-amino acids (D-AAs) also fulfil important physiological functions in these organisms. However, the knowledge about the metabolic fate of D-AAs in plants is still scarce and more information about it is needed. To close this gap we established an optimized protocol for the processing and analysis of D- and L-AAs from large numbers of Arabidopsis lines. This included the application of 18 different D-AAs to seedlings, the extraction of free amino acids from the samples and the determination of 16 L-AAs and their corresponding D-enantiomers. To validate our approach we searched for genetic accessions with aberrant amino acid metabolism. Therefore we applied D-AAs on 17 ecotypes of Arabidopsis thaliana and analysed their free amino acid contents. These analyses confirmed the suitability of the system for the analysis of large sets of plant samples with enhanced velocity and improved accuracy. Furthermore, the resulting data led to the definition of standard amino acid profiles in response to D-AAs of Arabidopsis seedlings. Within these analyses the ecotype Landsberg erecta was found with aberrant metabolic patterns like drastically reduced capabilities to convert different D-AAs to D-alanine and D-glutamate. The presented experimental setup and results of this study offer starting points to dissect the metabolic pathway of D-AAs in plants.

Indexed as

Arabidopsis thalianaChiral separationD-amino acids in soil and plantsHigh performance liquid chromatographyL- and D-amino acidsMass spectrometry

Identifiers

PMID24255853
PMCPMC3825070

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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.