Evidence map›Paper›PMID 35909773›Full record

ArticleFrontiers in plant science2022

Effective Mechanisms for Improving Seed Oil Production in Pennycress (

Christopher Johnston, Leidy Tatiana García Navarrete, Emmanuel Ortiz, Trevor B Romsdahl, Athanas Guzha, Kent D Chapman, Erich Grotewold, Ana Paula Alonso

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  9. Imaging plant metabolism in situ.Journal of experimental botany · 2024
    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

8 authors at 2 institutions in 1 country.

Christopher JohnstonDepartment of Biological Sciences, BioDiscovery Institute, University of North Texas, Denton, TX, United States.
Leidy Tatiana García NavarreteDepartment of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI, United States.
Emmanuel OrtizDepartment of Biological Sciences, BioDiscovery Institute, University of North Texas, Denton, TX, United States.
Trevor B RomsdahlDepartment of Biological Sciences, BioDiscovery Institute, University of North Texas, Denton, TX, United States.
Athanas GuzhaDepartment of Biological Sciences, BioDiscovery Institute, University of North Texas, Denton, TX, United States.
Kent D ChapmanDepartment of Biological Sciences, BioDiscovery Institute, University of North Texas, Denton, TX, United States.
Erich GrotewoldDepartment of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI, United States.
Ana Paula AlonsoDepartment of Biological Sciences, BioDiscovery Institute, University of North Texas, Denton, TX, United States.
University of North Texas · USMichigan State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pennycress is a potentially lucrative biofuel crop due to its high content of long-chain unsaturated fatty acids, and because it uses non-conventional pathways to achieve efficient oil production. However, metabolic engineering is required to improve pennycress oilseed content and make it an economically viable source of aviation fuel. Research is warranted to determine if further upregulation of these non-conventional pathways could improve oil production within the species even more, which would indicate these processes serve as promising metabolic engineering targets and could provide the improvement necessary for economic feasibility of this crop. To test this hypothesis, we performed a comparative biomass, metabolomic, and transcriptomic analyses between a high oil accession (HO) and low oil accession (LO) of pennycress to assess potential factors required to optimize oil content. An evident reduction in glycolysis intermediates, improved oxidative pentose phosphate pathway activity, malate accumulation in the tricarboxylic acid cycle, and an anaplerotic pathway upregulation were noted in the HO genotype. Additionally, higher levels of threonine aldolase transcripts imply a pyruvate bypass mechanism for acetyl-CoA production. Nucleotide sugar and ascorbate accumulation also were evident in HO, suggesting differential fate of associated carbon between the two genotypes. An altered transcriptome related to lipid droplet (LD) biosynthesis and stability suggests a contribution to a more tightly-packed LD arrangement in HO cotyledons. In addition to the importance of central carbon metabolism augmentation, alternative routes of carbon entry into fatty acid synthesis and modification, as well as transcriptionally modified changes in LD regulation, are key aspects of metabolism and storage associated with economically favorable phenotypes of the species.

Indexed as

ascorbatebiofuelcell wallcentral carbon metabolismerucic acid (C22:1)lipid dropletThlaspi arvensethreonine aldolase

Identifiers

PMID35909773
PMCPMC9330397
OpenAlexW4285495035

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.