Evidence map›Paper›PMID 26645909›Full record

ArticlePlant signaling & behavior2016

Benzoxazolinone detoxification by N-Glucosylation: The multi-compartment-network of Zea mays L.

Margot Schulz, Barbara Filary, Sabine Kühn, Thomas Colby, Anne Harzen, Jürgen Schmidt, Dieter Sicker, Lothar Hennig, Diana Hofmann, Ulrich Disko and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Plant signaling & behavior, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. The Apoplastic Secretome ofFrontiers in plant science · 2018
    Article
  4. 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

11 authors at 4 institutions in 1 country.

Margot Schulza IMBIO Institut für Biotechnologie der Pflanzen, Universität Bonn , Karlrobert Kreiten Str. 13, 53115 Bonn , Germany.
Barbara Filarya IMBIO Institut für Biotechnologie der Pflanzen, Universität Bonn , Karlrobert Kreiten Str. 13, 53115 Bonn , Germany.
Sabine Kühna IMBIO Institut für Biotechnologie der Pflanzen, Universität Bonn , Karlrobert Kreiten Str. 13, 53115 Bonn , Germany.
Thomas Colbyb Max-Planck-Institut für Pflanzenzüchtungsforschung, Carl von Linné Weg 10 , 50829 Köln , Germany.
Anne Harzend Institut für Organische Chemie, Universität Leipzig, Johannisallee 29 , 04103 Leipzig , Germany.
Jürgen Schmidta IMBIO Institut für Biotechnologie der Pflanzen, Universität Bonn , Karlrobert Kreiten Str. 13, 53115 Bonn , Germany.
Dieter Sickerd Institut für Organische Chemie, Universität Leipzig, Johannisallee 29 , 04103 Leipzig , Germany.
Lothar Hennigd Institut für Organische Chemie, Universität Leipzig, Johannisallee 29 , 04103 Leipzig , Germany.
Diana Hofmanne IBG-3: Agrossphäre, Forschungszentrum Jülich GmbH , 52428 Jülich , Germany.
Ulrich Diskoe IBG-3: Agrossphäre, Forschungszentrum Jülich GmbH , 52428 Jülich , Germany.
Nico Andersf AVT-Enzyme Process Technology, RWTH Aachen University, Worringer Weg 1 , 52074 Aachen , Germany.
Leipzig University · DEForschungszentrum Jülich · DEMax Planck Institute for Biology of Ageing · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The major detoxification product in maize roots after 24 h benzoxazolin-2(3H)-one (BOA) exposure was identified as glucoside carbamate resulting from rearrangement of BOA-N-glucoside, but the pathway of N-glucosylation, enzymes involved and the site of synthesis were previously unknown. Assaying whole cell proteins revealed the necessity of H2O2 and Fe(2+) ions for glucoside carbamate production. Peroxidase produced BOA radicals are apparently formed within the extraplastic space of the young maize root. Radicals seem to be the preferred substrate for N-glucosylation, either by direct reaction with glucose or, more likely, the N-glucoside is released by glucanase/glucosidase catalyzed hydrolysis from cell wall components harboring fixed BOA. The processes are accompanied by alterations of cell wall polymers. Glucoside carbamate accumulation could be suppressed by the oxireductase inhibitor 2-bromo-4´-nitroacetophenone and by peroxidase inhibitor 2,3-butanedione. Alternatively, activated BOA molecules with an open heterocycle may be produced by microorganisms (e.g., endophyte Fusarium verticillioides) and channeled for enzymatic N-glucosylation. Experiments with transgenic Arabidopsis lines indicate a role of maize glucosyltransferase BX9 in BOA-N-glycosylation. Western blots with BX9 antibody demonstrate the presence of BX9 in the extraplastic space. Proteomic analyses verified a high BOA responsiveness of multiple peroxidases in the apoplast/cell wall. BOA incubations led to shifting, altered abundances and identities of the apoplast and cell wall located peroxidases, glucanases, glucosidases and glutathione transferases (GSTs). GSTs could function as glucoside carbamate transporters. The highly complex, compartment spanning and redox-regulated glucoside carbamate pathway seems to be mainly realized in Poaceae. In maize, carbamate production is independent from benzoxazinone synthesis.

Indexed as

AcetophenonesArabidopsisBenzoxazolesBiological AssayBlotting, WesternCarbamatesCell WallChromatography, High Pressure LiquidCytosolDiacetylEthacrynic AcidFusariumGlucosidesGlutathione TransferaseGlycosylationInactivation, Metabolic2-bromo-4'-nitroacetophenoneAcetophenonesBenzoxazolesbenzoxazoloneCarbamatesDiacetylEthacrynic AcidGlucosidesGlutathione TransferasePeroxidasesPlant ProteinsBenzoxazolinone detoxificationcell wall polymerextraplastic spaceglucanaseglucoside carbamate pathwayperoxidaseprotein shiftingZea mays L

Identifiers

PMID26645909
PMCPMC4871689
OpenAlexW2260968953

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.