Evidence map›Paper›PMID 36178376›Full record

ArticlePest management science2023

Inhibition profile of trifludimoxazin towards PPO2 target site mutations.

Aimone Porri, Michael Betz, Kathryn Seebruck, Michael Knapp, Philipp Johnen, Matthias Witschel, Raphael Aponte, Rex Liebl, Patrick J Tranel, Jens Lerchl

Open access · hybridAbstract read
In one paragraph

Article in Pest management science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

3 citing papers in PubMed, 24 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Aimone PorriBASF SE, Ludwigshafen am Rhein, Germany.ORCID https://orcid.org/0000-0001-7846-6722
Michael BetzBASF SE, Ludwigshafen am Rhein, Germany.
Kathryn SeebruckDepartment of Crop Sciences, University of Illinois at Urbana-Champaign College of Agricultural, Consumer and Environmental Sciences, Urbana, Illinois, USA.
Michael KnappBASF SE, Ludwigshafen am Rhein, Germany.
Philipp JohnenBASF SE, Ludwigshafen am Rhein, Germany.ORCID https://orcid.org/0000-0002-4512-9508
Matthias WitschelBASF SE, Ludwigshafen am Rhein, Germany.
Raphael AponteBASF Corporation, Research Triangle Park, North Carolina, USA.
Rex LieblBASF Corporation, Research Triangle Park, North Carolina, USA.
Patrick J TranelDepartment of Crop Sciences, University of Illinois at Urbana-Champaign College of Agricultural, Consumer and Environmental Sciences, Urbana, Illinois, USA.ORCID https://orcid.org/0000-0003-0666-4564
Jens LerchlBASF SE, Ludwigshafen am Rhein, Germany.
BASF (Germany) · DEResearch Triangle Park Foundation · USUniversity of Illinois Urbana-Champaign · US

Funding

The USDA National Institute of Food and Agriculture provided partial funding of this research HatchProjectILLU-802-944
6 · The paper itself

Abstract

backgroundTarget site resistance to herbicides that inhibit protoporphyrinogen IX oxidase (PPO; EC 1.3.3.4) has been described mainly in broadleaf weeds based on mutations in the gene designated protoporphyrinogen oxidase 2 (PPO2) and in one monocot weed species in protoporphyrinogen oxidase 1 (PPO1). To control PPO target site resistant weeds in future it is important to design new PPO-inhibiting herbicides that can control problematic weeds expressing mutant PPO enzymes. In this study, we assessed the efficacy of a new triazinone-type inhibitor, trifludimoxazin, to inhibit PPO2 enzymes carrying target site mutations in comparison with three widely used PPO-inhibiting herbicides.

resultsMutated Amaranthus spp. PPO2 enzymes were expressed in Escherichia coli, purified and measured biochemically for activity and inhibition kinetics, and used for complementation experiments in an E. coli hemG mutant that lacks the corresponding microbial PPO gene function. In addition, we used ectopic expression in Arabidopsis and structural PPO protein modeling to support the enzyme inhibition study. The generated data strongly suggest that trifludimoxazin is a strong inhibitor both at the enzyme level and in transgenics Arabidopsis ectopically expressing PPO2 target site mutations.

conclusionTrifludimoxazin is a potent PPO-inhibiting herbicide that inhibits various PPO2 enzymes carrying target site mutations and could be used as a chemical-based control strategy to mitigate the widespread occurrence of PPO target site resistance as well as weeds that have evolved resistance to other herbicide mode of actions. © 2022 BASF SE and The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Indexed as

ArabidopsisHerbicidesEscherichia coliHerbicide ResistanceMutationPlant WeedsProtoporphyrinogen OxidaseHerbicidesProtoporphyrinogen Oxidaseefficacyherbicideherbicide resistancemutationsPPOtarget sitetrifludimoxazin

Identifiers

PMID36178376
PMCPMC10092844
OpenAlexW4298087960

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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.