Evidence map›Paper›PMID 41028578›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

A Method for Isolation and Transfection of Arabidopsis Protoplast for Sucrose Feeding Assay.

Anjali Anjali, Muthappa Senthil-Kumar

Abstract read
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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Anjali AnjaliBRIC-National Institute of Plant Genome Research, New Delhi, Delhi, India.
Muthappa Senthil-KumarBRIC-National Institute of Plant Genome Research, New Delhi, Delhi, India. skmuthappa@nipgr.ac.in.ORCID https://orcid.org/0000-0003-1502-1659

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protoplasts serve as a powerful system to study various plant physiological processes and to understand crucial signaling pathways within the plant system. The isolation of Arabidopsis protoplasts is a well-established technique and being utilized for wide range of assays. The method described herein includes the precise cutting of Arabidopsis leaves using extraction buffer containing cellulase and macerozyme. Further we present a polyethylene glycol [PEG]-mediated protoplast transformation method. Here, we have elucidated the methodology for isolation of protoplast for the AtSWEET-mediated sucrose uptake assay in control, and Pseudomonas syringe pv tomato DC3000 (Pst DC3000) treated leaves by utilizing GC/MS analysis. Our approach includes certain modifications to the previously published protoplast isolation technique, streamlining the process and providing a more accessible alternative to the highly specialized Xenopus oocyte uptake assay.

Indexed as

ArabidopsisProtoplastsSucroseTransfectionAnimalsPlant LeavesPolyethylene GlycolsPolyethylene GlycolsSucroseArabidopsis thalianaMembrane proteinPlant-pathogen interactionProtoplastPseudomonas syringae pv tomatoSugar transport

Identifiers

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.