Evidence map›Paper›PMID 35355096›Full record

ArticleApplied microbiology and biotechnology2022

Biotransformation of artemisinin to a novel derivative via ring rearrangement by Aspergillus niger.

Jiaer Luo, Rebecca Mobley, Sian Woodfine, Falko Drijfhout, Paul Horrocks, Xiao-Dong Ren, Wen-Wu Li

Open access · hybridAbstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Biotransformation of Ursonic Acid byMolecules (Basel, Switzerland) · 2023
    Article
  6. Article
  7. 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

7 authors at 2 institutions in 2 countries.

Jiaer LuoDepartment of Biopharmacy, School of Life Science, Jilin University, Changchun, 130012, China.
Rebecca MobleySchool of Medicine, Keele University, Staffordshire, ST5 5BG, UK.
Sian WoodfineChemical Sciences Research Centre, Keele University, Staffordshire, ST5 5BG, UK.
Falko DrijfhoutChemical Sciences Research Centre, Keele University, Staffordshire, ST5 5BG, UK.
Paul HorrocksSchool of Medicine, Keele University, Staffordshire, ST5 5BG, UK.
Xiao-Dong RenDepartment of Biopharmacy, School of Life Science, Jilin University, Changchun, 130012, China. renxiaodong@jlu.edu.cn.
Wen-Wu LiSchool of Pharmacy and Bioengineering, Keele University, Stoke-on-Trent, ST4 7QB, UK. w.li@keele.ac.uk.ORCID http://orcid.org/0000-0002-3706-6068
Keele University · GBJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Artemisinin is a component part of current frontline medicines for the treatment of malaria. The aim of this study is to make analogues of artemisinin using microbial transformation and evaluate their in vitro antimalarial activity. A panel of microorganisms were screened for biotransformation of artemisinin (1). The biotransformation products were extracted, purified and isolated using silica gel column chromatography and semi-preparative HPLC. Spectroscopic methods including LC-HRMS, GC-MS, FT-IR, 1D and 2D NMR were used to elucidate the structure of the artemisinin metabolites.

Indexed as

AntimalarialsArtemisininsAspergillusAspergillus nigerBiotransformationMolecular StructureSpectroscopy, Fourier Transform InfraredAntimalarialsartemisininArtemisininsAnti-plasmodial activityArtemisininAspergillus nigerBiotransformationKinetics

Identifiers

PMID35355096
PMCPMC8989930
OpenAlexW4220790402

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.