Evidence map›Paper›PMID 35695951›Full record

ArticleApplied biochemistry and biotechnology2022

4a-methyl-dodecahydro-1H-pyrrolo[3,4-b]quinoline-6-one produced by Endophytic Fungi Aspergillus niger E12 obtained from Dodonaea viscosa Plant Leaves as a Novel Antibacterial Compound.

Manickam Ramesh, Kuppuswamy Kavitha, Arumugam Rajalakshmi, Elamaran Anjukam, Vadivel Prabakaran, Mani Prakash, Rengarajulu Puvanakrishnan, Balasubramanian Ramesh

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Article in Applied biochemistry and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 1 country.

Manickam RameshResearch Department of Biotechnology, Sri Sankara Arts and Science College, Kanchipuram, 631561, Tamil Nadu, India.
Kuppuswamy KavithaResearch Department of Microbiology, Sri Sankara Arts and Science College, Kanchipuram, 631561, Tamil Nadu, India.
Arumugam RajalakshmiResearch Department of Biotechnology, Sri Sankara Arts and Science College, Kanchipuram, 631561, Tamil Nadu, India.
Elamaran AnjukamResearch Department of Biotechnology, Sri Sankara Arts and Science College, Kanchipuram, 631561, Tamil Nadu, India.
Vadivel PrabakaranResearch Department of Biotechnology, Sri Sankara Arts and Science College, Kanchipuram, 631561, Tamil Nadu, India.
Mani PrakashResearch Department of Microbiology, Kanchi Shri Krishna College of Arts and Science, Kanchipuram, 631551, Tamil Nadu, India.
Rengarajulu PuvanakrishnanResearch Department of Biotechnology, Sri Sankara Arts and Science College, Kanchipuram, 631561, Tamil Nadu, India.
Balasubramanian RameshResearch Department of Biotechnology, Sri Sankara Arts and Science College, Kanchipuram, 631561, Tamil Nadu, India. ramesh@sankaracollege.edu.in.ORCID http://orcid.org/0000-0003-0890-3178
Sankara Nethralaya · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endophytic fungi were isolated from forty plant leaf samples from Gudiyam forest. The potent antibacterial strain Aspergillus niger E12 isolated from the plant Dodonaea viscosa showed maximal antibacterial activity against all the test organisms, viz., Staphylococcus aureus, Bacillus coagulans, Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa. The production of the antibacterial compound was optimized using the yeast extract sucrose medium (2% YES) using response surface methodology (RSM). For the production, the optimal parameters were carbon/nitrogen (C:N) ratio, 9:1; temperature, 25 °C; pH, 5.7; incubation time, 240 h; and rpm, 30. A zone of inhibition of 19.33 mm was observed as maximal bioactivity against Pseudomonas aeruginosa. The antibacterial compound was purified by extraction with ethyl acetate, activity-guided fractionation, and preparative high-performance liquid chromatography (HPLC), gas chromatography-mass spectrometry (GC-MS), Fourier transform infrared (FTIR) spectroscopy, and nuclear magnetic resonance (NMR) studies showed that the Aspergillus niger E12 bioactive substance is 4a-methyl-dodecahydro-1H-pyrrolo [3,4-b] quinoline-6-one.

Indexed as

Anti-Bacterial AgentsQuinolinesAspergillus nigerCarbonEscherichia coliFungiMicrobial Sensitivity TestsNitrogenPlant LeavesPseudomonas aeruginosaSucroseAnti-Bacterial AgentsCarbonNitrogenQuinolinesSucroseAntibacterial activityChromatographyEndophytic fungiFTIRGC–MSNMRNovel quinolinone antibacterial compound

Identifiers

PMID35695951
OpenAlexW4282553791

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.