Evidence map›Paper›PMID 37743438›Full record

ArticleWorld journal of microbiology & biotechnology2023

Molecular docking and antibacterial activity of Sargassum fusiforme extracts against major coral pathogens.

Nedaa Ahmed, Mohamed A M El-Tabakh, Hala F Mohamed, Xudong Wu, Changan Xu, Lingfeng Huang

Abstract read
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In one paragraph

Article in World journal of microbiology & biotechnology, 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
1.7field-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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Marine algae-derived Ag/AlJournal of materials science. Materials in medicine · 2026
    Article
  3. 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

6 authors at 2 institutions in 2 countries.

Nedaa AhmedThird Institute of Oceanography, Ministry of Natural Resources, Xiamen, 361005, People's Republic of China. nedaahussain.5922@azhar.edu.eg.
Mohamed A M El-TabakhFaculty of Science, Marine Biology and Ichthyology Branch, Zoology Department (Boys Branch), Al-Azhar University, Cairo, Egypt.
Hala F MohamedThird Institute of Oceanography, Ministry of Natural Resources, Xiamen, 361005, People's Republic of China.
Xudong WuThird Institute of Oceanography, Ministry of Natural Resources, Xiamen, 361005, People's Republic of China.
Changan XuThird Institute of Oceanography, Ministry of Natural Resources, Xiamen, 361005, People's Republic of China.
Lingfeng HuangCollege of the Environment & Ecology, Xiamen University, Xiang'an district, Xiamen, 361102, People's Republic of China.
Fujian Institute of Oceanography · CNAl-Azhar University · EG

Funding

China Asia-Pacific Economic Cooperation HV180101 and HV01-190101Specific Fund Project of Xiamen Marine and Fishery Development 19CZP011HJ08Xiamen Science and Technology Program 3502Z20161162
6 · The paper itself

Abstract

The present study evaluates the antibacterial properties of alkaloids and the crude extracts (ethanol, n-hexane and ethyl acetate) from seaweed Sargassum fusiforme against coral pathogens (Photobacterium galatheae, Vibrio harveyi, Bordetella trematum, and Ochrobactrum pseudogrignonese) isolated from coral Porites lutea. To our knowledge, this is the first in vitro assay for such extracts on Porites lutea coral pathogens. Bacterial pathogens have been identified using 16S RNA and BankIt into gene bank and given the accession numbers (OR401000; OR401001; OR401336, and OR400998 respectively). GC-Mass profiling conducted for n-hexane compounds confirmed the presence of thirty-eight molecules, twelve of which have been previously reported for their bioactivity. The results revealed that alkaloids and n-hexane extract demonstrated eminent antibacterial activity compared to the other extracts against the tested coral pathogenic bacteria. Molecular docking was conducted to evaluate the twelve previously mentioned bioactive molecules to get a full understanding of the interaction of those bioactive molecules on vital bacterial proteins (Hemolysin protein (PDB ID: 1XEZ) and Cytoplasmic proteins (PDB ID: 3TZC)). Docked twelve molecules against hemolysin protein (PDB ID: 1XEZ) came exactly in line with the docked result of the same molecules with cytoplasmic proteins (PDB ID: 3TZC), proving the bioactivity of 6-O-Palmitoyl-L-ascorbic acid, 3TMS derivative; Glycerol monostearate, 2TMS derivative and Eicosanoic acid complexes in antibacterial activity action and score higher than reference ligand. Those three compounds will be investigated separately in future in vitro assay soon. Our conclusions align with the study's antibacterial in vitro assay results. The present study reports the novelty of different extracts of S. fusiforme as an antibacterial agent against coral pathogenic bacteria that trigger diseases in Porites lutea.

Indexed as

AnthozoaHemolysin ProteinsAnimalsAnti-Bacterial AgentsEdible SeaweedsHexanesMolecular Docking SimulationSargassumAnti-Bacterial AgentsHemolysin ProteinsHexanesn-hexaneAntibacterial activityCoral pathogensDocking analysisn-hexanePorites luteaSargassum fusiforme

Identifiers

PMID37743438
OpenAlexW4386994095

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.