Literature DB >> 35165789

Cinnabarinic acid from Trametes coccinea fruiting bodies exhibits antibacterial activity through inhibiting the biofilm formation.

Merilin Kakoti1,2, Samim Dullah2, Dibya Jyoti Hazarika2,3, Madhumita Barooah2, Robin Chandra Boro4.   

Abstract

Wild mushrooms are rich sources of natural compounds with potent bioactive properties. Several important metabolites have been reported from mushrooms, which possess clinically important bioactive properties like antibacterial, anticancer, antidiabetic, and neuroprotective activity. In this study, we have evaluated the antimicrobial activity of Trametes coccinea fruiting body extracts against different bacterial isolates, viz., Bacillus subtilis, Bacillus cereus, and Escherichia coli. Fruiting bodies of three T. coccinea samples, of which two were collected from Santipur, Arunachal Pradesh and one collected from Jorhat, Assam, were used for extraction using methanol. The extracts showed significant antimicrobial activity against all the test bacteria. Minimum Inhibitory Concentration (MIC) of the extracts against Bacillus subtilis, Bacillus cereus, and Escherichia coli was recorded as 400 µg/ml, 400 µg/ml, and 300 µg/ml, respectively. Furthermore, the bioactive compounds of the extract were separated and detected using Thin Layer Chromatography (TLC). Presence of cinnabarinic acid (CBA)-a potent antimicrobial compound- was detected in TLC, which was further confirmed through High Performance Liquid Chromatography (HPLC) and Electrospray Ionization-Mass Spectrometry (ESI-MS). Cinnabarinic acid was able to inhibit the formation of biofilms in Bacillus subtilis and B. cereus, suggesting that the compound can be beneficial in the management of biofilm-based antimicrobial resistance.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Antimicrobial; Bioactive metabolites; Biofilm formation; Cinnabarinic acid; Trametes coccinea

Mesh:

Substances:

Year:  2022        PMID: 35165789     DOI: 10.1007/s00203-022-02782-4

Source DB:  PubMed          Journal:  Arch Microbiol        ISSN: 0302-8933            Impact factor:   2.552


  22 in total

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Authors:  Salman Y Jabri; Larry E Overman
Journal:  J Org Chem       Date:  2013-08-27       Impact factor: 4.354

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Authors:  C Eggert
Journal:  Microbiol Res       Date:  1997-09       Impact factor: 5.415

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Journal:  FEBS Lett       Date:  1996-08-05       Impact factor: 4.124

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Authors:  Rie Hiramatsu; Toshiaki Hara; Hidetoshi Akimoto; Osamu Takikawa; Tsutomu Kawabe; Ken-Ichi Isobe; Fumihiko Nagase
Journal:  J Cell Biochem       Date:  2008-01-01       Impact factor: 4.429

7.  Effect of farnesol on planktonic and biofilm cells of Staphylococcus epidermidis.

Authors:  Fernanda I A Gomes; Pilar Teixeira; Joana Azeredo; Rosário Oliveira
Journal:  Curr Microbiol       Date:  2009-04-14       Impact factor: 2.188

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Authors:  C Eggert; U Temp; J F Dean; K E Eriksson
Journal:  FEBS Lett       Date:  1995-12-04       Impact factor: 4.124

9.  Serratia Secondary Metabolite Prodigiosin Inhibits Pseudomonas aeruginosa Biofilm Development by Producing Reactive Oxygen Species that Damage Biological Molecules.

Authors:  Önder Kimyon; Theerthankar Das; Amaye I Ibugo; Samuel K Kutty; Kitty K Ho; Jan Tebben; Naresh Kumar; Mike Manefield
Journal:  Front Microbiol       Date:  2016-06-27       Impact factor: 5.640

10.  Prodigiosin inhibits motility and activates bacterial cell death revealing molecular biomarkers of programmed cell death.

Authors:  N Darshan; H K Manonmani
Journal:  AMB Express       Date:  2016-07-26       Impact factor: 3.298

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