Multifarious Elicitors: Invoking Biosynthesis of Various Bioactive Secondary Metabolite in Fungi

Author(s):  
Preeti Bharatiya ◽  
Pooja Rathod ◽  
Aishwarya Hiray ◽  
Abhijeet S. Kate
Author(s):  
Mariana Costa Ferreira ◽  
Camila Rodrigues de Carvalho ◽  
Marina Bahia ◽  
Débora Luiza Costa Barreto ◽  
Rafaela Nogueira Azevedo ◽  
...  

2020 ◽  
Vol 16 (7) ◽  
pp. 1103-1107
Author(s):  
Fabiana Tonial ◽  
Charise D. Bertol ◽  
Beatriz H.L.N. Sales Maia ◽  
Josiane A.G. Figueiredo ◽  
Kielli C.F. Guerra ◽  
...  

Background: Motivated by the need for bioprospecting new drug studies have revealed a variety of secondary metabolites with biological activity. In particular, antimicrobial research confronts the growing reality of resistance of microorganisms to currently available drugs. Modifications in the chemical structure of secondary metabolites may be important in the development of a product to improve the efficacy of these compounds. Being cognizant of the fact that modifications in the chemical structure could enhance the biological activity and improve the compound characteristics for the development of a product, the present study aimed to verify, if there is the possibility of a significant difference in the bioactivity of verbanol in relation to verbenol. Methods: The biological activity was evaluated by agar diffusion assay and microdilution. Results: Verbanol is a bioactive secondary metabolite produced by the endophytic fungus Diaporthe terebinthifolli LGMF658. This compound has bactericidal activity against Staphylococcus aureus and fungicide against Candida albicans according to the microdilution assay. Discussion: In contrast, verbenol, a byproduct of verbanol, did not control the development of the bacterium and showed fungistatic activity against yeast. Conclusion: The results demonstrated that the presence of the double bond, which increased the polarity of the compound, reduced its bioactivity, corroborating with other studies that report the importance of lipophilicity for antimicrobial action.


1995 ◽  
Vol 38 (3) ◽  
pp. 595-597 ◽  
Author(s):  
Alberto Arnone ◽  
Gemma Assante ◽  
Michela Montorsi ◽  
Gianluca Nasini

2021 ◽  
Vol 16 (4) ◽  
pp. 1934578X2199172
Author(s):  
Pawan K. Agrawal ◽  
Chandan Agrawal ◽  
Gerald Blunden

Various computational studies, including in silico ones, have identified several existing compounds that could serve as effective inhibitors of the SARS-CoV-2 main protease (Mpro), and thus preventing replication of the virus. Among these, rutin has been identified as a potential hit, having prominent binding affinity to the virus. Moreover, its presence in several traditional antiviral medicines prescribed in China to infected patients with mild to moderate symptoms of COVID-19 justify its promise as a repurposed bioactive secondary metabolite against SARS-CoV-2.


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