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International Journal of Medicinal Mushrooms
Импакт фактор: 1.423 5-летний Импакт фактор: 1.525 SJR: 0.431 SNIP: 0.716 CiteScore™: 2.6

ISSN Печать: 1521-9437
ISSN Онлайн: 1940-4344

Выпуски:
Том 22, 2020 Том 21, 2019 Том 20, 2018 Том 19, 2017 Том 18, 2016 Том 17, 2015 Том 16, 2014 Том 15, 2013 Том 14, 2012 Том 13, 2011 Том 12, 2010 Том 11, 2009 Том 10, 2008 Том 9, 2007 Том 8, 2006 Том 7, 2005 Том 6, 2004 Том 5, 2003 Том 4, 2002 Том 3, 2001 Том 2, 2000 Том 1, 1999

International Journal of Medicinal Mushrooms

DOI: 10.1615/IntJMedMushrooms.v17.i10.100
pages 1005-1017

Novel Bioactive Wild Medicinal Mushroom−Xylaria sp. R006 (Ascomycetes) against Multidrug Resistant Human Bacterial Pathogens and Human Cancer Cell Lines

Veluchamy Ramesh
Department of Botany, Vivekananda College, Tiruvedagam west, Madurai, Tamilnadu, India
Karnewar Santosh
Centre for Chemical Biology, CSIR-Indian Institute of Chemical Technology (IICT), Hyderabad, India
Thangarajan Durai Anand
Department of Microbial Technology, School of Biological Sciences, Madurai Kamaraj University, Madurai, Tamilnadu, India
Vellasamy Shanmugaiah
Department of Microbial Technology, School of Biological Sciences, Madurai Kamaraj University, Madurai, Tamilnadu, India
Srigiridhar Kotamraju
Centre for Chemical Biology, CSIR-Indian Institute of Chemical Technology (IICT), Hyderabad, India
Chandran Karunakaran
Department of Chemistry, Biomedical Research Lab, VHNSN College, Virudhunagar, Tamilnadu, India
Ayyappan Rajendran
Department of Botany, VHNSN College, Virudhunagar, Tamilnadu, India

Краткое описание

In the present study, the fruiting body extracts of Xylaria sp. strain R006 were obtained from hexane, ethyl acetate and methanol. Among them, the ethyl acetate extract exhibited significant antimicrobial activities against bacterial and fungal pathogens. Based on the effective antimicrobial activity, the crude ethyl acetate extract was fractionized by two-step siliga gel column chromatography. All the fractions were tested for antibacterial activity against drug resistant Staphylococcus aureus strains (1−10) and Pseudomonas aeruginosa strains (1−8). The fraction E showed a maximum inhibition zone of 27.9 mm against drug resistant S. aureus strain 3 and 29.4 mm against drug resistant P. aeruginosa strain 4. Minimal inhibitory concentration of fraction E showed potential result against all the drug resistant strains however, the lowest concentration of 75 µg/mL−1 was observed against S. aureus strains 1 and 6 and P. aeruginosa strain 3. Further, 60 µg/mL of fraction E had significant cytotoxic activity of 54.9, 55.1 and 54.9% against MDA-MB-231 (breast carcinoma cells), A-549 (lung carcinoma cells) and MCF-7 (breast carcinoma cells) human cancer cell lines, respectively. The spectral data revealed that the fraction E has chromophoric groups in it and had the C = O stretching, C−C = C asymmetric stretch, N-H stretch and C-O stretch as functional groups. The results indicate that the metabolites of fruiting bodies of Xylaria sp. R006 are the potential natural source for the development of new anticancer agents.


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