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Analysis of the Bioactive Metabolites of the Endangered Mexican Lost Fungi Campanophyllum - A Report from India 원문보기

Mycobiology, v.48 no.1, 2020년, pp.58 - 69  

Borthakur, Madhusmita (Microbiology Laboratory, Department of Biotechnology and Bioinformatics, North-Eastern Hill University) ,  Gurung, Arun Bahadur (Computational Biology Laboratory, Department of Biotechnology and Bioinformatics, North-Eastern Hill University) ,  Bhattacharjee, Atanu (Computational Biology Laboratory, Department of Biotechnology and Bioinformatics, North-Eastern Hill University) ,  Joshi, S.R. (Microbiology Laboratory, Department of Biotechnology and Bioinformatics, North-Eastern Hill University)

Abstract AI-Helper 아이콘AI-Helper

Meghalaya, (in India), in the region of the mega-biodiversity hotspots, is home to a plethora of wild mushrooms. The present study concerns the exploration of the order Agaricales, which includes rare gilled mushrooms considered endangered under IUCN A4c criteria, due to the declining habitat. Elect...

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제안 방법

  • The protein content was found to be significantly higher. The sample was analyzed for total moisture, fiber content in its dried mass, fat content, and crude ash (Table 1). The crude protein content of the mushroom in this experiment was found to be appreciably good.
  • The findings suggest that the biogeographic features have played a unique role in determining the evolutionary traits of this fungus. The specimen was given due attention, and its ultrastructure and molecular characterization were analyzed using the Internal Transcribed Spacer (ITS) markers. However, the morphological evidence of Campanophyllum suggests an evolutionary clade in the basidiomycetes, based on the presence of the basidia.

데이터처리

  • Result considered was the mean ± SEM of 3 trials (one way ANOVA).
  • Result considered was the mean ± SEM of 3 trials (one-way ANOVA).

이론/모형

  • Folin-Ciocalteu calorimetric method was used to determine the total soluble phenolic matter of the crude extract [24]. Results were expressed in terms of mg of gallic acid equivalents per gram (mg GAE g-1 ) of the test mushroom.
  • 5 McFarland standards (106 colony forming units/mL). The antimicrobial assay was performed on Mueller Hinton Agar plates. The crude extract at a concentration of 1 mg/mL (40 mL) was used for the assay along with the pure extraction solvent (DMSO) as a negative control.
  • The mushroom sample was analyzed for its presence of nutritional composite using AOAC protocol for moisture, fat, fiber, and ash [17].
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