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dc.contributor.authorBASUMATARY, NOYMI-
dc.date.accessioned2025-02-06T08:46:35Z-
dc.date.available2025-02-06T08:46:35Z-
dc.date.issued2024-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/355-
dc.description.abstractstudies. Methanolic and hexane solvents were used for extraction of secondary compounds. Preliminary phytochemical analysis revealed the presence of alkaloid, flavonoid, phenolic compounds, tannin and triterpenoids whereas saponin was absent in both of the extracts. Presence of the above mentioned compounds have very potent antimicrobial property. Highest phenolic content was found in methanolic extract of D. picta (112.33±0.13 mg GAE g -1 DW) followed by D. papillulifera (73.84±3.19 mg GAE g -1 DW) and highest flavonoid content was found in methanolic extract of D. papillulifera (26.54±0.67 mg QE g -1 DW) followed by D. picta (21.23±1.35 mg QE g -1 DW). For antimicrobial activity, Pyricularia oryzae (MTCC 1477), Xanthomonas oryzae (MTCC 11102), Colletotrichum gloesporoides (MTCC 10529) and Sclerotonia slerotium (MTCC 8785). were considered. This study revealed that methanolic extract of D. picta showed potential antimicrobial activity against phytopathogens of Rice and Jute crop plants viz. Pyricularia oryzae and Colletotrichum gloesporoides. The extracts were effective in inhibiting the mycelial growth of phytopathogenic fungi and the vulnerability to the extract was in the order: P. oryzae > C. gloesporoides > X. oryzae > S. slerotium. The Minimal inhibitory concentrations and IC50 values of the tested foliose lichens against tested phytopathogens. The MIC values of the methanolic extracts were lower than that of hexane extracts. In future further research on secondary metabolites of D. picta could lead to use the lichen as a potent biological control measurement as fungiside. Keywords: Lichen Biodiversity, North-East India, Endemic, New records, Phytochemical screening, Phytopathogens, Antimicrobial screening.studies. Methanolic and hexane solvents were used for extraction of secondary compounds. Preliminary phytochemical analysis revealed the presence of alkaloid, flavonoid, phenolic compounds, tannin and triterpenoids whereas saponin was absent in both of the extracts. Presence of the above mentioned compounds have very potent antimicrobial property. Highest phenolic content was found in methanolic extract of D. picta (112.33±0.13 mg GAE g -1 DW) followed by D. papillulifera (73.84±3.19 mg GAE g -1 DW) and highest flavonoid content was found in methanolic extract of D. papillulifera (26.54±0.67 mg QE g -1 DW) followed by D. picta (21.23±1.35 mg QE g -1 DW). For antimicrobial activity, Pyricularia oryzae (MTCC 1477), Xanthomonas oryzae (MTCC 11102), Colletotrichum gloesporoides (MTCC 10529) and Sclerotonia slerotium (MTCC 8785). were considered. This study revealed that methanolic extract of D. picta showed potential antimicrobial activity against phytopathogens of Rice and Jute crop plants viz. Pyricularia oryzae and Colletotrichum gloesporoides. The extracts were effective in inhibiting the mycelial growth of phytopathogenic fungi and the vulnerability to the extract was in the order: P. oryzae > C. gloesporoides > X. oryzae > S. slerotium. The Minimal inhibitory concentrations and IC50 values of the tested foliose lichens against tested phytopathogens. The MIC values of the methanolic extracts were lower than that of hexane extracts. In future further research on secondary metabolites of D. picta could lead to use the lichen as a potent biological control measurement as fungiside. Keywords: Lichen Biodiversity, North-East India, Endemic, New records, Phytochemical screening, Phytopathogens, Antimicrobial screening.studies. Methanolic and hexane solvents were used for extraction of secondary compounds. Preliminary phytochemical analysis revealed the presence of alkaloid, flavonoid, phenolic compounds, tannin and triterpenoids whereas saponin was absent in both of the extracts. Presence of the above mentioned compounds have very potent antimicrobial property. Highest phenolic content was found in methanolic extract of D. picta (112.33±0.13 mg GAE g -1 DW) followed by D. papillulifera (73.84±3.19 mg GAE g -1 DW) and highest flavonoid content was found in methanolic extract of D. papillulifera (26.54±0.67 mg QE g -1 DW) followed by D. picta (21.23±1.35 mg QE g -1 DW). For antimicrobial activity, Pyricularia oryzae (MTCC 1477), Xanthomonas oryzae (MTCC 11102), Colletotrichum gloesporoides (MTCC 10529) and Sclerotonia slerotium (MTCC 8785). were considered. This study revealed that methanolic extract of D. picta showed potential antimicrobial activity against phytopathogens of Rice and Jute crop plants viz. Pyricularia oryzae and Colletotrichum gloesporoides. The extracts were effective in inhibiting the mycelial growth of phytopathogenic fungi and the vulnerability to the extract was in the order: P. oryzae > C. gloesporoides > X. oryzae > S. slerotium. The Minimal inhibitory concentrations and IC50 values of the tested foliose lichens against tested phytopathogens. The MIC values of the methanolic extracts were lower than that of hexane extracts. In future further research on secondary metabolites of D. picta could lead to use the lichen as a potent biological control measurement as fungiside. Keywords: Lichen Biodiversity, North-East India, Endemic, New records, Phytochemical screening, Phytopathogens, Antimicrobial screening.en_US
dc.language.isoenen_US
dc.publisherDEPT OF BIOTECHNOLOGYen_US
dc.titleSTUDY ON GLUCOSE-6- PHOSPHATE DEHYDROGENASE (G6PD) VARIANTS ND IT ASSOCIATION WITH HAEMOGLOBINOPA THIES AMONG THE TRIBAL POPULATION OF MALARIA ENDEMIC INDO-BHUTAN BORDER DISTRICTS OF BTR, ASSAM, INDIAen_US
dc.typeThesisen_US
Appears in Collections:BIOTECHNOLOGY

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01_Title_page.pdf16.55 kBAdobe PDFView/Open
02_Preliminary_page.pdf1.98 MBAdobe PDFView/Open
03_Contents.pdf249.25 kBAdobe PDFView/Open
04_Abstract.pdf268.91 kBAdobe PDFView/Open
05_Chapter_1_Introduction.pdf811.09 kBAdobe PDFView/Open
06_Chapter_2_Review.pdf521.57 kBAdobe PDFView/Open
07_Chapter_3_Materials_and_method.pdf719.52 kBAdobe PDFView/Open
08_Chapter_4_Results.pdf4.17 MBAdobe PDFView/Open
09_Chapter_5_Discussion.pdf421.35 kBAdobe PDFView/Open
10_Annexure.pdf7.35 MBAdobe PDFView/Open
11_Recommendation.pdf271.52 kBAdobe PDFView/Open


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