Studies on Fibrinolytic agents from endophytic fungi

dc.contributor.guideSaxena, Sanjay
dc.coverage.spatial
dc.creator.researcherMeshram, Vineet
dc.date.accessioned2020-11-06T05:35:07Z
dc.date.available2020-11-06T05:35:07Z
dc.date.awarded
dc.date.completed2017
dc.date.registered
dc.description.abstractThe present study was oriented towards exploration of potential endophytic fungi isolated from conserved rain forests of India for their fibrinolytic activity. Of the 211 isolates of endophytic fungi screened, culture filtrates of 67 isolates exhibited in vitro proteolytic activity while only 37 isolates displayed in vitro fibrinolytic activity. However, the direct in vitro fibrinolytic activity was only found in culture filtrates of six isolates. The endophytic fungal isolate #37 CRSTBRT exhibited maximum in vitro proteolytic as well as in vitro fibrinolytic activity. Using morphological as well as molecular taxonomic studies, #37 CRSTBRT was identified as Xylaria curta. The fibrinolytic moiety expressed in the culture filtrate of Xylaria curta was isolated using chromatographic techniques. Further, its purity, molecular mass and enzymatic activity was ascertained by using electrophoretic techniques, HPLC and MALDI ToF MS analysis. Xylarinase is a non toxic, bi functional monomeric fibrinolytic metalloprotease with a molecular mass of 33.76 kDa. The enzyme displayed both plasmin like and plasminogen activator like activity under in vitro conditions. It hydrolyses both Aand#945; and Band#946; chains of fibrin(ogen) displaying and#945;and#946; fibrinogenase activity. Optimal fibrinolytic activity of xylarinase was observed at 35 °C, pH 8. EDTA and EGTA were the potent inhibitors of xylarinase suggesting that the enzyme was a metalloprotease having calcium dependence. However, Fe2+ and Zn2+ strongly inhibited the in vitro fibrinolytic activity of xylarinase. The Km and Vmax of xylarinase was 246 µM and 1.22 µM/min. The N-terminal sequence of xylarinase (SNGPLPGGVVWAG) did not show any homology with previously known fibrinolytic enzymes. Further, xylarinase was found to prolong the APTT and PT. Xylarinase exhibited no cytotoxic effect over RAW 264.7 murine macrophage cell. The production yield of xylarinase was enhanced (8.5 % from 0.09 %) by producing it on rice chaff using solid state fermentation.
dc.description.note
dc.format.accompanyingmaterialNone
dc.format.dimensions
dc.format.extent154p.
dc.identifier.urihttp://hdl.handle.net/10603/305839
dc.languageEnglish
dc.publisher.institutionDepartment of Biotechnology
dc.publisher.placePatiala
dc.publisher.universityThapar Institute of Engineering and Technology
dc.relation
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordEndophytes
dc.subject.keywordThrombolytic drugs
dc.subject.keywordXylarinas
dc.titleStudies on Fibrinolytic agents from endophytic fungi
dc.title.alternative
dc.type.degreePh.D.

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