Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/305839
Title: Studies on Fibrinolytic agents from endophytic fungi
Researcher: Meshram, Vineet
Guide(s): Saxena, Sanjay
Keywords: Endophytes
Thrombolytic drugs
Xylarinas
University: Thapar Institute of Engineering and Technology
Completed Date: 2017
Abstract: The 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.
Pagination: 154p.
URI: http://hdl.handle.net/10603/305839
Appears in Departments:Department of Biotechnology

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02_certificate.pdf389.89 kBAdobe PDFView/Open
03_candidates declaration.pdf440.27 kBAdobe PDFView/Open
04_acknowledgement.pdf278.79 kBAdobe PDFView/Open
05_table of contents.pdf456.24 kBAdobe PDFView/Open
06_list of tables.pdf414.65 kBAdobe PDFView/Open
07_list of figures.pdf367.19 kBAdobe PDFView/Open
08_list of symbols.pdf261.28 kBAdobe PDFView/Open
09_list of abberiviations.pdf268.28 kBAdobe PDFView/Open
10_executive summary.pdf340 kBAdobe PDFView/Open
11_chapter 1.pdf163.23 kBAdobe PDFView/Open
12_chapter 2.pdf131.67 kBAdobe PDFView/Open
13_chapter 3.pdf331.91 kBAdobe PDFView/Open
14_chapter 4.pdf319.38 kBAdobe PDFView/Open
15_chapter 5.pdf1.58 MBAdobe PDFView/Open
16_chapter 6.pdf188.52 kBAdobe PDFView/Open
17_chapter 8.pdf279.02 kBAdobe PDFView/Open
18_chapter 9.pdf248.23 kBAdobe PDFView/Open
80_recommendation.pdf301.72 kBAdobe PDFView/Open
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