Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/448689
Title: Production Immobilization and Characterization of Fungal Phytase and its Utilization in Food and Feed Industry
Researcher: Kumari, Neha
Guide(s): Bansal, Saurabh
Keywords: Biotechnology and Applied Microbiology
Life Sciences
Microbiology
Nanoparticles
Phytases
Solid-state fermentation
Zinc oxide
University: Jaypee University of Information Technology, Solan
Completed Date: 2022
Abstract: The phytases hydrolyze the phytic acid to release the bound phosphorus and other vital nutrients in the feed of domestic animals, plummeting the requirement for extra subjection to feed. However, its short half-life owing to less stability and the high production cost due to the unavailability of cheaper sources for phytase production limited its application in developing countries. Also, fewer studies have been reported on phytases usage in humans. The use of phytase as a food additive can overcome the issue of malnutrition and silent hunger in developing countries. Besides this, using phytase in the animal feed not only reduces the cost of the livestock industry but also deals with the concern of phosphorus pollution (eutrophication) up to a level. Therefore, in the current study, a fungal culture, Aspergillus niger NT7, was isolated from the soil sample of the agriculture field and identified as a potential phytase producer. The A. niger NT7 phytase production was done using an economical substrate, wheat bran, an agricultural waste, via solid-state fermentation (SSF). The enhanced phytase production was obtained through optimizing different physiochemical parameters by two approaches; one variable at a time (OVAT) and statistical Response Surface Methodology (RSM). The optimized parameters obtained by the OVAT are the moistening agent (distilled water), inoculum age (3-days) and level (15×107 spores/ml), pH (5.0), temperature (30 °C) and different supplements of biochemical such as nitrogen (ammonium sulphate), sugar (mannitol), phosphorous (potassium dihydrogen phosphate) and detergent (Tween 80) source. The optimization procedures through OVAT (208 ± 0.22 U/gds) enhanced the overall output by around 2.7-fold compared to unoptimized culture conditions (76.34 ± 0.99 U/gds). newline
Pagination: xxix,196p.
URI: http://hdl.handle.net/10603/448689
Appears in Departments:Department of Biotechnology

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02_prelim pages.pdf1.77 MBAdobe PDFView/Open
03_content.pdf407.73 kBAdobe PDFView/Open
04_abstract.pdf255.86 kBAdobe PDFView/Open
05_chapter 1.pdf349.3 kBAdobe PDFView/Open
06_chapter 2.pdf1.28 MBAdobe PDFView/Open
07_chapter 3.pdf920.59 kBAdobe PDFView/Open
08_chapter 4.pdf1.18 MBAdobe PDFView/Open
09_chapter 5.pdf1.67 MBAdobe PDFView/Open
10_chapter 6.pdf1.13 MBAdobe PDFView/Open
11_annexures.pdf1.96 MBAdobe PDFView/Open
80_recommendation.pdf706.89 kBAdobe PDFView/Open
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