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العنوان
Production and characterization of selective fungal tannase /
الناشر
Hebat-Allah Abdallah Salem ,
المؤلف
Hebat Allah Abdallah Salem
هيئة الاعداد
باحث / Hebat Allah Abdallah Salem
مشرف / Magdy Ali Amin
مشرف / Heba A. Elrefai
مناقش / Heba A. Elrefai
تاريخ النشر
2017
عدد الصفحات
136 P. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
الصيدلة ، علم السموم والصيدلانيات (المتنوعة)
تاريخ الإجازة
26/6/2018
مكان الإجازة
جامعة القاهرة - كلية الصيدلة - Microbiology and Immunology
الفهرس
Only 14 pages are availabe for public view

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from 158

Abstract

A survey of three isolated fungal strains was carried out for the production of fungal tannases. Mucor cercinilloides isolate F6-3-12 was the strain with the highest tannase activity. Tannase enzyme was produced by Mucor circinilloides isolate utilizing different agricultural plants: Green tea leaves, sumac leaves and pomegranate rind under solid state fermentation technique and green tea or tannic acid under submerged fermentation technique. The highest tannase production was obtained by solid state fermentation in the following order pomegranate rind > green tea leaves and sumac leaves. Enhancement of tannase production was achieved by two statistically based experimental designs to optimize the fermentation medium. The plackett-burman multifactorial design was first employed to investigate the effect of 7 factors of tannase production. The most significant factors found to be moisture level, incubation period and sodium nitrate concentration. Further optimization was done using Box-Behnken design in which the effect of the three factors in three levels could be tested. The Box-Behnken design showed that the maximum yield of tannase was produced when the concentration of sodium nitrate was 8g/l with moisture level 1:6 with three days of incubation. Under optimal conditions enzyme production was increased by 5.91 fold compared to non optimized medium. The crude Mucor circinilloides isolate F6-3-12 was partially purified by precipitation with solvent at concentration 75%. The best way for partial purification was by acetone 75% in which 65.8% and 49.9% of the total activity and protein were recovered respectively