Production Pectinases from Some Species of Aspergillus by Solid State Fermentation and Determination of Optimum Parameters for Production: إنتاج الإنزيمات البكتينية من بعض أنواع فطور Aspergillus بطريقة تخمير الوسط الصلب وتحديد الظروف المثلى للإنتاج

Rasha Ahmad Taowz, Adib Faleh, Fateh Khateeb, Muhammad A Rasha Ahmad Taowz, Adib Faleh, Fateh Khateeb, Muha
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Abstract

After twenty Fungal isolates belong to Aspergillus Genus were obtained from sixty four samples from Fruits and Vegetables, and election the best according to its production Pectinases on solid medium. The strongest five isolates were chosen to product Pectinases by using solid state fermentation to know the ability of the elected isolates to produce pectinases, and determinate the highest enzyme production isolate, in addition to optimize the enzyme production for that isolate (incubation temperature, incubation period, pectin amount, inoculum volume, Suspension concentrations of spores, Carbon source, Nitrogen source). Four of these isolates were belong to Aspergillus niger and one of them were belong to Aspergillus fumigatus. Citrus peels were used in fermentation system as pectin resource. The pectin percentage in peels was calculated and it was 5%. The results showed that the activity of pectinases which was produced by isolates from citrus fruits is higher than the other isolates, and it was 51,52 U/ g. When the optimum parameters of production Pectinases were studied, the results showed that the highest activity of pectinases was obtained at 40°C of incubation temperature, 96 hours of incubation period, 2.5g of pectin amount in medium, 107 spore/ ml of spores concentration in fungal suspicion, 1.5 ml of indeed suspicion volume, using Citrus pectin as carbon sources, and Ammonium sulfate as nitrogen sources.
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从64份果蔬样品中分离得到20株曲霉属真菌,并根据其在固体培养基上产生的果胶酶进行筛选。选择最强的5株菌株进行固体发酵生产果胶酶,了解所选菌株生产果胶酶的能力,确定产酶能力最高的菌株,并优化该菌株的产酶能力(培养温度、培养周期、果胶量、接种量、孢子悬浮液浓度、碳源、氮源)。其中4株属于黑曲霉,1株属于烟曲霉。以柑橘果皮为原料,在发酵系统中作为果胶原料。计算果皮中果胶含量为5%。结果表明,柑橘果实分离株生产的果胶酶活性高于其他分离株,为51,52 U/ g。在研究生产果胶酶的最佳参数时,在培养温度40℃,培养时间96 h,培养基中果胶量2.5g,真菌怀疑孢子浓度107个孢子/ ml,真病菌怀疑体积1.5 ml时,果胶酶活性最高。以柑橘果胶为碳源,硫酸铵为氮源。
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