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Optimization of gluco-amylase production from Aspergillus spp. for its use in saccharification of liquefied corn starch

机译:优化了曲霉属的葡糖淀粉酶的生产。用于糖化玉米淀粉的糖化

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摘要

Fungal gluco-amylase is required for the production of sugars from starchy substrates. Commercially available fungal gluco-amylase is quite costly which makes the process uneconomical. This study was undertaken to standardize physico-chemical parameters for optimum production of gluco-amylases from Aspergillus spp. Two fungal cultures, i.e., Aspergillus niger and Aspergillus terreus, were compared for gluco-amylase activity both under stationary and shake flask conditions. Among two fungal cultures, maximum gluco-amylase activity was shown by A. niger (243.09 U/ml) under stationary conditions as compared to A. terreus (126.34 U/ml). Gluco-amylase activity of A. niger increases by 42.48% from 243.09 to 346.35 U/ml after optimization using response surface methodology, whereby a substrate concentration of 7%, yeast extract 0.25%, temperature 32.5 °C and pH 5.5 were found to be optimum for gluco-amylase production. Crude enzyme was compared with commercial enzyme and it was found that when 500 U of Glucoamylase ex. Rhizopus were inoculated into starch-supplemented minimal media (SSMM) liquefied using 2 g of fungal diastase, it increases the reducing sugar concentration from 2.19 to 21.15 mg/ml and a saccharification efficiency of 77.7% was achieved, whereas 1.5 ml of crude enzyme (extracted from A. niger) was able to produce 14.46 mg/ml of reducing sugars with a saccharification efficiency of 53.2%.
机译:从淀粉底物生产糖需要真菌葡糖淀粉酶。商业上可获得的真菌葡糖淀粉酶非常昂贵,这使得该方法不经济。进行这项研究是为了使物理化学参数标准化,以便从曲霉属植物中最佳生产葡糖淀粉酶。比较两种真菌培养物,即黑曲霉和土曲霉,在固定和摇瓶条件下的葡糖淀粉酶活性。在两种真菌培养物中,黑曲霉(A.niger)(243.09 U / ml)在固定条件下显示的最大葡糖淀粉酶活性高于土曲霉(​​126.34 U / ml)。使用响应面方法进行优化后,黑曲霉的葡糖淀粉酶活性从243.09增加到346.35 U / ml,增加了42.48%,其中底物浓度为7%,酵母提取物为0.25%,温度为32.5°C,pH为5.5最适合生产葡萄糖淀粉酶。将粗酶与市售酶进行比较,发现当500U的葡糖淀粉酶存在时。将根霉菌接种到使用2 g真菌淀粉酶液化的补充淀粉的基本培养基(SSMM)中,将还原糖浓度从2.19毫克/毫升增加到21.15 mg / ml,糖化效率达到77.7%,而1.5毫升粗酶(提取自黑曲霉)能够产生14.46 mg / ml的还原糖,糖化效率为53.2%。

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