Determination of Optimum Solid Culture Conditions for the Raw Sago Starch-Digesting Amylase Production by Penicillium brunneum.

N. Haska, Y. Ohta
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引用次数: 3

Abstract

With the present need for raw sago starch-digesting enzyme preparation, fungi obtained from sago palm tree and sago starch processing sites were screened for production of the amylase. We selected Penicillium brunneum as a source of raw starch-digesting amylase. This fungus was cultivated on a solid culture medium containing 42% wheat bran, 4% sago starch, 4% rice hull and 50% water at 30°C for 7 days. The extract of that culture was found to have ability to digest raw starch granules. Optimum solid culture conditions to produce the enzyme were studied by cultivating this strain at various incubation conditions. Optimum initial pH and optimum temperature were 4.5 and 33°C, respectively. The enzyme produced in the culture medium consisting of 56% wheat bran, 4% sago starch and 40% water, had higher raw sago starch-digestive activity. Addition of 20 mM of CaCl2 or 20 mM of NiC12 and addition of 0.02 % of yeast extract in the culture medium was effective in increasing the production of the enzyme to digest raw sago starch. The culture could be harvested after 6 days cultivation.
青霉产生西米淀粉消化淀粉酶最佳固体培养条件的确定。
鉴于目前对原料西米淀粉消化酶制备的需求,从西米棕榈树和西米淀粉加工地点获得的真菌进行了筛选,用于生产西米淀粉消化酶。我们选择青霉作为原料淀粉消化淀粉酶的来源。在含42%麦麸、4%西米淀粉、4%稻壳和50%水的固体培养基上,30℃培养7天。该培养物的提取物被发现具有消化生淀粉颗粒的能力。在不同的培养条件下对该菌株进行培养,研究了产酶的最佳固体培养条件。最佳初始pH为4.5℃,最佳温度为33℃。在56%麦麸、4%西米淀粉和40%水的培养基中产生的酶具有较高的生西米淀粉消化活性。在培养基中添加20 mM的CaCl2或20 mM的NiC12,并添加0.02%的酵母提取物,可有效提高西米淀粉消化酶的产量。培养6天后即可收获。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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