根霉2-脱氧葡萄糖抗性突变体生产原料木薯淀粉消化葡萄糖淀粉酶的研究。

Yoshiki Tani, Akira Fuji, Hiroshi Nishise
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引用次数: 25

摘要

为了提高生木薯淀粉消化糖淀粉酶根霉MB46在液体培养中的产量,获得了一株抗2-脱氧葡萄糖的突变菌株AF-1。突变菌株在0.5%葡萄糖的存在下产生葡萄糖淀粉酶,而亲本菌株则没有。在米糠液体培养基中,产量是野生型菌株的2倍以上。添加β-环糊精的米糠液体培养基对葡萄糖淀粉酶的产生也很有效。在液体培养和固体培养中,突变菌株AF-1也比野生型菌株产生更高水平的其他浸渍酶。除葡萄糖淀粉酶外,两种菌株在cm -纤维素柱层析上的洗脱模式基本相同。突变菌株AF-1的培养滤液消化10%的生木薯淀粉和木薯废料,培养60 h后葡萄糖产量为7%,培养48 h后葡萄糖产量为3.2%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Production of raw cassava starch-digestive glucoamylase by a 2-deoxyglucose-resistant mutant of Rhizopus sp.

In order to improve the productivity of raw cassava starch-digestive glucoamylase of Rhizopus sp. MB46 in a liquid culture, a mutant strain, AF-1, which is resistant to 2-deoxyglucose, was derived. The mutant strain produced glucoamylase in the presence of 0.5% glucose though the parent strain did not. With a rice bran liquid medium the productivity was over 2-times that of the wild type strain. A rice bran liquid medium supplemented with β-cyclodextrin was also effective for glucoamylase production. Other maceration enzymes were also produced at a higher level with mutant strain AF-1 than with the wild type strain in a liquid culture as well as in a solid culture. The elution patterns of these enzymes on CM-cellulose column chromatography were principally the same with both strains except for glucoamylase. When 10% of raw cassava starch and cassava waste were digested with the culture filtrate of mutant strain AF-1, glucose was produced in 7% after 60-h incubation and 3.2% after 48-h incubation, respectively.

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