Characterization of a starch-hydrolyzing α-amylase produced by Aspergillus niger WLB42 mutated by ethyl methanesulfonate treatment.

International journal of biochemistry and molecular biology Pub Date : 2016-06-01 eCollection Date: 2016-01-01
Shihui Wang, Chaoyang Lin, Yun Liu, Zhicheng Shen, Jenasia Jeyaseelan, Wensheng Qin
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Abstract

Aspergillus niger is the most commonly used fungus for commercial amylase production, the increase of amylase activity will be beneficial to the amylase industry. Herein we report a high α-amylase producing (HAP) A. niger WLB42 mutated from A. niger A4 by ethyl methanesulfonate treatment. The fermentation conditions for the amylase production were optimized. The results showed that both the amylase activity and total protein content reached highest after 48-h incubation in liquid medium using starch as the sole carbon source. The enzyme production reached maximum at temperature of 30°C, pH 7, with 40 g/L starch in the medium inoculated with 1.4% v/v spore. When 0.3% w/v urea was added to the liquid medium as a nitrogen source, the amylase activity was elevated by 20%. Nine monosaccharides and derivatives were tested for α-amylase induction, glucose was the best inducer. Furthermore, the enzymology characterization of amylase was conducted. The molecular weight of amylase was determined to be 50 kD by SDS-PAGE. The amylase had maximum activity at 45°C and pH 7. The activity could be dramatically triggered by adding 1 mM Co(2+), increased to 250%. The activity was inhibited by detergents SDS and Triton X-100. Six different brands of starch were tested for amylase activity, the results demonstrated that the more soluble of the starch, the higher hydrolyzability of the substrate by amylase.

Abstract Image

甲磺酸乙酯诱变黑曲霉WLB42产生的淀粉水解α-淀粉酶的特性
黑曲霉是商业生产淀粉酶最常用的真菌,淀粉酶活性的提高将有利于淀粉酶工业的发展。在此,我们报道了一种高α-淀粉酶(HAP)黑木耳WLB42通过甲磺酸乙酯处理从黑木耳A4中突变而来。优化了生产淀粉酶的发酵条件。结果表明,以淀粉为唯一碳源,在液体培养基中培养48 h后,淀粉酶活性和总蛋白含量均达到最高。在温度为30℃,pH为7,淀粉含量为40 g/L的培养基中接种1.4% v/v的孢子,产酶量达到最大。在液体培养基中添加0.3% w/v尿素作为氮源,淀粉酶活性提高20%。9种单糖及其衍生物对α-淀粉酶的诱导作用,以葡萄糖为最佳诱导剂。并对淀粉酶进行了酶学表征。SDS-PAGE测定淀粉酶分子量为50 kD。淀粉酶在45℃、pH为7时活性最高。添加1 mM Co(2+)可显著激活活性,使其增加到250%。SDS和Triton X-100对活性有抑制作用。对6种不同牌号的淀粉进行了淀粉酶活性测试,结果表明,淀粉的可溶性越高,淀粉酶对底物的水解能力越高。
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