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首页> 外文期刊>Asian Journal of Microbiology, Biotechnology and Environmental Science >OPTIMIZATION AND COMPARATIVE STUDIES OF AMYLASE PRODUCTION BY IMMOBILISED BACILLUS SUBTILIS AND BACILLUS COAGULANS
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OPTIMIZATION AND COMPARATIVE STUDIES OF AMYLASE PRODUCTION BY IMMOBILISED BACILLUS SUBTILIS AND BACILLUS COAGULANS

机译:固定化芽孢杆菌和芽孢杆菌的淀粉酶生产淀粉酶的优化和比较研究

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The wide applications of amylase enzymes especially in the starch processing industries and the textile industries has made it an enzyme with a high demand a amylase production was parried out with sodium alginate immobilized Bacillus subtilis and Bacillus coagulans. The organisms are non pathogenic, produce no known toxins and have a well established record of safety. The identification of amylase producing capability of these microorganisms can be easily performed by the preliminary screening technique using starch agar. Also the methods of enrichment and assay are relatively simple as described. Calcium chloride was also provided in the production medium, as the presence of calcium ions is very much necessary for the maintenance of the stabilityof the enzyme. The maintenance of favorable pH is very essential for amylase production. Maximum activity of the enzyme was obtained at the pH of 7. acidic conditions do not favor the production of amylase. The presence of the inducer (starch) is also acritical factor in amylase production. An inducer concentration of 0.02 to 0.03 % is generally favoured for amylase production. The inducer acts as the genetic level. A longer incubation time was found to increase the activity of the enzyme. Highest production was reported after 24 hours as compard to lesser incubation times. This could be due to secretion of the extracellular enzyme after an initial growth phase of the organism. Both the organisms. Bacillus subtilis and Bacillus coagulans produced almost similar amounts of enzyme under various conditions. This also proves that Bacillus coagulans can indeed be a substitute for the widely used Bacillus subtilis.
机译:淀粉酶的广泛应用,特别是在淀粉加工工业和纺织工业中,使其成为一种需求量很高的酶,而用固定化藻酸钠的枯草芽孢杆菌和凝结芽孢杆菌可以抑制淀粉酶的生产。该生物体无致病性,不产生任何已知毒素,并具有完善的安全记录。这些微生物的淀粉酶生产能力的鉴定可以通过使用淀粉琼脂的初步筛选技术容易地进行。如上所述,富集和测定的方法也相对简单。生产介质中还提供了氯化钙,因为钙离子的存在对于维持酶的稳定性非常必要。维持合适的pH值对于淀粉酶的生产非常重要。在7的pH值下获得了最大的酶活性。酸性条件不利于淀粉酶的产生。诱导剂(淀粉)的存在也是淀粉酶生产中的关键因素。通常优选0.02至0.03%的诱导剂浓度用于淀粉酶生产。诱导物充当遗传水平。发现更长的孵育时间可以增加酶的活性。据报道,孵育时间较短,因此在24小时后产量最高。这可能是由于生物体初始生长阶段后细胞外酶的分泌。两种生物。枯草芽孢杆菌和凝结芽孢杆菌在各种条件下产生的酶量几乎相似。这也证明凝结芽孢杆菌确实可以替代广泛使用的枯草芽孢杆菌。

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