The Bacillus strains preserved in our laboratory was used as the original strain to be mutated using UV mutagenesis and diethyl sulfate in order to increase the production of amylase. A mutant strain which was stable in hereditary was obtained. The results indicated that the strain of D-2 had a high production of amylase. The yield of amylase reached 6.599U/ml, which was 4 folds higher than that of the starting strain. A new efficient starch-hydrolysis enzyme strain screening method was developed, which made a good foundation for further medium optimization.%该研究以实验室保存的枯草芽孢杆菌为出发菌株,利用紫外和硫酸二乙酯(DES)复合诱变的方法,从大量突变菌株中获取可高效发酵生产淀粉酶的菌株.又通过连续传代实验,确定了该突变菌株突变性状能稳定遗传.结果表明,菌株D-2具有较高的的淀粉酶活力,其淀粉酶活力可达到6.599U/mL,较出发菌株提高到4倍.并在连续培养5代后,仍具有较好的遗传稳定性.该文探讨了一种高效的发酵生产淀粉酶菌株的选育方法,为下一步菌种生长条件优化打下了基础.
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