摘要
从22份土样中,分离得到6株β-葡聚糖酶[EC.3.2.1.73]产生菌,经鉴定为枯草芽孢杆菌。以其中2株产酶活性较高的(61和55U/ml),为出发株,用NTG诱变处理,最后得到突变株CW-06。通过优化发酵培养基和发酵条件,使其产酶能力达到160U/ml以上。
Two strains of Bacillus subrilis which produce β-glucanase respectively with 61 and 55U/ml were isolated from 22 soil samples.The strains were mutated by NTG and a mutant strain CW-06 was obtained.The optimal fermentation conditions of this mutant was got by orthogonal design.In this way the β-glucanase produced by CW-06 in the broth was found more than 160 U/ml.
出处
《中国医药工业杂志》
CSCD
北大核心
1994年第8期337-339,共3页
Chinese Journal of Pharmaceuticals
关键词
葡聚糖酶
突变株
筛选
选育
β-glucanase
mutant
screening
breeding