Cheng C W, Yang S S
Department of Agricultural Chemistry, National Taiwan University, Taipei, Republic of China.
Zhonghua Min Guo Wei Sheng Wu Ji Mian Yi Xue Za Zhi. 1995 May;28(2):109-16.
Streptomyces rimosus TM-55 was treated with 3% ethyl melthylsulfonate for 60 minutes to generate mutants producing high amount of amylase, and 1,283 mutants were isolated from yeast extract starch (YS) medium containing 0.1% 2-deoxyglucose. Amylase activity was primarily screened by clear zone formation on YS medium after spraying with iodine solution. Two mutants designed as D-35 and D-62 had higher amylase activity than that of the parent strain. Amylase activity of the mutants in the YS broth was 2.97- and 3.45-fold of the parent strain, respectively. With the addition of 0.1% lactose, and 2-deoxyglucose, amylase activity of the mutants D-35 and D-62 was 27-73% and 4-7% higher than that of the parent strain. With the addition of 0.1% sucrose, amylase activity of the mutant D-35 was 18.37% lower than that of the parent strain. Moreover, with the supplement of 0.1% glucose, amylase activity of both the mutants D-35 and D-62 was 3.67 and 3.40 fold of the parent strain.
用3%的甲基磺酸乙酯处理龟裂链霉菌TM - 55 60分钟,以产生大量淀粉酶的突变体,并从含有0.1% 2 - 脱氧葡萄糖的酵母提取物淀粉(YS)培养基中分离出1283个突变体。淀粉酶活性主要通过在喷洒碘溶液后在YS培养基上形成透明圈来初步筛选。两个被设计为D - 35和D - 62的突变体具有比亲本菌株更高的淀粉酶活性。突变体在YS肉汤中的淀粉酶活性分别是亲本菌株的2.97倍和3.45倍。添加0.1%乳糖和2 - 脱氧葡萄糖后,突变体D - 35和D - 62的淀粉酶活性分别比亲本菌株高27 - 73%和4 - 7%。添加0.1%蔗糖后,突变体D - 35的淀粉酶活性比亲本菌株低18.37%。此外,添加0.1%葡萄糖后,突变体D - 35和D - 62的淀粉酶活性分别是亲本菌株的3.67倍和3.40倍。