大肠杆菌
溶解
突变
细菌
基因
化学
核苷酸
细菌病毒
微生物学
噬菌体
生物
分子生物学
遗传学
生物化学
作者
Hongliang Dong,Xiangan Han,Hao Bai,Liange He,Lei Liu,Rui Liu,Tongjie Chai,Chan Ding,Haiwen Liu,Shengqing Yu
出处
期刊:PubMed
日期:2012-12-01
卷期号:28 (12): 1423-30
被引量:5
摘要
Bacterial ghost is intact envelope of Gram-negative bacteria, which is produced by the function of the lysis gene E from bacteriophage PhiX174. The expression of the lysis gene E is usually controlled by the thermosensitive lambdapL/pR-cI857 promoter. In this study, we described a mutation (T --> C) at the ninth nucleotide of the OR2 in the lambdapR promoter of the lambdapL/pR-cI857 system by overlap PCR. The bacteriolytic assay showed that the mutation in the lambdapL/pR-cI857 system enhanced the temperature of repressing the expression of gene E up to 37 degrees C. The lysis efficiency of altered lambdapR promoter in Escherichia coli DH5a and avian pathogenic E. coli DE17 was up to 99.9%. The expanded range of temperature will benefit for the production of bacterial ghost.
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