CAJ | 학술논문

人工设计合成规律成簇的间隔短回文重复( CRISPR)序列特异性引物,将从临床分离的大肠埃希菌株作为模板,采用PCR扩增方法筛选含有CRISPR系统的大肠埃希菌；利用噬菌斑法从医院未经消毒处理的污水中分离大肠埃希菌噬菌体,经过PEG沉淀的方法浓缩得到高滴度的噬菌体,再用该筛选噬菌体感染上述含有CRISPR的大肠埃希菌以筛选耐受该噬菌体的大肠埃希菌菌株。最后从70株大肠埃希菌中筛选到42株含有CRISPR序列的菌株,然后采用噬菌斑法分离到1株大肠埃希菌E. coli 147-30的裂解性噬菌体IME-EC1,在此基础上利用E. coli 147-30筛选到1株耐受噬菌体IME-EC1的大肠埃希菌菌株,命名为E. coli 147-30R1。
인공설계합성규률성족적간격단회문중복( CRISPR)서렬특이성인물,장종림상분리적대장애희균주작위모판,채용PCR확증방법사선함유CRISPR계통적대장애희균；이용서균반법종의원미경소독처리적오수중분리대장애희균서균체,경과PEG침정적방법농축득도고적도적서균체,재용해사선서균체감염상술함유CRISPR적대장애희균이사선내수해서균체적대장애희균균주。최후종70주대장애희균중사선도42주함유CRISPR서렬적균주,연후채용서균반법분리도1주대장애희균E. coli 147-30적렬해성서균체IME-EC1,재차기출상이용E. coli 147-30사선도1주내수서균체IME-EC1적대장애희균균주,명명위E. coli 147-30R1。
By using PCR method with primers specific to CRISPR sequences, clinical isolates of pathogenic Esche-richia coli strains were screened for the presence of CRISPR system. The resultant CRISPR E. coli strain was used for screening phages from hospital sewage by plaque methods. The purified phage through PEG precipitation was then used to infect the original CRISPR E. coli strain for screening of the phage-resistant E. coli strains. As a result, 42 pathogenic E. coli strains containing CRISPR were identified from 70 strains and one lytic phage IME-EC1 was i-solated. By infecting E. coli 147-30 with phage IME-EC1, a phage-resistant E. coli strain designated as 147-30R1 was identified.