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机构地区:[1]中国科学院遗传研究所
出 处:《Acta Genetica Sinica》1996年第2期158-162,共5页
基 金:国家自然科学基金;中国科学院<八.五>重点科研资助
摘 要:本文利用PCR方法克隆了E.coliT83依赖链霉素(sterptomyeindependent,Sm^d)菌株中编码突变的核糖体蛋白质S12的rpsL^d基因,并进行了DNA序列分析,发现第42位密码子由编码赖氨酸(Lys,K)的AAA变为编码谷氨酰胺(Gln,Q)的CAA。依据Garnier原理预测了突变对S12蛋白质二级结构形成趋势的影响,结果表明。Using the polymerase chain reaction(PCR)method, the rpsL ̄d gene was amplified and cloned,which encodes the streptomycin-dependent(Sm ̄d)mutant of ribosomal protein S12 in E.coli T83.The result of DNA sequencing showed an AAA to CAA mutation at codon 42,leading to the substitution of glutamine(Gln,Q)for lysine(Lys,K).According to the principle of Garnier,we predicted that there might be alterations in the secondary structural propensity of protein S12 due to the mutation. The outcome indicated that the β-turn propensity at position 42 and its nearby region was increased evidently and the relative position of relevant subdomains were changed. As a result,the special conformation of the whole protein S12 was influenced.In view of that ribosomal proteins and ribosomal RNAs(rRNA)mutually adapted in structures and functions,the probable molecular mechanism.That how protein S12 Smdmutant in E.coli T83 suppressed λN gene's expression is discussed.
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