Horinouchi S, Byeon W H, Weisblum B
J Bacteriol. 1983 Jun;154(3):1252-62. doi: 10.1128/jb.154.3.1252-1262.1983.
Macrolide-lincosamide-streptogramin B resistance specified by Streptococcus sanguis plasmid pAM77 involves an adenine methylase, whose synthesis, demonstrable both phenotypically and by analysis of methionine-labeled proteins made in Bacillus subtilis minicells, is inducible by erythromycin, lincomycin, and streptogramin type B antibiotics. Localization of the methylase structural gene, including its control region in DNA fragments obtained with restriction endonucleases, has been deduced from DNA blot experiments with characterized target and probe DNAs from other streptococci, combined with DNA sequence analysis and comparison of the putative streptococcal methylase sequence with that of a cognate methylase in staphylococcal plasmid pE194. The streptococcal methylase migrates electrophoretically in polyacrylamide gels with the mobility of a 29,000-dalton protein. The sequence organization of the putative streptococcal methylase mRNA leader sequence partially resembles its staphylococcal counterpart and can support a similar mechanism of secondary structure rearrangement leading to methylase synthesis. The deduced 5' leader sequence preceding the pAM77 methylase structural gene sequence comprises approximately 155 nucleotides within which one can identify a putative control peptide 36 amino acid residues in length (in contrast to 19 in the pE194 peptide) and at least 14 possible classes of overlapping inverted complementary repeat sequences (in contrast to 3 in the pE194 control region), one of which can sequester the sequence AGGAG 7 nucleotides upstream from the putative (methionine) start codon of the streptococcal methylase. Comparison of the pAM77 and pE194 methylase amino acid sequences and their respective nucleotide sequences shows 51% conservation of amino acid residues (124 of 244) and 59% conservation of nucleotide residues (433 of 738), which suggests a common origin for the two methylase structural gene sequences. Differences in mRNA base composition associated with conserved amino acid residues occur mostly in the third nucleotide ("wobble") position of codons and may reflect adaptation of methylase genes to optimal expression in host cells with differing codon use patterns.
血链球菌质粒pAM77赋予的大环内酯-林可酰胺-链阳菌素B耐药性涉及一种腺嘌呤甲基化酶,其合成在表型上以及通过对枯草芽孢杆菌微小细胞中合成的甲硫氨酸标记蛋白进行分析均可证明,可被红霉素、林可霉素和链阳菌素B型抗生素诱导。甲基化酶结构基因的定位,包括其在限制性内切酶切割获得的DNA片段中的控制区域,已通过与来自其他链球菌的特征性靶DNA和探针DNA进行DNA印迹实验推导得出,并结合DNA序列分析以及将推测的链球菌甲基化酶序列与葡萄球菌质粒pE194中的同源甲基化酶序列进行比较。链球菌甲基化酶在聚丙烯酰胺凝胶中电泳迁移时,具有29,000道尔顿蛋白质的迁移率。推测的链球菌甲基化酶mRNA前导序列的序列组织部分类似于其葡萄球菌对应物,并且可以支持导致甲基化酶合成的二级结构重排的类似机制。pAM77甲基化酶结构基因序列之前推导的5'前导序列包含约155个核苷酸,其中可以鉴定出一个推测的控制肽,长度为36个氨基酸残基(与pE194肽中的19个相反)以及至少14种可能的重叠反向互补重复序列类别(与pE194控制区域中的3种相反),其中一种可以隔离链球菌甲基化酶推测的(甲硫氨酸)起始密码子上游7个核苷酸处的AGGAG序列。pAM77和pE194甲基化酶氨基酸序列及其各自核苷酸序列的比较显示,氨基酸残基的保守率为51%(244个中的124个),核苷酸残基的保守率为59%(738个中的433个),这表明这两个甲基化酶结构基因序列有共同起源。与保守氨基酸残基相关的mRNA碱基组成差异大多发生在密码子的第三个核苷酸(“摆动”)位置,可能反映了甲基化酶基因对在具有不同密码子使用模式的宿主细胞中实现最佳表达的适应性。