Kovalic D, Giannattasio R B, Jin H J, Weisblum B
Department of Pharmacology, University of Wisconsin Medical School, Madison 53706.
J Bacteriol. 1994 Nov;176(22):6992-8. doi: 10.1128/jb.176.22.6992-6998.1994.
The DNA sequence that encodes 23S rRNA domain V of Bacillus subtilis, nucleotides 2036 to 2672 (C. J. Green, G. C. Stewart, M. A. Hollis, B. S. Vold, and K. F. Bott, Gene 37:261-266, 1985), was cloned and used as a template from which to transcribe defined domain V RNA in vitro. The RNA transcripts served as a substrate in vitro for specific methylation of B. subtilis adenine 2085 (adenine 2058 in Escherichia coli 23S rRNA) by the ErmSF methyltransferase, an enzyme that confers resistance to the macrolide-lincosamide-streptogramin B group of antibiotics on Streptomyces fradiae NRRL 2702, the host from which it was cloned. Thus, neither RNA sequences belonging to domains other than V nor the association of 23S rRNA with ribosomal proteins is needed for the specific methylation of adenine that confers resistance to the macrolide-lincosamide-streptogramin B group of antibiotics.
编码枯草芽孢杆菌23S rRNA结构域V的DNA序列(核苷酸2036至2672,C. J. 格林、G. C. 斯图尔特、M. A. 霍利斯、B. S. 沃尔德和K. F. 博特,《基因》37:261 - 266,1985年)被克隆,并用作体外转录特定结构域V RNA的模板。RNA转录本在体外作为底物,用于ErmSF甲基转移酶对枯草芽孢杆菌腺嘌呤2085(大肠杆菌23S rRNA中的腺嘌呤2058)进行特异性甲基化,该酶赋予从其克隆的宿主弗氏链霉菌NRRL 2702对大环内酯 - 林可酰胺 - 链阳霉素B组抗生素的抗性。因此,赋予对大环内酯 - 林可酰胺 - 链阳霉素B组抗生素抗性的腺嘌呤特异性甲基化既不需要属于V结构域以外的RNA序列,也不需要23S rRNA与核糖体蛋白的结合。