Goldberg S L, Romero J G, Deo Y M
Department of Microbiological and Cell Culture Development, Schering Corporation, Union, NJ 07083.
J Antibiot (Tokyo). 1990 Aug;43(8):992-9. doi: 10.7164/antibiotics.43.992.
We cloned DNA fragments of sisomicin-producing Micromonospora inyoensis into Streptomyces plasmid vectors and identified Streptomyces lividans TK24 transformants expressing the M. inyoensis sisomicin-resistance (sisA) gene. The sisA gene was compared to the previously reported Micromonospora purpurea Kan-Gen (kanamycin-gentamicin)-resistance gene. While the restriction endonuclease digestion patterns of the two determinants appear to be divergent, the genes are nonetheless closely related, based on similar patterns and levels of aminoglycoside-resistance and their ability to cross-hybridize under stringent conditions. We have transformed recombinant plasmid pMD5-2, which carries the sisA gene, into our M. purpurea gentamicin-production strain and determined that gentamicin biosynthesis was not improved.
我们将产生紫苏霉素的英约小单孢菌(Micromonospora inyoensis)的DNA片段克隆到链霉菌质粒载体中,并鉴定出表达英约小单孢菌紫苏霉素抗性(sisA)基因的变铅青链霉菌(Streptomyces lividans)TK24转化子。将sisA基因与先前报道的紫色小单孢菌(Micromonospora purpurea)Kan-Gen(卡那霉素-庆大霉素)抗性基因进行了比较。虽然这两个决定簇的限制性内切酶消化模式似乎不同,但基于相似的氨基糖苷抗性模式和水平以及它们在严格条件下交叉杂交的能力,这两个基因仍然密切相关。我们已将携带sisA基因的重组质粒pMD5-2转化到我们的紫色小单孢菌庆大霉素生产菌株中,并确定庆大霉素生物合成没有得到改善。