Lázaro E, Sanz E, Remacha M, Ballesta J P G
Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas y Universidad Autónoma de Madrid, Canto Blanco, 28049 Madrid, Spain.
Antimicrob Agents Chemother. 2002 Sep;46(9):2914-9. doi: 10.1128/AAC.46.9.2914-2919.2002.
The antitumor antibiotic sparsomycin, produced by Streptomyces sparsogenes, is a universal translation inhibitor that blocks the peptide bond formation in ribosomes from all species. Sparsomycin-resistant strains were selected by transforming the sensitive Streptomyces lividans with an S. sparsogenes library. Resistance was linked to the presence of a plasmid containing an S. sparsogenes 5.9-kbp DNA insert. A restriction analysis of the insert traced down the resistance to a 3.6-kbp DNA fragment, which was sequenced. The analysis of the fragment nucleotide sequence together with the previous restriction data associate the resistance to srd, an open reading frame of 1,800 nucleotides. Ribosomes from S. sparsogenes and the S. lividans-resistant strains are equally sensitive to the inhibitor and bind the drug with similar affinity. Moreover, the drug was not modified by the resistant strains. However, resistant cells accumulated less antibiotic than the sensitive ones. In addition, membrane fractions from the resistant strains showed a higher capacity for binding the drug. The results indicate that resistance in the producer strain is not connected to either ribosome modification or drug inactivation, but it might be related to an alteration in the sparsomycin permeability barrier.
由稀疏链霉菌产生的抗肿瘤抗生素稀疏霉素是一种通用的翻译抑制剂,可阻断所有物种核糖体中的肽键形成。通过用稀疏链霉菌文库转化敏感的变铅青链霉菌来筛选对稀疏霉素耐药的菌株。耐药性与含有稀疏链霉菌5.9kbp DNA插入片段的质粒的存在有关。对该插入片段的限制性分析将耐药性追溯到一个3.6kbp的DNA片段,并对其进行了测序。对该片段核苷酸序列的分析以及先前的限制性数据表明,耐药性与srd有关,srd是一个1800个核苷酸的开放阅读框。稀疏链霉菌和变铅青链霉菌耐药菌株的核糖体对该抑制剂同样敏感,且以相似的亲和力结合药物。此外,耐药菌株并未对药物进行修饰。然而,耐药细胞积累的抗生素比敏感细胞少。另外,耐药菌株的膜组分显示出更高的结合药物的能力。结果表明,产生菌中的耐药性既不与核糖体修饰有关,也不与药物失活有关,但可能与稀疏霉素渗透屏障的改变有关。