Appleyard Antony N, Choi Shaila, Read Daniel M, Lightfoot Ann, Boakes Steven, Hoffmann Anja, Chopra Ian, Bierbaum Gabriele, Rudd Brian A M, Dawson Michael J, Cortes Jesus
Novacta Biosystems Ltd., Welwyn Garden City, Hertfordshire, UK.
Chem Biol. 2009 May 29;16(5):490-8. doi: 10.1016/j.chembiol.2009.03.011.
Mersacidin is a tetracyclic lantibiotic with antibacterial activity against Gram-positive pathogens. To probe the specificity of the biosynthetic pathway of mersacidin and obtain analogs with improved antibacterial activity, an efficient system for generating variants of this lantibiotic was developed. A saturation mutagenesis library of the residues of mersacidin not involved in cycle formation was constructed and used to validate this system. Mersacidin analogs were obtained in good yield in approximately 35% of the cases, producing a collection of 82 new compounds. This system was also used for the production of deletion and insertion mutants of mersacidin. The outcome of these studies suggests that this system can be extended to produce mersacidin variants with multiple changes that will allow a full investigation of the potential use of modified mersacidins as therapeutic agents.
默那菌素是一种四环羊毛硫抗生素,对革兰氏阳性病原体具有抗菌活性。为了探究默那菌素生物合成途径的特异性并获得具有改善抗菌活性的类似物,开发了一种用于产生这种羊毛硫抗生素变体的高效系统。构建了默那菌素中不参与环形成的残基的饱和诱变文库,并用于验证该系统。在大约35%的情况下,以良好的产率获得了默那菌素类似物,产生了82种新化合物的集合。该系统还用于生产默那菌素的缺失和插入突变体。这些研究结果表明,该系统可以扩展以产生具有多种变化的默那菌素变体,这将允许全面研究修饰的默那菌素作为治疗剂的潜在用途。