镧系元素
饱和突变
突变
生物
突变体
计算生物学
生物化学
细菌
组合化学
遗传学
化学
乳酸链球菌素
基因
作者
Antony N. Appleyard,Shaila Choi,Daniel M. Read,Ann Lightfoot,Steven Boakes,Anja Hoffmann,Ian Chopra,Gabriele Bierbaum,Brian A.M. Rudd,Michael J. Dawson,Jesús Cortés
出处
期刊:Chemistry & Biology
[Elsevier BV]
日期:2009-05-01
卷期号:16 (5): 490-498
被引量:97
标识
DOI:10.1016/j.chembiol.2009.03.011
摘要
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.
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