Barnes Marjorie H, Butler Michelle M, Wright George E, Brown Neal C
Microbiotix Inc., 1 Innovation Drive, Worcester, MA 01605, USA.
Infect Disord Drug Targets. 2012 Oct;12(5):327-31. doi: 10.2174/187152612804142279.
DNA polymerases pol IIIC and dnaE [i.e. pol IIIE] are essential for replicative DNA synthesis in low G:C Gram-positive eubacteria. Therefore, they have strong potential as targets for development of Gram-positive-selective antibacterial agents. This work has sought to extend to dnaE the recent discovery of antimicrobial agents based on pol IIIC-specific dGTP analogs. Compound 324C, a member of the same dGTP analog family, was found to be a potent and selective inhibitor of isolated dnaE in vitro. Surprisingly, 324C had no inhibitory effect in either intact Bacillus subtilis cells or in permeabilized cell preparations used to assess replicative DNA synthesis directly. It is proposed that the failure of 324C in the intact cell is a consequence of two major factors: (i) its template-dependent base pairing mechanism, and (ii) a specific subordinate role which dnaE apparently plays to pol IIIC. To generate an effective dnaE-selective inhibitor of replicative DNA synthesis in Gram-positive bacteria, it will likely be necessary to develop a molecule that attacks the enzyme's active site directly, without binding to template DNA.
DNA聚合酶Pol IIIC和dnaE(即Pol IIIE)对于低G:C含量的革兰氏阳性真细菌中的复制性DNA合成至关重要。因此,它们作为革兰氏阳性选择性抗菌剂的开发靶点具有很大潜力。这项工作试图将基于Pol IIIC特异性dGTP类似物的抗菌剂的最新发现扩展到dnaE。化合物324C是同一dGTP类似物家族的成员,被发现是体外分离的dnaE的强效和选择性抑制剂。令人惊讶的是,324C在完整的枯草芽孢杆菌细胞或用于直接评估复制性DNA合成的透化细胞制剂中均无抑制作用。有人提出,324C在完整细胞中失效是两个主要因素的结果:(i)其模板依赖性碱基配对机制,以及(ii)dnaE显然对Pol IIIC起的特定从属作用。为了产生一种有效的革兰氏阳性细菌中复制性DNA合成的dnaE选择性抑制剂,可能有必要开发一种直接攻击该酶活性位点而不与模板DNA结合的分子。