Schüller Anna, Matzner Daniel, Lünse Christina E, Wittmann Valentin, Schumacher Catherine, Unsleber Sandra, Brötz-Oesterhelt Heike, Mayer Christoph, Bierbaum Gabriele, Mayer Günter
University of Bonn, LIMES Institute, Gerhard-Domagk-Strasse 1, 53121, Bonn, Germany.
University of Leipzig, Institute for Biochemistry, Brüderstrasse 34, 04103, Leipzig, Germany.
Chembiochem. 2017 Mar 2;18(5):435-440. doi: 10.1002/cbic.201600491. Epub 2017 Jan 30.
The ever-growing number of pathogenic bacteria resistant to treatment with antibiotics call for the development of novel compounds with as-yet unexplored modes of action. Here, we demonstrate the in vivo antibacterial activity of carba-α-d-glucosamine (CGlcN). In this mode of action study, we provide evidence that CGlcN-mediated growth inhibition is due to glmS ribozyme activation, and we demonstrate that CGlcN hijacks an endogenous activation pathway, hence utilizing a prodrug mechanism. This is the first report describing antibacterial activity mediated by activating the self-cleaving properties of a ribozyme. Our results open the path towards a compound class with an entirely novel and distinct molecular mechanism.
对抗生素治疗产生耐药性的致病细菌数量不断增加,这就需要开发具有尚未探索作用方式的新型化合物。在此,我们展示了碳青霉烯-α-D-葡萄糖胺(CGlcN)的体内抗菌活性。在这项作用方式研究中,我们提供证据表明CGlcN介导的生长抑制是由于glmS核酶激活,并且我们证明CGlcN劫持了内源性激活途径,从而利用了前药机制。这是第一份描述通过激活核酶的自我切割特性介导的抗菌活性的报告。我们的结果为具有全新且独特分子机制的一类化合物开辟了道路。