Sudarsan Narasimhan, Cohen-Chalamish Smadar, Nakamura Shingo, Emilsson Gail Mitchell, Breaker Ronald R
Department of Molecular, Cellular and Developmental Biology, Yale University, P.O. Box 208103, New Haven, Connecticut 06520, USA.
Chem Biol. 2005 Dec;12(12):1325-35. doi: 10.1016/j.chembiol.2005.10.007.
Thiamine metabolism genes are regulated in numerous bacteria by a riboswitch class that binds the coenzyme thiamine pyrophosphate (TPP). We demonstrate that the antimicrobial action of the thiamine analog pyrithiamine (PT) is mediated by interaction with TPP riboswitches in bacteria and fungi. For example, pyrithiamine pyrophosphate (PTPP) binds the TPP riboswitch controlling the tenA operon in Bacillus subtilis. Expression of a TPP riboswitch-regulated reporter gene is reduced in transgenic B. subtilis or Escherichia coli when grown in the presence of thiamine or PT, while mutant riboswitches in these organisms are unresponsive to these ligands. Bacteria selected for PT resistance bear specific mutations that disrupt ligand binding to TPP riboswitches and derepress certain TPP metabolic genes. Our findings demonstrate that riboswitches can serve as antimicrobial drug targets and expand our understanding of thiamine metabolism in bacteria.
硫胺素代谢基因在许多细菌中受一类核糖开关调控,这类核糖开关可结合辅酶硫胺素焦磷酸(TPP)。我们证明,硫胺素类似物吡硫胺(PT)的抗菌作用是通过与细菌和真菌中的TPP核糖开关相互作用介导的。例如,吡硫胺焦磷酸(PTPP)可结合控制枯草芽孢杆菌tenA操纵子的TPP核糖开关。在硫胺素或PT存在的情况下生长时,转基因枯草芽孢杆菌或大肠杆菌中TPP核糖开关调控的报告基因的表达会降低,而这些生物体中的突变核糖开关对这些配体无反应。选择对PT具有抗性的细菌带有特定突变,这些突变会破坏配体与TPP核糖开关的结合,并使某些TPP代谢基因去阻遏。我们的研究结果表明,核糖开关可作为抗菌药物靶点,并扩展了我们对细菌中硫胺素代谢的理解。