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bacterial proteinases as targets for the development of second-generation antibiotics

机译:细菌蛋白酶作为第二代抗生素开发的目标

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The emergence of bacterial pathogen resistance to common antibiotics strongly supports the necessity to develop alternative mechanisms for combating drug-resistant forms of these infective organisms. Currently, few pharmaceutical companies have attempted to investigate the possibility of interrupting metabolic pathways other than those that are known to be involved in cell wall biosynthesis. In this review, we describe multiple, novel roles for bacterial proteinases during infection using, as a specific example, the enzymes from the organism Porphyromonas gingivalis, a periodontopathogen, which is known to be involved in the development and progression of periodontal disease. In this manner, we are able to justify the concept of developing synthetic inhibitors against members of this class of enzymes as potential second-generation antibiotics. Such compounds could not only prove valuable in retarding the growth and proliferation of bacterial pathogens but also lead to the use of this class of inhibitors against invasion by other infective organisms.
机译:细菌对普通抗生素的病原体抗药性的出现强烈支持开发对抗这些感染性生物体耐药形式的替代机制的必要性。目前,除了已知与细胞壁生物合成有关的代谢途径以外,很少有制药公司试图研究中断代谢途径的可能性。在本文中,我们描述了细菌蛋白酶在感染过程中的多种新颖作用,作为一个特定的例子,它是来自牙龈卟啉单胞菌(一种牙周病原体)的酶,该酶已知与牙周病的发生和发展有关。以这种方式,我们能够证明开发针对这类酶成员的合成抑制剂作为潜在的第二代抗生素的概念。这样的化合物不仅可以证明在延缓细菌病原体的生长和增殖方面有价值,而且可以导致使用这类抑制剂来抵抗其他感染性生物的入侵。

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