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质体生物合成途径在顶复门寄生虫中的作用:对药物研发的启示。

The shikimate pathway in apicomplexan parasites: implications for drug development.

机构信息

Institute for Medical Biotechnology, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.

出版信息

Front Biosci (Landmark Ed). 2013 Jun 1;18(3):944-69. doi: 10.2741/4155.

Abstract

The shikimate pathway provides basic building blocks for a variety of aromatic compounds including aromatic amino acids, ubiquinone, folate and compounds of the secondary metabolism. The seven enzymatic reactions of the pathway lead to the generation of chorismate from simple products of the carbohydrate metabolism, namely erythrose 4-phosphate and phosphoenolpyruvate. The shikimate pathway is present in plants, bacteria, fungi and chromalveolata to which the apicomplexan parasites belong. As it is absent from humans, the enzymes of the shikimate pathway are attractive targets for antimicrobial drug development. Inhibition of the pathway is effective in controlling growth of certain apicomplexan parasites including the malaria parasite Plasmodium falciparum. Yet, despite being an attractive drug target, our knowledge of the shikimate pathway in this parasite group is lacking. The current review summarizes the available information and discusses aspects of the genetic organization of the shikimate pathway in apicomplexan parasites. Compounds acting on shikimate pathway enzymes will be presented and discussed in light of their impact for antiapicomplexan/antiplasmodial drug development.

摘要

莽草酸途径为多种芳香族化合物提供了基本构建模块,包括芳香族氨基酸、泛醌、叶酸和次级代谢产物。该途径的 7 个酶促反应导致从碳水化合物代谢的简单产物,即赤藓糖 4-磷酸和磷酸烯醇丙酮酸,生成分支酸。莽草酸途径存在于植物、细菌、真菌和 Chromalveolata 中,锥体虫寄生虫属于 Chromalveolata。由于人类缺乏该途径,因此该途径的酶是开发抗菌药物的有吸引力的靶标。抑制该途径可有效控制某些锥体虫寄生虫的生长,包括疟原虫 Plasmodium falciparum。然而,尽管它是一个有吸引力的药物靶点,但我们对该寄生虫群中莽草酸途径的了解还很缺乏。目前的综述总结了现有的信息,并讨论了锥体虫寄生虫中莽草酸途径的遗传组织的各个方面。将根据它们对抗锥体虫/抗疟药物开发的影响,介绍和讨论作用于莽草酸途径酶的化合物。

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