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Genome-Scale Identification of Essential Metabolic Processes for Targeting the Plasmodium Liver Stage.大规模鉴定靶向疟原虫肝期的必需代谢过程。
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Transcriptome analysis of Plasmodium berghei during exo-erythrocytic development.疟原虫在红细胞外发育过程中的转录组分析。
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Antimalarial pantothenamide metabolites target acetyl-coenzyme A biosynthesis in .抗疟泛酰巯基乙胺代谢物靶向.中的乙酰辅酶 A 生物合成。
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Leishmania heme uptake involves LmFLVCRb, a novel porphyrin transporter essential for the parasite.利什曼原虫摄取血红素涉及 LmFLVCRb,一种新型卟啉转运蛋白,对寄生虫至关重要。
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顶复门生物中维生素和辅因子的获取:合成与补救。

Vitamin and cofactor acquisition in apicomplexans: Synthesis salvage.

机构信息

Department of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva CMU, 1 Rue Michel-Servet, 1211 Geneva 4 Switzerland.

Department of Microbiology and Molecular Medicine, Faculty of Medicine, University of Geneva CMU, 1 Rue Michel-Servet, 1211 Geneva 4 Switzerland

出版信息

J Biol Chem. 2020 Jan 17;295(3):701-714. doi: 10.1074/jbc.AW119.008150. Epub 2019 Nov 25.

DOI:10.1074/jbc.AW119.008150
PMID:31767680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6970920/
Abstract

The Apicomplexa phylum comprises diverse parasitic organisms that have evolved from a free-living ancestor. These obligate intracellular parasites exhibit versatile metabolic capabilities reflecting their capacity to survive and grow in different hosts and varying niches. Determined by nutrient availability, they either use their biosynthesis machineries or largely depend on their host for metabolite acquisition. Because vitamins cannot be synthesized by the mammalian host, the enzymes required for their synthesis in apicomplexan parasites represent a large repertoire of potential therapeutic targets. Here, we review recent advances in metabolic reconstruction and functional studies coupled to metabolomics that unravel the interplay between biosynthesis and salvage of vitamins and cofactors in apicomplexans. A particular emphasis is placed on , during both its acute and latent stages of infection.

摘要

顶复门(Apicomplexa)包含了多种从自由生活的祖先进化而来的寄生生物。这些专性细胞内寄生虫表现出多样的代谢能力,反映了它们在不同宿主和不同小生境中生存和生长的能力。根据营养物质的可利用性,它们要么利用自己的生物合成机制,要么在很大程度上依赖宿主获取代谢物。由于哺乳动物宿主不能合成维生素,因此在顶复门寄生虫中,用于合成这些维生素的酶代表了大量潜在的治疗靶点。在这里,我们回顾了代谢重建和功能研究的最新进展,这些研究结合代谢组学揭示了顶复门生物合成和维生素及辅因子回收之间的相互作用。特别强调了疟原虫在急性和潜伏感染阶段的代谢途径。