» Articles » PMID: 15043389

Isoprenoid Biosynthesis As a Novel Target for Antibacterial and Antiparasitic Drugs

Overview
Date 2004 Mar 27
PMID 15043389
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

The mevalonate-independent methylerythritol phosphate pathway is a long overlooked metabolic pathway for isoprenoid biosynthesis. It is present in most bacteria, including pathogens and opportunistic pathogens, in some unicellular eukaryotes, including the parasite responsible for malaria, and in the chloroplasts of all phototrophic organisms. It represents an alternative to the mevalonate pathway, which is only present in animals, fungi, the plant cytoplasm, archaebacteria and some eubacteria. This biosynthetic pathway is thus a potential target for antibacterial and antiparasitic drugs. An isopentenyl diphosphate isomerase that differs from the previously known isopentenyl diphosphate isomerase found in all other organisms, including animals, was discovered in several Gram-positive bacteria possessing the mevalonate pathway, adding another target related to isoprenoid biosynthesis.

Citing Articles

New Application of Saligenyl Prodrugs Approach for the Delivery of Fosfoxacin Derivatives in Mycobacteria.

Munier M, Tritsch D, Lievremont D, Rohmer M, Grosdemange-Billiard C Molecules. 2023; 28(23).

PMID: 38067444 PMC: 10707747. DOI: 10.3390/molecules28237713.


Microbial ()-4-hydroxy-3-methylbut-2-enyl pyrophosphate reductase (IspH) and its biotechnological potential: A mini review.

Huang S, Xue Y, Ma Y, Zhou C Front Bioeng Biotechnol. 2022; 10:1057938.

PMID: 36524053 PMC: 9745026. DOI: 10.3389/fbioe.2022.1057938.


The Reductive Dehydroxylation Catalyzed by IspH, a Source of Inspiration for the Development of Novel Anti-Infectives.

Jobelius H, Bianchino G, Borel F, Chaignon P, Seemann M Molecules. 2022; 27(3).

PMID: 35163971 PMC: 8837944. DOI: 10.3390/molecules27030708.


YdfD, a Lysis Protein of the Qin Prophage, Is a Specific Inhibitor of the IspG-Catalyzed Step in the MEP Pathway of .

Lu Z, Wang B, Qiu Z, Zhang R, Zheng J, Jia Z Int J Mol Sci. 2022; 23(3).

PMID: 35163484 PMC: 8835842. DOI: 10.3390/ijms23031560.


α,α-Difluorophosphonohydroxamic Acid Derivatives among the Best Antibacterial Fosmidomycin Analogues.

Dreneau A, Krebs F, Munier M, Ngov C, Tritsch D, Lievremont D Molecules. 2021; 26(16).

PMID: 34443699 PMC: 8397956. DOI: 10.3390/molecules26165111.