scispace - formally typeset
Open AccessJournal ArticleDOI

Novel inhibitors of the condensing enzymes of the type II fatty acid synthase of pea (Pisum sativum)

TLDR
The general activity of thiolactomycin and its derivatives against these FAS condensation reactions is demonstrated, and it is suggested that such compounds will be useful for further detailed studies of inhibition and for use as pharmaceuticals against Type II FASs of pathogens.
Abstract
The type II fatty acid synthases (FASs) of higher plants (and Escherichia coli) contain three condensing enzymes called beta-ketoacyl-ACP synthases (KAS), where ACP is acyl-carrier-protein. We have used novel derivatives of the antibiotic thiolactomycin to inhibit these enzymes. Overall de novo fatty acid biosynthesis was measured using [1-(14)C]acetate substrate and chloroplast preparations from pea leaves, and [1-(14)C]laurate was used to distinguish between the effects of the inhibitors on KAS I from those on KAS II. In addition, the activities of these enzymes, together with the short-chain condensing enzyme, KAS III, were measured directly. Six analogues were tested and two, both with extended hydrocarbon side chains, were found to be more effective inhibitors than thiolactomycin. Incubations with chloroplasts and direct assay of the individual condensing enzymes showed that all three compounds inhibited the pea FAS condensing enzymes in the order KAS II > KAS I > KAS III. These results demonstrate the general activity of thiolactomycin and its derivatives against these FAS condensation reactions, and suggest that such compounds will be useful for further detailed studies of inhibition and for use as pharmaceuticals against Type II FASs of pathogens.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Bacterial Fatty Acid Biosynthesis: Targets for Antibacterial Drug Discovery

TL;DR: This review encompasses the known inhibitors and prospective targets for new antibacterial compounds found in microbial fatty acid biosynthesis and their potential as lead compounds in the development of new antibacterials.
Journal ArticleDOI

Lipid biosynthesis as a target for antibacterial agents.

TL;DR: The site of action of isoniazid, used in the treatment of tuberculosis for 50 years, and the consumer antimicrobial agent triclosan were revealed recently to be the enoyl-ACP reductase of the type II FAS, which contrasts sharply with the type I FAS of eukaryotes.
Journal ArticleDOI

Inhibition of beta-ketoacyl-acyl carrier protein synthases by thiolactomycin and cerulenin. Structure and mechanism.

TL;DR: FabB[H333N] was significantly more resistant to both antibiotics than FabB and had an affinity for TLM an order of magnitude less than the wild-type enzyme, illustrating that the two-histidine active site architecture is critical to protein-antibiotic interaction.
Journal ArticleDOI

A Type II Pathway for Fatty Acid Biosynthesis Presents Drug Targets in Plasmodium falciparum

TL;DR: This study substantiates the importance of fatty acid synthesis for blood-stage parasite survival and shows that this pathway provides scope for the development of novel antimalarial drugs.
Journal ArticleDOI

Inhibitors of fatty acid synthesis as antimicrobial chemotherapeutics

TL;DR: Three compounds target the FabI enoyl-ACP reductase step; isoniazid, a clinically used antituberculosis drug, triclosan, a widely used consumer antimicrobial, and diazaborines, and the mechanisms of action of these compounds, as well as the potential development of new drugs targeted against this pathway are discussed.
References
More filters
Journal ArticleDOI

Copper enzymes in isolated chloroplasts. polyphenoloxidase in beta vulgaris

TL;DR: Evidence that a copper enzyme, polyphenoloxidase (otherwise known as tyrosinase or catecholase), is localized in the chloroplasts of spinach beet (chard), Beta vu?garis is presented.
Journal ArticleDOI

Nuclear-encoded proteins target to the plastid in Toxoplasma gondii and Plasmodium falciparum

TL;DR: In this paper, nuclear genes encoding ribosomal proteins S9 and L28 and the fatty acid biosynthetic enzymes acyl carrier protein (ACP), β-ketoacyl-ACP synthase III (FabH), and β-hydroxyacyl -ACP dehydratase (FabZ) were identified.
Journal ArticleDOI

The rapid incorporation of phosphate into mitochondrial lipids.

TL;DR: Studies on the early labeling of lipid in mitochondria by P32-labeled inorganic phosphate indicate that it is not an intermediate in oxidative phosphorylation.
Journal ArticleDOI

Structure of the complex between the antibiotic cerulenin and its target, beta-ketoacyl-acyl carrier protein synthase.

TL;DR: The crystal structure of the complex of the enzyme from Escherichia coli, and the fungal mycotoxin cerulenin reveals that the inhibitor is bound in a hydrophobic pocket formed at the dimer interface and there is thus room for improvement through structure based design.
Related Papers (5)