» Articles » PMID: 32069930

A Challenging View: Antibiotics Play a Role in the Regulation of the Energetic Metabolism of the Producing Bacteria

Overview
Specialty Pharmacology
Date 2020 Feb 20
PMID 32069930
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Antibiotics are often considered as weapons conferring a competitive advantage to their producers in their ecological niche. However, since these molecules are produced in specific environmental conditions, notably phosphate limitation that triggers a specific metabolic state, they are likely to play important roles in the physiology of the producing bacteria that have been overlooked. Our recent experimental data as well as careful analysis of the scientific literature led us to propose that, in conditions of moderate to severe phosphate limitation-conditions known to generate energetic stress-antibiotics play crucial roles in the regulation of the energetic metabolism of the producing bacteria. A novel classification of antibiotics into types I, II, and III, based on the nature of the targets of these molecules and on their impact on the cellular physiology, is proposed. Type I antibiotics are known to target cellular membranes, inducing energy spilling and cell lysis of a fraction of the population to provide nutrients, and especially phosphate, to the surviving population. Type II antibiotics inhibit respiration through different strategies, to reduce ATP generation in conditions of low phosphate availability. Lastly, Type III antibiotics that are known to inhibit ATP consuming anabolic processes contribute to ATP saving in conditions of phosphate starvation.

Citing Articles

Optimizing broiler growth, health, and meat quality with citric acid- assessing the optimal dose and environmental impact: Citric acid in Broiler Health and Production.

Sharifuzzaman M, Mun H, Ampode K, Lagua E, Park H, Kim Y Poult Sci. 2024; 104(2):104668.

PMID: 39705837 PMC: 11728898. DOI: 10.1016/j.psj.2024.104668.


Expression of Multiple Copies of the Lon Protease Gene Resulted in Increased Antibiotic Production, Osmotic and UV Stress Resistance in Streptomyces coelicolor A3(2).

Yilmaz H, Yaradir E, Tunca S Curr Microbiol. 2024; 82(1):43.

PMID: 39690306 DOI: 10.1007/s00284-024-04021-z.


Impact of the Deletion of Genes of the Nitrogen Metabolism on Triacylglycerol, Cardiolipin and Actinorhodin Biosynthesis in .

Abreu S, Lejeune C, David M, Chaminade P, Virolle M Microorganisms. 2024; 12(8).

PMID: 39203402 PMC: 11356632. DOI: 10.3390/microorganisms12081560.


Functional connexion of bacterioferritin in antibiotic production and morphological differentiation in Streptomyces coelicolor.

Garcia-Martin J, Garcia-Abad L, Santamaria R, Diaz M Microb Cell Fact. 2024; 23(1):234.

PMID: 39182107 PMC: 11344345. DOI: 10.1186/s12934-024-02510-1.


Consequences of the deletion of the major specialized metabolite biosynthetic pathways of Streptomyces coelicolor on the metabolome and lipidome of this strain.

Lejeune C, Abreu S, Guerard F, Askora A, David M, Chaminade P Microb Biotechnol. 2024; 17(8):e14538.

PMID: 39093579 PMC: 11296114. DOI: 10.1111/1751-7915.14538.


References
1.
Malpartida F, Hopwood D . Molecular cloning of the whole biosynthetic pathway of a Streptomyces antibiotic and its expression in a heterologous host. Nature. 1984; 309(5967):462-4. DOI: 10.1038/309462a0. View

2.
Stubbendieck R, Straight P . Multifaceted Interfaces of Bacterial Competition. J Bacteriol. 2016; 198(16):2145-55. PMC: 4966439. DOI: 10.1128/JB.00275-16. View

3.
Tsao S, Rudd B, He X, Chang C, Floss H . Identification of a red pigment from Streptomyces coelicolor A3(2) as a mixture of prodigiosin derivatives. J Antibiot (Tokyo). 1985; 38(1):128-31. DOI: 10.7164/antibiotics.38.128. View

4.
Hopwood D . How do antibiotic-producing bacteria ensure their self-resistance before antibiotic biosynthesis incapacitates them?. Mol Microbiol. 2007; 63(4):937-40. DOI: 10.1111/j.1365-2958.2006.05584.x. View

5.
Bakal C, Davies J . No longer an exclusive club: eukaryotic signalling domains in bacteria. Trends Cell Biol. 1999; 10(1):32-8. DOI: 10.1016/s0962-8924(99)01681-5. View