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AllR Controls the Expression of Streptomyces coelicolor Allantoin Pathway Genes.

Authors :
Navone L
Macagno JP
Licona-Cassani C
Marcellin E
Nielsen LK
Gramajo H
Rodriguez E
Source :
Applied and environmental microbiology [Appl Environ Microbiol] 2015 Oct; Vol. 81 (19), pp. 6649-59. Date of Electronic Publication: 2015 Jul 17.
Publication Year :
2015

Abstract

Streptomyces species are native inhabitants of soil, a natural environment where nutrients can be scarce and competition fierce. They have evolved ways to metabolize unusual nutrients, such as purines and its derivatives, which are highly abundant in soil. Catabolism of these uncommon carbon and nitrogen sources needs to be tightly regulated in response to nutrient availability and environmental stimulus. Recently, the allantoin degradation pathway was characterized in Streptomyces coelicolor. However, there are questions that remained unanswered, particularly regarding pathway regulation. Here, using a combination of proteomics and genetic approaches, we identified the negative regulator of the allantoin pathway, AllR. In vitro studies confirmed that AllR binds to the promoter regions of allantoin catabolic genes and determined the AllR DNA binding motif. In addition, effector studies showed that allantoic acid, and glyoxylate, to a lesser extent, inhibit the binding of AllR to the DNA. Inactivation of AllR repressor leads to the constitutive expression of the AllR regulated genes and intriguingly impairs actinorhodin and undecylprodigiosin production. Genetics and proteomics analysis revealed that among all genes from the allantoin pathway that are upregulated in the allR mutant, the hyi gene encoding a hydroxypyruvate isomerase (Hyi) is responsible of the impairment of antibiotic production.<br /> (Copyright © 2015, American Society for Microbiology. All Rights Reserved.)

Details

Language :
English
ISSN :
1098-5336
Volume :
81
Issue :
19
Database :
MEDLINE
Journal :
Applied and environmental microbiology
Publication Type :
Academic Journal
Accession number :
26187964
Full Text :
https://doi.org/10.1128/AEM.02098-15