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Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress

Streptomyces are aerobic Gram-positive bacteria characterized by a complex life cycle that includes hyphae differentiation and spore formation. Morphological differentiation is triggered by stressful conditions and takes place in a pro-oxidant environment, which sets the basis for an involvement of...

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Autores principales: Beites, Tiago, Oliveira, Paulo, Rioseras, Beatriz, Pires, Sílvia D. S., Oliveira, Rute, Tamagnini, Paula, Moradas-Ferreira, Pedro, Manteca, Ángel, Mendes, Marta V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530454/
https://www.ncbi.nlm.nih.gov/pubmed/26256439
http://dx.doi.org/10.1038/srep12887
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author Beites, Tiago
Oliveira, Paulo
Rioseras, Beatriz
Pires, Sílvia D. S.
Oliveira, Rute
Tamagnini, Paula
Moradas-Ferreira, Pedro
Manteca, Ángel
Mendes, Marta V.
author_facet Beites, Tiago
Oliveira, Paulo
Rioseras, Beatriz
Pires, Sílvia D. S.
Oliveira, Rute
Tamagnini, Paula
Moradas-Ferreira, Pedro
Manteca, Ángel
Mendes, Marta V.
author_sort Beites, Tiago
collection PubMed
description Streptomyces are aerobic Gram-positive bacteria characterized by a complex life cycle that includes hyphae differentiation and spore formation. Morphological differentiation is triggered by stressful conditions and takes place in a pro-oxidant environment, which sets the basis for an involvement of the oxidative stress response in this cellular process. Characterization of the phenotypic traits of Streptomyces natalensis ΔkatA1 (mono-functional catalase) and ΔcatR (Fur-like repressor of katA1 expression) strains in solid medium revealed that both mutants had an impaired morphological development process. The sub-lethal oxidative stress caused by the absence of KatA1 resulted in the formation of a highly proliferative and undifferentiated vegetative mycelium, whereas de-repression of CatR regulon, from which KatA1 is the only known representative, resulted in the formation of scarce aerial mycelium. Both mutant strains had the transcription of genes associated with aerial mycelium formation and biosynthesis of the hyphae hydrophobic layer down-regulated. The first round of the programmed cell death (PCD) was inhibited in both strains which caused the prevalence of the transient primary mycelium (MI) over secondary mycelium (MII). Our data shows that the first round of PCD and morphological differentiation in S. natalensis is dependent on oxidative stress in the right amount at the right time.
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spelling pubmed-45304542015-08-11 Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress Beites, Tiago Oliveira, Paulo Rioseras, Beatriz Pires, Sílvia D. S. Oliveira, Rute Tamagnini, Paula Moradas-Ferreira, Pedro Manteca, Ángel Mendes, Marta V. Sci Rep Article Streptomyces are aerobic Gram-positive bacteria characterized by a complex life cycle that includes hyphae differentiation and spore formation. Morphological differentiation is triggered by stressful conditions and takes place in a pro-oxidant environment, which sets the basis for an involvement of the oxidative stress response in this cellular process. Characterization of the phenotypic traits of Streptomyces natalensis ΔkatA1 (mono-functional catalase) and ΔcatR (Fur-like repressor of katA1 expression) strains in solid medium revealed that both mutants had an impaired morphological development process. The sub-lethal oxidative stress caused by the absence of KatA1 resulted in the formation of a highly proliferative and undifferentiated vegetative mycelium, whereas de-repression of CatR regulon, from which KatA1 is the only known representative, resulted in the formation of scarce aerial mycelium. Both mutant strains had the transcription of genes associated with aerial mycelium formation and biosynthesis of the hyphae hydrophobic layer down-regulated. The first round of the programmed cell death (PCD) was inhibited in both strains which caused the prevalence of the transient primary mycelium (MI) over secondary mycelium (MII). Our data shows that the first round of PCD and morphological differentiation in S. natalensis is dependent on oxidative stress in the right amount at the right time. Nature Publishing Group 2015-08-10 /pmc/articles/PMC4530454/ /pubmed/26256439 http://dx.doi.org/10.1038/srep12887 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Beites, Tiago
Oliveira, Paulo
Rioseras, Beatriz
Pires, Sílvia D. S.
Oliveira, Rute
Tamagnini, Paula
Moradas-Ferreira, Pedro
Manteca, Ángel
Mendes, Marta V.
Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress
title Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress
title_full Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress
title_fullStr Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress
title_full_unstemmed Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress
title_short Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress
title_sort streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530454/
https://www.ncbi.nlm.nih.gov/pubmed/26256439
http://dx.doi.org/10.1038/srep12887
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