Chromomycin, an antibiotic produced by Streptomyces flaviscleroticus might play a role in the resistance to oxidative stress and is essential for viability in stationary phase.


Journal

Environmental microbiology
ISSN: 1462-2920
Titre abrégé: Environ Microbiol
Pays: England
ID NLM: 100883692

Informations de publication

Date de publication:
02 2019
Historique:
received: 12 10 2017
revised: 13 12 2018
accepted: 20 12 2018
pubmed: 27 12 2018
medline: 21 4 2020
entrez: 27 12 2018
Statut: ppublish

Résumé

The well-known role of antibiotics in killing sensitive organisms has been challenged by the effects they exert at subinhibitory concentrations. Unfortunately, there are very few published reports on the advantages these molecules may confer to their producers. This study describes the construction of a genetically verified deletion mutant of Streptomyces flaviscleroticus unable to synthesize chromomycin. This mutant was characterized by a rapid loss of viability in stationary phase that was correlated with high oxidative stress and altered antioxidant defences. Altered levels of key metabolites in the mutant signalled a redistribution of the glycolytic flux toward the PPP to generate NADPH to fight oxidative stress as well as reduction of ATP-phosphofructokinase and Krebs cycle enzymes activities. These changes were correlated with a shift in the preference for carbon utilization from glucose to amino acids. Remarkably, chromomycin at subinhibitory concentration increased longevity of the non-producer and restored most of the phenotypic features' characteristic of the wild type strain. Altogether these observations suggest that chromomycin may have antioxidant properties that would explain, at least in part, some of the phenotypes of the mutant. Our observations warrant reconsideration of the secondary metabolite definition and raise the possibility of crucial roles for their producers.

Identifiants

pubmed: 30585380
doi: 10.1111/1462-2920.14515
doi:

Substances chimiques

Anti-Bacterial Agents 0
Chromomycins 0
NADP 53-59-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

814-826

Subventions

Organisme : Indian Council of Medical Research
ID : 80/844/2013/ECD-I
Pays : International

Informations de copyright

© 2018 Society for Applied Microbiology and John Wiley & Sons Ltd.

Auteurs

Divya Prajapati (D)

Department of Bio-Chemistry, The Maharaja Sayajirao University of Baroda, Baroda, 390003, Gujarat, India.

Namita Kumari (N)

Center for Sickle Cell Disease, Howard University, Washington, DC, 20059.

Keyur Dave (K)

Cellcys Labs Pvt. Ltd., Mumbai, 400104, India.

Vaidehi Chatupale (V)

Department of Bio-Chemistry, The Maharaja Sayajirao University of Baroda, Baroda, 390003, Gujarat, India.

Jayashree Pohnerkar (J)

Department of Bio-Chemistry, The Maharaja Sayajirao University of Baroda, Baroda, 390003, Gujarat, India.

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Classifications MeSH