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      Secondary Metabolites Produced during the Germination of Streptomyces coelicolor

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          Abstract

          Spore awakening is a series of actions that starts with purely physical processes and continues via the launching of gene expression and metabolic activities, eventually achieving a vegetative phase of growth. In spore-forming microorganisms, the germination process is controlled by intra- and inter-species communication. However, in the Streptomyces clade, which is capable of developing a plethora of valuable compounds, the chemical signals produced during germination have not been systematically studied before. Our previously published data revealed that several secondary metabolite biosynthetic genes are expressed during germination. Therefore, we focus here on the secondary metabolite production during this developmental stage. Using high-performance liquid chromatography-mass spectrometry, we found that the sesquiterpenoid antibiotic albaflavenone, the polyketide germicidin A, and chalcone are produced during germination of the model streptomycete, S. coelicolor. Interestingly, the last two compounds revealed an inhibitory effect on the germination process. The secondary metabolites originating from the early stage of microbial growth may coordinate the development of the producer ( quorum sensing) and/or play a role in competitive microflora repression ( quorum quenching) in their nature environments.

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          Most cited references73

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          Quorum sensing: cell-to-cell communication in bacteria.

          Bacteria communicate with one another using chemical signal molecules. As in higher organisms, the information supplied by these molecules is critical for synchronizing the activities of large groups of cells. In bacteria, chemical communication involves producing, releasing, detecting, and responding to small hormone-like molecules termed autoinducers . This process, termed quorum sensing, allows bacteria to monitor the environment for other bacteria and to alter behavior on a population-wide scale in response to changes in the number and/or species present in a community. Most quorum-sensing-controlled processes are unproductive when undertaken by an individual bacterium acting alone but become beneficial when carried out simultaneously by a large number of cells. Thus, quorum sensing confuses the distinction between prokaryotes and eukaryotes because it enables bacteria to act as multicellular organisms. This review focuses on the architectures of bacterial chemical communication networks; how chemical information is integrated, processed, and transduced to control gene expression; how intra- and interspecies cell-cell communication is accomplished; and the intriguing possibility of prokaryote-eukaryote cross-communication.
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            Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2).

            Streptomyces coelicolor is a representative of the group of soil-dwelling, filamentous bacteria responsible for producing most natural antibiotics used in human and veterinary medicine. Here we report the 8,667,507 base pair linear chromosome of this organism, containing the largest number of genes so far discovered in a bacterium. The 7,825 predicted genes include more than 20 clusters coding for known or predicted secondary metabolites. The genome contains an unprecedented proportion of regulatory genes, predominantly those likely to be involved in responses to external stimuli and stresses, and many duplicated gene sets that may represent 'tissue-specific' isoforms operating in different phases of colonial development, a unique situation for a bacterium. An ancient synteny was revealed between the central 'core' of the chromosome and the whole chromosome of pathogens Mycobacterium tuberculosis and Corynebacterium diphtheriae. The genome sequence will greatly increase our understanding of microbial life in the soil as well as aiding the generation of new drug candidates by genetic engineering.
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              Bacterial quorum sensing: its role in virulence and possibilities for its control.

              Quorum sensing is a process of cell-cell communication that allows bacteria to share information about cell density and adjust gene expression accordingly. This process enables bacteria to express energetically expensive processes as a collective only when the impact of those processes on the environment or on a host will be maximized. Among the many traits controlled by quorum sensing is the expression of virulence factors by pathogenic bacteria. Here we review the quorum-sensing circuits of Staphylococcus aureus, Bacillus cereus, Pseudomonas aeruginosa, and Vibrio cholerae. We outline these canonical quorum-sensing mechanisms and how each uniquely controls virulence factor production. Additionally, we examine recent efforts to inhibit quorum sensing in these pathogens with the goal of designing novel antimicrobial therapeutics.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                13 December 2017
                2017
                : 8
                : 2495
                Affiliations
                [1] 1First Faculty of Medicine, Institute of Immunology and Microbiology, Charles University , Prague, Czechia
                [2] 2Institute of Microbiology, The Czech Academy of Sciences , Prague, Czechia
                [3] 3Chemistry Department, Faculty of Science, J. E. Purkinje University , Ústí nad Labem, Czechia
                Author notes

                Edited by: Dirk Tischler, Freiberg University of Mining and Technology, Germany

                Reviewed by: Dennis Claessen, Leiden University, Netherlands; Yinhua Lu, Shanghai Institutes for Biological Sciences (CAS), China

                *Correspondence: Jan Bobek jan.bobek@ 123456lf1.cuni.cz

                This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2017.02495
                5733532
                29326665
                729a6055-9833-4f72-aa35-a03aae52e3cd
                Copyright © 2017 Čihák, Kameník, Šmídová, Bergman, Benada, Kofroňová, Petříčková and Bobek.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 29 August 2017
                : 30 November 2017
                Page count
                Figures: 6, Tables: 3, Equations: 0, References: 80, Pages: 13, Words: 9969
                Funding
                Funded by: Univerzita Karlova v Praze 10.13039/100007397
                Award ID: Progres Q26/LF1
                Award ID: SVV260369
                Funded by: Grantová Agentura, Univerzita Karlova 10.13039/100007543
                Award ID: 160214
                Funded by: Univerzite Jan Evangelista Purkyne v Ústí nad Labem 10.13039/501100004011
                Award ID: UJEP-SGS-173-07-01
                Funded by: Czech research infrastructure for systems biology C4SYS
                Award ID: LM2015055
                Funded by: Ministerstvo Školství, Mládeže a Telovýchovy 10.13039/501100001823
                Award ID: LO1509
                Funded by: EU - Horizon 2020 10.13039/501100007601
                Award ID: Operational Program Prague–Competitiveness project (CZ.2.16/3.1.00/24023)
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                spore germination,streptomyces,cell signaling,secondary metabolism,albaflavenone,germicidin,chalcone

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