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      The identification and deletion of the polyketide synthase‐nonribosomal peptide synthase gene responsible for the production of the phytotoxic triticone A/B in the wheat fungal pathogen Pyrenophora tritici‐repentis

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          Summary

          The economically important necrotrophic fungal pathogen, Pyrenophora tritici‐repentis (Ptr), causes tan spot of wheat, a disease typified by foliar necrosis and chlorosis. The culture filtrate of an Australian Ptr isolate, M4, possesses phytotoxic activity and plant bioassay guided discovery led to the purification of necrosis inducing toxins called triticone A and B. High‐resolution LC–MS/MS analysis of the culture filtrate identified an additional 37 triticone‐like compounds. The biosynthetic gene cluster responsible for triticone production (the Ttc cluster) was identified and deletion of TtcA, a hybrid polyketide synthase (PKS)‐nonribosomal peptide synthase (NRPS), abolished production of all triticones. The pathogenicity of mutant ( ttcA) strains was not visibly affected in our assays. We hypothesize that triticones possess general antimicrobial activity important for competition in multi‐microbial environments.

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          Fungal secondary metabolism - from biochemistry to genomics.

          Much of natural product chemistry concerns a group of compounds known as secondary metabolites. These low-molecular-weight metabolites often have potent physiological activities. Digitalis, morphine and quinine are plant secondary metabolites, whereas penicillin, cephalosporin, ergotrate and the statins are equally well known fungal secondary metabolites. Although chemically diverse, all secondary metabolites are produced by a few common biosynthetic pathways, often in conjunction with morphological development. Recent advances in molecular biology, bioinformatics and comparative genomics have revealed that the genes encoding specific fungal secondary metabolites are clustered and often located near telomeres. In this review, we address some important questions, including which evolutionary pressures led to gene clustering, why closely related species produce different profiles of secondary metabolites, and whether fungal genomics will accelerate the discovery of new pharmacologically active natural products.
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            Regulation and Role of Fungal Secondary Metabolites.

            Fungi have the capability to produce a tremendous number of so-called secondary metabolites, which possess a multitude of functions, e.g., communication signals during coexistence with other microorganisms, virulence factors during pathogenic interactions with plants and animals, and in medical applications. Therefore, research on this topic has intensified significantly during the past 10 years and thus knowledge of regulatory mechanisms and the understanding of the role of secondary metabolites have drastically increased. This review aims to depict the complexity of all the regulatory elements involved in controlling the expression of secondary metabolite gene clusters, ranging from epigenetic control and signal transduction pathways to global and specific transcriptional regulators. Furthermore, we give a short overview on the role of secondary metabolites, focusing on the interaction with other microorganisms in the environment as well as on pathogenic relationships.
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              Relationship between secondary metabolism and fungal development.

              Filamentous fungi are unique organisms-rivaled only by actinomycetes and plants-in producing a wide range of natural products called secondary metabolites. These compounds are very diverse in structure and perform functions that are not always known. However, most secondary metabolites are produced after the fungus has completed its initial growth phase and is beginning a stage of development represented by the formation of spores. In this review, we describe secondary metabolites produced by fungi that act as sporogenic factors to influence fungal development, are required for spore viability, or are produced at a time in the life cycle that coincides with development. We describe environmental and genetic factors that can influence the production of secondary metabolites. In the case of the filamentous fungus Aspergillus nidulans, we review the only described work that genetically links the sporulation of this fungus to the production of the mycotoxin sterigmatocystin through a shared G-protein signaling pathway.
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                Author and article information

                Contributors
                yitheng.chooi@uwa.edu.au
                richard.oliver@curtin.edu.au
                Journal
                Environ Microbiol
                Environ. Microbiol
                10.1111/(ISSN)1462-2920
                EMI
                Environmental Microbiology
                John Wiley & Sons, Inc. (Hoboken, USA )
                1462-2912
                1462-2920
                21 November 2019
                December 2019
                : 21
                : 12 , Special Issue on Pathogen and Antimicrobial Resistance Ecology ( doiID: 10.1111/emi.v21.12 )
                : 4875-4886
                Affiliations
                [ 1 ] Centre for Crop and Disease Management Curtin University Perth 6150 Western Australia Australia
                [ 2 ] School of Molecular Sciences The University of Western Australia Perth 6009 Western Australia Australia
                Author notes
                [*] [* ]For correspondence. E‐mail richard.oliver@ 123456curtin.edu.au . yitheng.chooi@ 123456uwa.edu.au . Tel. 08 9266 4818.
                Author information
                https://orcid.org/0000-0002-3502-7612
                https://orcid.org/0000-0001-7719-7524
                https://orcid.org/0000-0001-7290-4154
                Article
                EMI14854
                10.1111/1462-2920.14854
                6915911
                31698543
                b38372b2-16a7-4648-aebf-12b99b0e7c9b
                © 2019 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 09 October 2019
                : 04 November 2019
                : 05 November 2019
                Page count
                Figures: 5, Tables: 0, Pages: 12, Words: 8004
                Funding
                Funded by: Australian Research Council , open-funder-registry 10.13039/501100000923;
                Award ID: Future Fellowship FT160100233
                Award ID: FT160100233
                Funded by: Grains Research and Development Corporation , open-funder-registry 10.13039/501100000980;
                Award ID: CUR00023
                Funded by: Edith Cowan University , open-funder-registry 10.13039/501100001798;
                Funded by: University of Western Australia , open-funder-registry 10.13039/501100001801;
                Funded by: Department of Agriculture , open-funder-registry 10.13039/501100003526;
                Award ID: DW7
                Award ID: DW5
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                December 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.3 mode:remove_FC converted:17.12.2019

                Microbiology & Virology
                Microbiology & Virology

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