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      The regulator of G-protein signalling Thn1 links pheromone response to volatile production in Schizophyllum commune : Thn1 controls mating and VOC production

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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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            Biochemistry of plant volatiles.

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              Genome sequence of the model mushroom Schizophyllum commune.

              Much remains to be learned about the biology of mushroom-forming fungi, which are an important source of food, secondary metabolites and industrial enzymes. The wood-degrading fungus Schizophyllum commune is both a genetically tractable model for studying mushroom development and a likely source of enzymes capable of efficient degradation of lignocellulosic biomass. Comparative analyses of its 38.5-megabase genome, which encodes 13,210 predicted genes, reveal the species's unique wood-degrading machinery. One-third of the 471 genes predicted to encode transcription factors are differentially expressed during sexual development of S. commune. Whereas inactivation of one of these, fst4, prevented mushroom formation, inactivation of another, fst3, resulted in more, albeit smaller, mushrooms than in the wild-type fungus. Antisense transcripts may also have a role in the formation of fruiting bodies. Better insight into the mechanisms underlying mushroom formation should affect commercial production of mushrooms and their industrial use for producing enzymes and pharmaceuticals.
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                Author and article information

                Journal
                Environmental Microbiology
                Environ Microbiol
                Wiley
                14622912
                October 2018
                October 2018
                September 17 2018
                : 20
                : 10
                : 3684-3699
                Affiliations
                [1 ]Friedrich Schiller University Jena; Institute of Microbiology, Microbial Communication; Neugasse 25, 07743, Jena Germany
                [2 ]Max Planck Institute for Chemical Ecology; Bioorganic Chemistry, Hans-Knöll-Straße 8, 07745, Jena Germany
                [3 ]Leibnitz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, Molecular and Applied Microbiology; Adolf-Reichwein-Straße 23, 07745, Jena Germany
                Article
                10.1111/1462-2920.14369
                b01cd341-bea0-46b6-ada7-97205fc0ad2e
                © 2018

                http://doi.wiley.com/10.1002/tdm_license_1.1

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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