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      Mechanism and regulation of sorbicillin biosynthesis by Penicillium chrysogenum

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          Summary

          Penicillium chrysogenum is a filamentous fungus that is used to produce β‐lactams at an industrial scale. At an early stage of classical strain improvement, the ability to produce the yellow‐coloured sorbicillinoids was lost through mutation. Sorbicillinoids are highly bioactive of great pharmaceutical interest. By repair of a critical mutation in one of the two polyketide synthases in an industrial P. chrysogenum strain, sorbicillinoid production was restored at high levels. Using this strain, the sorbicillin biosynthesis pathway was elucidated through gene deletion, overexpression and metabolite profiling. The polyketide synthase enzymes SorA and SorB are required to generate the key intermediates sorbicillin and dihydrosorbicillin, which are subsequently converted to (dihydro)sorbillinol by the FAD‐dependent monooxygenase SorC and into the final product oxosorbicillinol by the oxidoreductase SorD. Deletion of either of the two pks genes not only impacted the overall production but also strongly reduce the expression of the pathway genes. Expression is regulated through the interplay of two transcriptional regulators: SorR1 and SorR2. SorR1 acts as a transcriptional activator, while SorR2 controls the expression of sorR1. Furthermore, the sorbicillinoid pathway is regulated through a novel autoinduction mechanism where sorbicillinoids activate transcription.

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          Most cited references31

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          Regulation of fungal secondary metabolism.

          Fungi produce a multitude of low-molecular-mass compounds known as secondary metabolites, which have roles in a range of cellular processes such as transcription, development and intercellular communication. In addition, many of these compounds now have important applications, for instance, as antibiotics or immunosuppressants. Genome mining efforts indicate that the capability of fungi to produce secondary metabolites has been substantially underestimated because many of the fungal secondary metabolite biosynthesis gene clusters are silent under standard cultivation conditions. In this Review, I describe our current understanding of the regulatory elements that modulate the transcription of genes involved in secondary metabolism. I also discuss how an improved knowledge of these regulatory elements will ultimately lead to a better understanding of the physiological and ecological functions of these important compounds and will pave the way for a novel avenue to drug discovery through targeted activation of silent gene clusters.
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            Regulation of secondary metabolism in filamentous fungi.

            Fungal secondary metabolites are of intense interest to humankind due to their pharmaceutical (antibiotics) and/or toxic (mycotoxins) properties. In the past decade, tremendous progress has been made in understanding the genes that are associated with production of various fungal secondary metabolites. Moreover, the regulatory mechanisms controlling biosynthesis of diverse groups of secondary metabolites have been unveiled. In this review, we present the current understanding of the genetic regulation of secondary metabolism from clustering of biosynthetic genes to global regulators balancing growth, sporulation, and secondary metabolite production in selected fungi with emphasis on regulation of metabolites of agricultural concern. Particularly, the roles of G protein signaling components and developmental regulators in the mycotoxin sterigmatocystin biosynthesis in the model fungus Aspergillus nidulans are discussed in depth.
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              CRISPR/Cas9 Based Genome Editing of Penicillium chrysogenum.

              CRISPR/Cas9 based systems have emerged as versatile platforms for precision genome editing in a wide range of organisms. Here we have developed powerful CRISPR/Cas9 tools for marker-based and marker-free genome modifications in Penicillium chrysogenum, a model filamentous fungus and industrially relevant cell factory. The developed CRISPR/Cas9 toolbox is highly flexible and allows editing of new targets with minimal cloning efforts. The Cas9 protein and the sgRNA can be either delivered during transformation, as preassembled CRISPR-Cas9 ribonucleoproteins (RNPs) or expressed from an AMA1 based plasmid within the cell. The direct delivery of the Cas9 protein with in vitro synthesized sgRNA to the cells allows for a transient method for genome engineering that may rapidly be applicable for other filamentous fungi. The expression of Cas9 from an AMA1 based vector was shown to be highly efficient for marker-free gene deletions.
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                Author and article information

                Contributors
                a.j.m.driessen@rug.nl
                Journal
                Microb Biotechnol
                Microb Biotechnol
                10.1111/(ISSN)1751-7915
                MBT2
                Microbial Biotechnology
                John Wiley and Sons Inc. (Hoboken )
                1751-7915
                15 June 2017
                July 2017
                : 10
                : 4 , Thematic Issue on Biofilms: Microbial Works of Art ( doiID: 10.1111/mbt2.2017.10.issue-4 )
                : 958-968
                Affiliations
                [ 1 ] Molecular MicrobiologyGroningen Biomolecular Sciences and Biotechnology Institute University of Groningen Nijenborgh 7, 9747 AG GroningenThe Netherlands
                [ 2 ] Synthetic Biology and Cell Engineering Groningen Biomolecular Sciences and Biotechnology InstituteUniversity of Groningen Nijenborgh 7, 9747 AG GroningenThe Netherlands
                [ 3 ]DSM Biotechnology Center Alexander Fleminglaan 1 2613 AX DelftThe Netherlands
                [ 4 ]Present address: Biology and Biological Engineering Industrial BiotechnologyChalmers University of Technology Kemigarden 4 GöteborgSweden
                Author notes
                [*] [* ]For correspondence. E‐mail a.j.m.driessen@ 123456rug.nl ; Tel. +31 50 363 2150; Fax +31 50 363 2150.
                Article
                MBT212736
                10.1111/1751-7915.12736
                5481523
                28618182
                98920454-3ff6-4bd5-9c80-e4fd288893c3
                © 2017 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 March 2017
                : 25 April 2017
                : 28 April 2017
                Page count
                Figures: 4, Tables: 0, Pages: 11, Words: 6364
                Funding
                Funded by: Consejo Nacional de Ciencia y Tecnología (CONACyT, México)
                Funded by: Becas Complemento SEP (México)
                Funded by: European Union's Seventh Framework Programme
                Award ID: FP7/207‐2013
                Funded by: NWO|Stichting voor de Technische Wetenschappen
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                mbt212736
                July 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.1 mode:remove_FC converted:23.06.2017

                Biotechnology
                Biotechnology

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