Distribution and evolution of nonribosomal peptide synthetase gene clusters in the Ceratocystidaceae

dc.contributor.authorSayari, Mohammad
dc.contributor.authorVan der Nest, Magrieta Aletta
dc.contributor.authorSteenkamp, Emma Theodora
dc.contributor.authorSoal, Nicole Christine
dc.contributor.authorWilken, Pieter Markus
dc.contributor.authorWingfield, Brenda D.
dc.contributor.emailbrenda.wingfield@fabi.up.ac.zaen_ZA
dc.date.accessioned2020-08-24T07:27:26Z
dc.date.available2020-08-24T07:27:26Z
dc.date.issued2019-04-30
dc.descriptionSupplementary file S1. Genome sequence information for the 16 Sordariomycetes representative included in this study. Secondary metabolite unique regions finder (SMURF; www.jcvi.org/smurf/; (22) was used to predict NRPS genes from the Sordariomycetes genomes available from the Joint Genome Institute (JGI; https://jgi.doe.gov/ our-science/science-programs/fungal-genomics/) and the National Centre for Biotechnology Information (NCBI; http://blast.ncbi.nlm.nih.gov/).en_ZA
dc.descriptionSupplementary file S2. To confirm the order of genes within the di erent NRPS clusters identified, a PCR-based approach was used. For each cluster type, primers were designed that allow amplification of individual genes, as well as the regions between them. Correlation between predicted and observed fragment sizes were used as evidence that the specific cluster was correctly assembled.en_ZA
dc.descriptionSupplementary file S3. Blast hits for putative Ceratocystidaceae NRPS biosynthetic cluster genes. For confirmation of the antiSMASH results, we utilized secondary metabolite unique regions finder (SMURF; www.jcvi.org/smurf/; (22). For this purpose, genes that were 15 Kb upstream and downstream of the identified NRPS genes were retrieved and submitted to the BLASTp server at the National Center for Biotechnology Information (NCBI, ftp://ftp.ncbi.nih.gov/blast/) for identification.en_ZA
dc.descriptionSupplementary file S4. The tables below show the predicted nonribosomal peptide synthetase (NRPS) gene clusters predicted by SMURF (secondary metabolite unique regions finder) (22; 37).en_ZA
dc.descriptionSupplementary file S5. Top 10 BLASTp hits for each NRPS sequence. BLASTp search was done against the non-redundant protein sequences in the National Centre for Biotechnology Information database (NCBI; http://blast.ncbi.nlm.nih.gov/), and the top 10 hits are indicated with species where they are found, E-value, percent sequence identity, and coverage. Supplementary file S6. Mapping of RNA reads to di erent genes of the NRPS gene clusters of C. fimbriata, H. moniliformis, and H. omanensis. This included the genes of the monomodular NRPS gene clusters: A, hypothetical protein; B, nonribosomal peptide synthetase; C, siderophore transporter; D, siderophore biosynthesis; E, oxidoreductase; F, ABC transporter; and G, transporter. It also included mapping of RNA reads to di erent genes of multimodular NRPS gene clusters of C. fimbriata, H. moniliformis, and H. omanensis. A, nonribosomal peptide synthetase; B, orntithine monooxygenase; C, endothiapepsin; D, RNA polymerase transcription subunit; and E, aldehyde dehydrogenase. Reads in green and red represent forward and reverse orientation, respectively.en_ZA
dc.descriptionSupplementary file S5. Top 10 BLASTp hits for each NRPS sequence. BLASTp search was done against the non-redundant protein sequences in the National Centre for Biotechnology Information database (NCBI; http://blast.ncbi.nlm.nih.gov/), and the top 10 hits are indicated with species where they are found, E-value, percent sequence identity, and coverage.en_ZA
dc.descriptionSupplementary file S6. Mapping of RNA reads to di erent genes of the NRPS gene clusters of C. fimbriata, H. moniliformis, and H. omanensis. This included the genes of the monomodular NRPS gene clusters: A, hypothetical protein; B, nonribosomal peptide synthetase; C, siderophore transporter; D, siderophore biosynthesis; E, oxidoreductase; F, ABC transporter; and G, transporter. It also included mapping of RNA reads to di erent genes of multimodular NRPS gene clusters of C. fimbriata, H. moniliformis, and H. omanensis. A, nonribosomal peptide synthetase; B, orntithine monooxygenase; C, endothiapepsin; D, RNA polymerase transcription subunit; and E, aldehyde dehydrogenase. Reads in green and red represent forward and reverse orientation, respectively.en_ZA
dc.description.abstractIn filamentous fungi, genes in secondary metabolite biosynthetic pathways are generally clustered. In the case of those pathways involved in nonribosomal peptide production, a nonribosomal peptide synthetase (NRPS) gene is commonly found as a main element of the cluster. Large multifunctional enzymes are encoded by members of this gene family that produce a broad spectrum of bioactive compounds. In this research, we applied genome-based identification of nonribosomal peptide biosynthetic gene clusters in the family Ceratocystidaceae. For this purpose, we used the whole genome sequences of species from the genera Ceratocystis, Davidsoniella, Thielaviopsis, Endoconidiophora, Bretziella, Huntiella, and Ambrosiella. To identify and characterize the clusters, di erent bioinformatics and phylogenetic approaches, as well as PCR-based methods were used. In all genomes studied, two highly conserved NRPS genes (one monomodular and one multimodular) were identified and their potential products were predicted to be siderophores. Expression analysis of two Huntiella species (H. moniliformis and H. omanensis) confirmed the accuracy of the annotations and proved that the genes in both clusters are expressed. Furthermore, a phylogenetic analysis showed that both NRPS genes of the Ceratocystidaceae formed distinct and well supported clades in their respective phylograms, where they grouped with other known NRPSs involved in siderophore production. Overall, these findings improve our understanding of the diversity and evolution of NRPS biosynthetic pathways in the family Ceratocystidaceae.en_ZA
dc.description.departmentBiochemistryen_ZA
dc.description.departmentForestry and Agricultural Biotechnology Institute (FABI)en_ZA
dc.description.departmentGeneticsen_ZA
dc.description.departmentMicrobiology and Plant Pathologyen_ZA
dc.description.librarianam2020en_ZA
dc.description.sponsorshipThe University of Pretoria, the South African National Research Foundation (NRF) and the South African Department of Science and Technology (DST) via the Centers of Excellence program (Center of Excellence in Tree Heath Biotechnology) and the South African Research Chairs Initiativeen_ZA
dc.description.uriwww.mdpi.com/journal/genesen_ZA
dc.description.urihttp://www.mdpi.com/journal/genesen_ZA
dc.identifier.citationSayari, M., Van der Nest, M.A., Steenkamp, E.T. et al. 2019, 'Distribution and evolution of nonribosomal peptide synthetase gene clusters in the Ceratocystidaceae', Genes, vol. 10, art. 328, pp. 1-17.en_ZA
dc.identifier.issn2073-4425 (online)
dc.identifier.other10.3390/genes10050328
dc.identifier.urihttp://hdl.handle.net/2263/75854
dc.language.isoenen_ZA
dc.publisherMDPI Publishingen_ZA
dc.rights© 2019 by the authors. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en_ZA
dc.subjectNonribosomal peptide productionen_ZA
dc.subjectCeratocystidaceaeen_ZA
dc.subjectSiderophore productionen_ZA
dc.subjectNonribosomal peptide synthetase (NRPS)en_ZA
dc.titleDistribution and evolution of nonribosomal peptide synthetase gene clusters in the Ceratocystidaceaeen_ZA
dc.typeArticleen_ZA

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