Supplementary 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/).
Supplementary 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.
Supplementary 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.
Supplementary file S4. The tables below show the predicted nonribosomal peptide synthetase
(NRPS) gene clusters predicted by SMURF (secondary metabolite unique regions finder) (22; 37).
Supplementary
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.
Supplementary
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.