The complete mitochondrial genome of Trichoderma simmonsii (Hypocreales: Hypocreaceae) from the Southern Coast of Korea

Abstract Fungal species in the genus Trichoderma are widely used for industrial enzyme production and as biocontrol agents. In this study, we report the complete mitochondrial genome of a marine-derived Trichoderma simmonsii strain GH-Sj1, which belongs to the Harzianum clade of Trichoderma. GH-Sj1 was isolated from an edible sea alga Saccharina japonica collected from the southern coast of Korea. This newly assembled circular molecule is 28,668 bp in length and consists of 15 protein-coding genes, 26 transfer RNA genes, and two ribosomal RNA genes. Phylogenetic analysis using the maximum likelihood method shows that T. simmonsii GH-Sj1 is closely related to Trichoderma harzianum and Trichoderma lixii. To the best of our knowledge, this is the first characterization of a marine-derived mitogenome within the genus Trichoderma.

Members of the genus Trichoderma are known to produce commercial enzymes including cellulase and chitinase (di Cologna et al. 2018). In addition, they are utilized in agriculture to control fungal pathogens and promote plant growth (Zin and Badaluddin 2020). Trichoderma simmonsii Chaverri, Rocha, Samuels, Degenkolb, and Jaklitsch 2015, in the family Hypocreaceae, was first identified in the United States and has been reported in Europe and East Asia (Chaverri et al. 2015). Unlike other T. simmonsii strains which were isolated mostly from decaying bark and decorticated wood, the specimen for this study (strain GH-Sj1) was isolated from Saccharina japonica, a very well-known edible sea algae called Kombu. It was collected from Gul-Hang Quay at Sacheon, Gyeongsangnamdo Province, Republic of Korea (34.55 0 43.5 00 N, 128.03 0 24.8 00 E), following the Guideline for Investigations in Marine Life produced by National Marine Biodiversity Institute of Korea (MABIK). Genomic DNA (gDNA) extraction was performed by a phenol-chloroform method, and the fungal isolate and gDNA were deposited at MABIK (https://www.mabik.re.kr, Dawoon Chung, and dwchung@ mabik.re.kr) under voucher number FU00001116.
The complete mitochondrial genome of T. simmonsii GH-Sj1 (GenBank accession MZ292901) is 28,668 bp long, where GC content is 27.6% and the overall base composition of A, C, G, and T is 36.1%, 12.5%, 15.1%, and 36.3%, respectively. The mitogenome harbors 15 protein-coding genes, which start with ATG except for rps3 of ATA. The stop codon for all genes is TAA.
There are 26 transfer RNA (tRNA) genes with lengths ranging from 70 bp to 87 bp. Of these 26 tRNA genes, tRNA Met has three copies, while tRNA Ser , tRNA Phe , tRNA Gln , and tRNA Arg have two copies. Other 15 tRNAs have a single copy. A group of 12 tRNA genes lie between rps3 and nad2. The mitogenome also contains two ribosomal RNA (rRNA), small subunit rRNA (SSU) and large subunit rRNA (LSU), where the lengths of SSU and LSU are 1489 bp and 4709 bp, respectively.
A phylogenetic analysis was performed with mitogenomes of 12 fungal species belonging to the order Hypocreales. The mitochondrial genome of Clonostachys rosea from the family Bionectriaceae was selected as an out-group. A maximum likelihood (ML) tree was constructed using RAxML v8.2.10 (Stamatakis 2014) from 14 single copy orthologous genes with GAMMA-JTT protein substitution model and 100 bootstrapping options, which placed T. simmonsii GH-Sj1 among Hypocreaceae with high bootstrap support values between 72% and 100% (Figure 1). In addition, T. simmonsii GH-Sj1 formed monophyletic clade with T. harzianum, T. lixii and T. reesei. In conclusion, the complete mitogenome of T. sim-monsii GH-Sj1 will provide an important genetic resource and further understanding of mitochondrial evolution in fungi.

Ethical approval
The marine samples collected and used for this study do not involve any marine organisms under protection determined by Ordinance of the Ministry of Oceans and Fisheries in Republic of Korea. Therefore, our study was exempted from the ethical approval and did not need any permissions to carry it out.

Authors' contributions
YMK and DC isolated the sample. DC and YY performed the experiment. YY performed mitogenome analyses. All authors wrote the manuscript. All authors have read and accepted the final manuscript.

Disclosure statement
No potential conflict of interest was reported by the author(s).