Data From: The complete mitochondrial genome of the basidiomycetous fungus, Tinctoporellus epimiltinus strain RS1

Tinctoporellus epimiltinus is well-known as a wood-decaying fungus. In this study, we present the complete mitochondrial genome of this species, identified using next-generation sequencing technology. Our findings reveal that the genome structure is a circular molecule with a size of 51,878 bp. Like most Basidiomycota species, it contains 14 core protein-coding genes, one ribosomal protein (rps3) gene, 26 transfer RNA (tRNA) genes, and small and large ribosomal RNA (rns and rnl) genes. Additionally, we identified seven additional open reading frames (ORFs), including two sequences similar to DNA polymerases, one endonuclease-like sequence, and four hypothetical protein genes. 1) Sample Figure The fungal specimen, identified as Tinctoporellus epimiltinus RS1, was isolated into a pure culture using fungal colony purification techniques. The Sample Figure shows the image of the specimen. 2) Mitogenome map of Tinctoporellus epimiltinus strain RS1 The mitogenome map shows the positions of the 14 core protein-coding genes, one ribosomal protein (rps3) gene, 26 transfer RNA (tRNA) genes, and small and large ribosomal RNA (rns and rnl) genes within the mitochondrial genome. 3) Phylogenetic Tree The phylogenetic tree sheds light on the phylogeny of T.epimiltinus, placing it within the cluster of members of Polyporales. Whithin these species, T. epimiltinus shows a closer relationship with Ganoderma and Trametes. 4) Supplementary Materials Combined Figure 1 Sequences obtained from Sanger sequencing (936 bp) which cover regions connecting both ends of the single contig of the mitogenome (51878 bp). It is to be noted that the contig utilized here is derived from the CLCbio Genome Workbench since we have two different versions of contigs derived from two different softwares which are basically identical in length and sequences. Figure 2 The figure shows the alignment of the Sanger sequences to the mitogenome, validating the circularity of the mitogenome.