Abstract:Background Saccharopolyspora is an important genus of rare actinomycetes. Strain BM8-3, isolated from sediments of the Mariana Trench, exhibits strong salt tolerance and antagonistic activity against pathogens. Currently, studies are limited regarding the functional genes, genomics, and metabolite biosynthesis of Saccharopolyspora from deep sea environments.Objective To analyze the genome sequence and functional genes and evaluate the secondary metabolite synthesis of Saccharopolyspora sp. BM8-3, thus laying a foundation for exploring the strategies of this strain for adapting to extreme environments and mining the gene resources involved in the synthesis of novel secondary metabolites.Methods The whole genome of strain BM8-3 was sequenced on the PacBio platform. Genome assembly was performed by SMRT Link 5.0.1, and gene prediction and functional annotation were conducted with cluster of orthologous groups of proteins (COG) and Kyoto encyclopedia of genes and genomes (KEGG).Results The genome of strain BM8-3 had a total length of 6 344 421 bp, with the G+C content of 72.5%. A total of 5 620 genes, 51 tRNA genes, and 12 rRNA genes were annotated. The annotation against COG and KEGG predicted 4 137 and 2 677 genes, respectively. The genome of strain BM8-3 contained rich genes related to osmotic pressure and high hydrostatic pressure adaptation, including genes involved in the synthesis and transport of compatible solutes such as trehalose (otsAB), glycine betaine (betAB), ectoine (ectABCD), and dimethylglycine/sarcosine (gsmt-sdmt). Additionally, the genome contained genes associated with sodium and potassium ion transport systems (e.g., multiple resistance and pH-related antiporter) and organic solute transport channels (e.g., MscL). Furthermore, the genes associated with cold adaptation were annotated, including cspA encoding cold shock protein, genes encoding the GroEL-GroES chaperonin system, and multiple genes involved in the metabolism of unsaturated fatty acids (e.g., desC and fabF). KEGG annotation revealed that strain BM8-3 possessed a complete taurine transport and metabolism pathway (TauABCD) as well as a thiamine salvage pathway. Additionally, 24 biosynthetic gene clusters (BGCs) for secondary metabolites were predicted in the genome, with more than 50% showing less than 60% similarity to known BGCs. This finding suggested the potential of strain BM8-3 to produce novel secondary metabolites.Conclusion We analyzed the whole-genome sequence of Saccharopolyspora sp. BM8-3, revealing its metabolic diversity and adaptation mechanisms in extreme environments. This study provides critical insights into the environmental adaptation strategies of deep-sea actinomycetes and their roles in sulfur cycling.