Complete genome of Nakamurella sp. PAMC28650: genomic insights into its environmental adaptation and biotechnological potential

The mechanisms underlying the survival of bacteria in low temperature and high radiation are not yet fully understood. Nakamurella sp. PAMC28650 was isolated from a glacier of Rwenzori Mountain, Uganda, which species belonged to Nakamurella genus based on 16S rRNA phylogeny, ANI (average nucleotide identity), and BLAST Ring Image Generator (BRIG) analysis among Frankineae suborder. We conducted the whole genome sequencing and comparative genomics of Nakamurella sp. PAMC28650, to understand the genomic features pertaining to survival in cold environment, along with high UV (ultraviolet) radiation. This study highlights the role of polysaccharide in cold adaptation, mining of the UV protection-related secondary metabolites and other related to cold adaptation mechanism through different bioinformatics tools, and providing a brief overview of the genes present in DNA repair systems. Nakamurella sp. PAMC28650 contained glycogen and cellulose metabolism pathways, mycosporine-like amino acids and isorenieratene-synthesizing gene cluster, and a number of DNA repair systems. Also, the genome analysis showed osmoregulation-related genes and cold shock proteins. We infer these genomic features are linked to bacterial survival in cold and UV radiation. Supplementary Information The online version contains supplementary material available at 10.1007/s10142-022-00937-6.

Nakamurella species have been isolated from different sources (Table 1), and their genomes are held responsible for their survival in different environmental conditions. The type strain of Nakamurella species, Nakamurella multipartita, was isolated from activated sludge acclimated with sugar-containing synthetic wastewater and characterized as a polysaccharide-accumulating Gram-positive coccusshaped strain, whereas Nakamurella antarctica s14-144 1 3 18 Page 2 of 16 was isolated from soil near the Antarctic Peninsula. Nakamurella sp. PAMC28650 was isolated from the glaciers of Rwenzori Mountain in Uganda. The Rwenzori Mountains are situated on the border between the Democratic Republic of Congo and Uganda, and form one of the largest glaciated regions, and the most extensive alpine glacier environment in Africa. Since our strain was isolated from glacier, and due to the extreme environment of the isolated sites, this candidate might be suitable in the field of the biodegradation and production of various industrially relevant compounds (Dumorné et al. 2017).
Glacier regions with extremely harsh environment and subzero temperature are home to several microbiomes. They are a major source for the cold-adapted microorganisms (Anesio et al. 2017). These organisms cope with harsh environmental conditions, like freeze-thaw cycle, nutrient limitations, high amount of salt (salinity), and low temperature (Sakamoto and Murata 2002;Anesio et al. 2017). Besides that, cold-adapted bacteria show structural adjustment of enzymes, cold shock protein expression, membrane fluidity maintenance, presence of compatible solutes, and translation and transcription machinery adaptation to cope with external environment (Barria et al. 2013). Due to these factors, the isolation of the psychrophilic microorganisms may provide information about their unique genomic features, ability to produce different cold-adapted enzymes, and their genetic adaptability. At low temperature, the solubility of oxygen is higher, producing the higher reactive oxygen species (ROS), which provides oxidative stress. Because of this reason, oxidative metabolic pathways such as glycolysis, pentose phosphate pathway, tricarboxylic acid cycle (TCA), and electron transport chain are diminished at cold temperature. However, bacterial adjustment pathways with production of ROS are known, and the underlying molecular mechanism and alternative metabolic pathways in cold environment are not fully covered till now (Piette et al. 2012). CAZymes, on the other hand, might also play a significant role in the survival of the microorganisms in freezing temperature. Polysaccharides, such as glycogen, trehalose, and maltodextrin, are major carbohydrates present in cold-adapted microorganisms, and bacteria with their complete metabolic pathways indicate the ability to conserve energy and its utilization (Han et al. 2021). Psychrophilic microorganisms are also affected by high UV radiation, oxidative stress, and desiccation (Lauritano and Rizzo 2020). Pigments produced by coldadapted microbes are considered as an energy source for the process of combating tools against the oxidative stress, extreme temperature, and safety tool against UV irradiation (Becker-Hapak et al. 1997). Depending upon the concentration and composition, the pigments are visible because of the color such as green (chlorophylls), yellow (xanthophylls), and orange to red (carotenoids) (Anesio et al. 2017) activities. Isorenieratene is a light-harvesting pigment carotenoid and generally synthesized by photosynthetic, green sulfur bacteria (Damsté et al. 2001). Naturally synthesizing microorganisms from cold areas have triggered great interest because of their importance in various industries such as nutraceutical, dairy, textile, cosmetics, and pharmaceutical. Furthermore, such pigments have different functions and may exhibit biotechnological activities differently such as photoprotective function, sunscreen, and antibacterial (Silva et al. 2021). Therefore, genomic study of this microorganism is likely to reveal the mechanisms of their adaptation to such harsh conditions. Recently, with the ease in genome sequencing, complete genome analysis research is plentiful. However, the comparative genomic study of Nakamurella and their environmental adaptation features has not yet been reported. This paper presents the genomic analysis of Nakamurella sp. PAMC28650 isolated from glacier, to determine their environmental adaptation features with regard to carbohydrate metabolism, secondary metabolite production, and DNA repair systems.

Isolation of Nakamurella sp. PAMC28650 and genomic DNA preparation
We received Nakamurella sp. PAMC28650, isolated from the glacier in Mt. Rwenzori, Uganda, from the Korea Polar Research Institute (KOPRI, Incheon, Korea). The 16 s rRNA of Nakamurella sp. PAMC28650 was subjected to EzBioCloud database (Yoon et al. 2017) and confirmed as the Nakamurella species. For complete genome analysis, the genomic DNA of Nakamurella sp. PAMC28650 was extracted using a QIAamp DNA Mini Kit (Qiagen Inc., Valencia, CA, USA). The quantity and purity were determined by spectrophotometry (Biochrome, Libra S35PC, UK). Also, we processed the genome to decide the quality by using A260/A280. The extracted genomic DNA was checked by agarose gel electrophoresis to evaluate its quality and stored at − 20 °C. The strain grew enough cells at 15 °C and then provided genomic DNA.

Genome sequencing and assembly of Nakamurella sp. PAMC28650
Complete genome sequencing of Nakamurella sp. PAMC28650 was obtained by PacBio sequel single-molecule real-time (SMRT) sequencing technology (Pacific Biosciences, Menlo Park, CA, USA). SMRTbell library inserts (20 kb) were sequenced using SMRT cells. Results were generated from raw sequence data of 5,629,850 bp that were assembled de novo by using the hierarchical genome assembly process (HGAP) protocol (Chin et al. 2013) and HGAP4 assembly using SMRT analysis software (ver. 2.3; Pacific Biosciences, https:// github. com/ Pacifi cBio scien ces/ SMRT-Analy sis). The complete genome sequence was deposited in the GenBank database under the GenBank accession number CP060298.1.

Genome annotation of Nakamurella sp. PAMC28650
Genome annotation of Nakamurella species was performed using the Rapid Annotation Subsystem Technology (RAST) server (Overbeek et al. 2014). All the genomes were downloaded using the National Center for Biotechnology Information (NCBI) in fasta format and uploaded to the server. Further, CAZyme analysis was conducted with the help of dbCAN tool (Zhang et al. 2018), and the Kyoto Encyclopedia of Genes and Genomes (KEGG) database (Kanehisa and Goto 2000), used to predict the pathways of cellulose and starch and glycogen metabolism. All the gene-encoding proteins were performed nucleotide BLAST analysis to know the conserved domain in conserved domain database (CDD). Circular map of the genomic DNA was made using the CGView comparison tool (Grant and Stothard 2008). For secondary metabolite gene clusters, genome fasta sequence was submitted to antiSMASH and RAST server, and the result was analyzed.

Phylogenetic placement and comparative genome analysis
For phylogenetic analysis, we compared the genus belonging to Frankineae suborder including Nakamurella genus, using 16S rRNA. All the 16S rRNA sequences were downloaded from the NCBI database. MEGA X was used for the reconstruction of a neighbor-joining tree with 1000 bootstrap replicates (Kumar et al. 2018). We downloaded the complete genome sequences of Frankia suborder species available in GenBank (https:// www. ncbi. nlm. nih. gov). First, the relationship of PAMC28650 with other Frankia suborder species was determined by comparing the value of average nucleotide identity (ANI), calculated using an OrthoANI in the Orthologous Average Nucleotide Identity Tool (OAT) (Lee et al. 2016). Three closely related Nakamurella spp. were selected for CAZyme analysis, and genes were reannotated by the DBCAN2 server. In addition, genome alignment of PAMC28650 was performed using BLAST Ring Image Generator (BRIG) (Alikhan et al. 2011).

Results and discussion
Complete genome profile of Nakamurella sp. PAMC28650 Nakamurella sp. PAMC28650 has a circular chromosome of 5.63 Mb, as shown in Fig. 1A. It contains high GC percentage (67.9%). In this strain, the predicted protein-coding genes are total of 4888 including hypothetical protein. The predicted total numbers of tRNA and rRNA are 47 and 6, respectively, with Scaffold 1 ( Table 2).
The complete genome sequence of Nakamurella sp. PAMC28650 was subjected to RAST annotation server. The RAST subsystem is a manually curated SEED database and is therefore one of the most important bioinformatics tools used (Overbeek et al. 2014). RAST annotation categorizes the genes into two groups: either in the subsystem or not in the subsystem, depending on the protein families with common function. Genes that are categorized in the subsystem are considered reliable and conservative gene predictions. Among 5356 genes, only 20% (290) genes were classified in the subsystem (known functions), while 80% (4323) of genes were not in the subsystem (Table 3). Figure 2 compares the genes belonging to the subsystem between Nakamurella sp. PAMC28650, Nakamurella multipartita DSM44233, and Nakamurella antarctica s14-144. All Nakamurella species showed the highest number of genes in the categories like carbohydrates, amino acids and derivatives, protein metabolism and cofactors, vitamins, prosthetic groups, and pigments. Bacterial stress response (e.g., heat shock and cold shock response) was also an important factor to withstand the extreme surrounding, and therefore, PAMC28650 has the highest proportion of genes as compared to other Nakamurella species.

Phylogenetic tree, ANI, and BRIG analysis of Nakamurella species
The result obtained from EzBioCloud database for 16 s rRNA analysis is shown in Table S1, where the strain shows 99.3% pairwise similarity with Nakamurella panacisegetis. The phylogenetic position of Nakamurella sp. PAMC28650 was analyzed using 16S rRNA sequence of 31 species belonging to Frankineae suborder, including our strain. We included 16S rRNA of all the complete and partial genomes of Nakamurella species. All the Nakamurella species fell in the same clade with a common ancestor, while the closest relative of Nakamurella sp. PAMC28650 was found to be Nakamurella panacisegetis strain P4-7. We can say that this strain belongs to the family Nakamurellaceae and phylum Actinobacteria. Figure 3 shows the phylogenic position of our strain.
Average nucleotide identity (ANI) is another way to determine the relatedness of Nakamurella sp. PAMC28650 strain, by comparison with the complete nucleotide sequences of the species from Frankineae suborder. ANI values were calculated using OrhtoANI in the Orthologous Average Nucleotide Identity Tool (OAT) with cutoff value (95 to 96%) (Lee et al. 2016). Nakamurella sp. PAMC28650 Innermost layer is a Nakamurella sp. PAMC28650 (as a reference sequence) followed by Nakamurella antarctica s14-144 and Nakamurella multipartita DSM 44,233 showed the highest ANI value with Nakamurella multipartita DSM44233 (73.34%) isolated from activated sludge acclimated with sugar-containing synthetic wastewater and Nakamurella antarctica s14-144 (69.81%) from soil (Fig. 4). Based on the ANI value, no significant identity was observed for Nakamurella sp. PAMC28650 among any species in the Frankineae suborder; therefore, it might belong to a new species (Table S4). We had only included Nakamurella multipartita DSM44233 and Nakamurella antarctica s14-144 among the Nakamurella species for ANI calculation, as complete nucleotide sequences of other Nakamurella species were not available in the NCBI. The ANI method is the common method for bacterial comparative genomics. This calculates the average base similarity between two different microbial genomes of homologous fragment at the nucleotide level like the DNA-DNA hybridization method, to identify the relatedness between bacterial species. We also compared the whole genome sequences of the Nakamurella sp. PAMC28650 as a reference strain including Nakamurella multipartita DSM44233 and Nakamurella antarctica s14-14 using BLAST Ring Image Generator (BRIG). BRIG analysis represents the circular genomic map showing the identity between genome of Nakamurella sp. PAMC28650 against Nakamurella antarctica s14-144 and Nakamurella multipartita DSM44233 in a circular ring, colored depending on the BLAST identity (Fig. 1B). This analysis also highlighted that the shared genome and unmatched genome sequences among three species indicating our strain may be a new species. BRIG analysis also supports the result of ANI analysis. Therefore, the Nakamurella sp. PAMC28650 may be a new species.

Comparative CAZyme analysis and carbohydrate metabolism in cold-adapted Nakamurella species
CAZyme analysis was done to find out the carbohydrate metabolism-related genes in Nakamurella sp. PAMC28650 strain. The CAZyme-related genes predicted in this strain are categorized into 6 groups, namely, glycoside hydrolases (GH), glycosyltransferases (GT), polysaccharide lyases (PL), carbohydrate esterases (CE), carbohydrate-binding modules (CBM), and auxiliary activities (AA). Among the 117 CAZyme genes predicted by dbCAN database in PAMC28650 strain, the maximum numbers of genes annotated are in GH families (57), 28 genes in CBM family, 25 genes in GT family, and 2 in AA family (Tables S2 and S3). However, there are no genes classified in PL family. On comparison to Nakamurella multipartita DSM44233 and Nakamurella antarctica s14-144, Nakamurella sp. PAMC28650 contained maximum numbers of GH, CBM, and AA families (Fig. 5). Further analysis of the genome of Nakamurella sp.
PAMC28650 strain for carbohydrate metabolism in KEGG database, genes, and pathways related to glycogen and cellulose metabolism was revealed. Figure 6 and Table 4 show the list of enzymes and their CAZyme classification for cellulose and glycogen metabolism. Glycogen is a homopolysaccharide composed of alpha D-glucose held together by alpha-1,4 and alpha-1,6 glycosidic bond, which is mainly found in animals, fungi, and bacteria, and which acts as a major source of energy storage in bacteria (Wilson et al. 2010 (Table 4). Glycogen heterogeneities support the durable energy storage mechanism hypothesis (DESM) (Wang and Wise 2011), and glycogen with its slow degradation nature means the use of glucose by bacteria at a slow rate, so that bacteria can survive longer time in a starved condition.
Cellulose is a polysaccharide composed of a linear chain of beta D-glucose held together by beta-1,4 glycosidic bond (Updegraff 1969). For the synthesis of cellulose, UDP-glucose is polymerized with the help of enzyme cellulose synthase [EC 2.4.1.12] into long and unbranched chain (beta-1,4 chain) (Klemm et al. 2005). Naturally, bacteria can synthesize cellulose as a protective layer in the cells (Ross et al. 1991). Only Nakamurella sp. PAMC28650 contained cellulose synthase, but the cellulose degradation pathway was present in all the Nakamurella species studied (Fig. 6). Some of the bacterial species, including Gram-positive and Gram-negative bacteria, also produce cellulose (Jonas and Farah 1998). Both plants and bacteria can synthesize cellulose naturally, but their difference is that bacterial cellulose has high purity, and greater water holding capacity, surface area, degree of polymerization (Gorgieva and Trček , as compared to plant cellulose. Another aspect of cellulose biosynthesis in bacteria is that they are responsible for the mechanical and chemical, as well as physiological, protection (R. Rebelo et al. 2018). For the cellulose catabolism, cellulase is the key enzyme, and psychrophilic bacteria are the common bacteria to produce cellulase enzyme (Kasana and Gulati 2011). Cold-adapted microorganisms reside in a low-temperature environment, and in such environment, cellulose synthesis and its utilization considering the large proportion of carbon cycle (Garsoux et al. 2004;Zeng et al. 2006) discovered extracellular cold-active cellulase gene celX in deep-sea psychrotrophic Pseudoalteromonas sp. It typically consists of a catalytic domain (N-terminal; glycoside hydrolase family 5) and a cellulose-binding domain (C-terminal; CBM family 5), with cellobiose serving as the key hydrolysate. Similarly, the role of Cel5G, a psychrophilic cellulase from the Antarctic bacterium Pseudoalteromonas haloplanktis, was studied through protein engineering, where the unusually long flexible linker region was found to enhance catalytic efficiency in the cold region (Sonan et al. 2007). This supports that the cold-adapted cellulase helps bacteria retain metabolic and enzymatic activities in extreme environments by utilizing cellulose (Wang et al. 2019). Cellulase enzyme has diversified function, such as textiles and detergent additives; therefore, its isolation from cold-adapted bacteria and industrial production are quite demanding.
Overall, CAZyme analysis plays an important role in understanding the survival of cold-adapted organisms in extreme environments. Not much research has been conducted that particularly focuses on the survival of organisms in zero and subzero temperature in relation to carbohydrate metabolism. However, carbohydrate's metabolisms, such as starch, glycogen, and trehalose metabolisms, are known as sources of energy for cold-tolerant microorganisms (Han et al. 2021). Another recently published paper also highlighted the importance of cellulose and hemicellulose metabolism for survival in harsh environment (Shen et al. 2021). During extreme environment, primary metabolism is diminished in bacteria, and very little energy is generated using carbohydrates. Both catabolism and anabolism are necessary to store and generate the energy for the survival of cold-residing microorganisms.

Osmotic stress regulatory genes present in Nakamurella sp. PAMC28650
Bacteria reside different environmental conditions with continuous changing physical properties such as temperature, salinity, and osmolarity. Despite the variation in the external environment, microorganisms have to maintain cytoplasmic hydration for their growth and survival. Osmotic stress from the environment is one of the important factors that determine the ability of any microorganism to proliferate in its habitat. Osmotic stress implies an increase or decrease in the osmolarity of the environment of an organism, and organisms carry out the primary regulatory process to prevent it. To a high osmotic environment, the main response of bacteria is to accumulate various solutes such as potassium, glutamate, trehalose, proline, and glycine betaine at a concentration that is nearly equal to the osmolarity of the medium (Csonka 1989). The accumulation of compatible solutes can be achieved by either synthesis and/or transportation to maintain the structure of biological macromolecules. Multiple osmoregulatory transporters such as overlapping energy-coupling mechanisms, substrate specificity, and mechanosensitive channels are known to cope osmotic stress (Sukharev et al. 1997;Wood 1999;Booth and Louis 1999). Aquaporins are an osmotically inducible protein released in an osmoregulatory response, which is required for growing cells. Production of glycerol uptake facilitator proteins are also known to be in the response to osmotic pressure (Ben-Amotz and Avron 1973). Other important aspects of osmoregulation are betaine biosynthesis and choline-betaine uptake from the bacterial cell membranes. Glycine betaine biosynthesis is a two-step process (precursor is choline), and it is considered a very effective compatible solute against cold stress protectant. Alternatively, there are various types of glycine betaine transporters, such as OpuA, OpuC, and OpuD, in different bacteria, which helps to accumulate the solutes against osmotic stress (Hoffmann and Bremer 2011).
Nakamurella sp. PAMC28650 inherits five genes related to the osmoregulation, whereas Nakamurella multipartita DSM44233 and Nakamurella antarctica s14-144 contain one and two, respectively. Similarly, choline, betaine uptake, and betaine synthesis genes are also present in Nakamurella sp. PAMC28650. Generally, betaine biosynthesis requires two genes such as BetA (choline dehydrogenase) and BetB (betaine aldehyde dehydrogenase) for the synthesis of glycine betaine. BetA and BetB genes are present in both Nakamurella sp. PAMC28650 and Nakamurella antarctica s14-144 strains, but absent in Nakamurella multipartita DSM44233. Similarly, three different SOX related to sarcosine oxidase subunit genes are also present in both Nakamurella species except Nakamurella antarctica s14-144. Glycine betaine transporters OpuA three genes are present in our strains; however, Nakamurella multipartita DSM44233 contains one ProU gene. Overall, the number of genes is higher in Nakamurella sp. PAMC28650 compared to other Nakamurella strains (Table 5).

Cold shock protein-related genes present in Nakamurella PAMC28650
A number of mechanisms are involved in microorganisms for adapting with various extreme environmental conditions for the microbial survival. Temperature is one of the key environmental factors affecting growth and the survival of microorganisms (Richter et al. 2010). Bacteria produce small cold shock proteins (multifunctional RNA-DNAbinding proteins) to counteract harmful effect of temperature downshift (Graumann and Marahiel 1996). Cold shock proteins (Csps) have been reported in psychrophilic, mesophilic, and even hyperthermophilic bacteria. Till now, only CspA, CspB, CspE, CspG, and Cspl proteins were induced from the Escherichia coli by cold shock (Jin et al. 2014). Cell membrane homeostasis and activity of enzyme diminish in bacteria during cold shock, and this will ultimately reduce the efficacy of transcription and translation. Furthermore, the protein folding and function of ribosome are disturbed. Csps generally bind to both DNA and RNA to monitor the transcription process by promoting the formation of single-stranded RNA. It also enhances the translation of proteins through CspA, which helps to facilitate the selection of translation at low temperature (Keto-Timonen et al. 2016). In the Nakamurella sp. PAMC28650, three genes encoding two CspA and one CspE were categorized by the RAST analysis (Table S5). CspA is reported as the major shock protein whereas CspE has been reported for the regulation and expression of cold response protein. These genes share high similarity of more than 57% with the known Csps from the UniProt database. Like other different cold adaptational feature analyzed by genome analysis tool, these Csps might have role in adaptation in such harsh condition.

Secondary metabolite gene cluster in Nakamurella sp. PAMC28650 and their relevance to UV resistance
Secondary metabolites, which are not normally involved in cellular function such as growth, adhesion, development, and reproduction, are the organic compounds synthesized by plants, fungi, and bacteria. Bacteria produce different kinds of secondary metabolites during their stationary phase, because of nutritional deficient to overcome the environmental stress (Ruiz et al. 2010). Nakamurella sp. PAMC28650 was isolated from Mt. Rwenzori, Uganda, where evidence suggests a very high UV radiation impact on lakes in the Rwenzori Mountains. We analyzed the genome of Nakamurella sp. PAMC28650 along with other Nakamurella species to find genes related to secondary metabolites using RAST annotation server (Table S5) and antiSMASH. The secondary metabolite gene clusters distributed among all the species are shown in Table S6 and Fig. S1. PAMC28650 was found to contain gene cluster for the synthesis of isorenieratene and mycosporine-like amino acid (MAA). Both the metabolites are responsible for the protection of microorganisms from environment subjected to high UV radiation (Bhatia et al. 2011;Chen et al. 2019). Carotenoids are an important group of isoprenoid units, having a characteristic of conjugated tetraterpenes (C40). Its color ranges from red, yellow, orange, and colorless. Light-absorbing chromophores present in carotenoids play a crucial role in preventing UV radiation to the cells as well as showing antioxidant  (Wang et al. 2019). Briefly, a carotenoid molecule may exchange electronic energy during energy quenching and change into triplet oxygen. Under these changes, it can easily prevent the oxidation reaction (Frank and Brudvig 2004). Isorenieratene is a light-absorbing carotenoid pigment produced by bacteria, fungi, and algae including plants (Yamaguchi 1959). It is an aromatic compound like beta-carotene, having two Φ rings that contribute to its better stability against oxidative stress. Benzene ring has been especially highlighted for UV resistance feature (Martin et al. 2009;Chen et al. 2018). Nakamurella sp. PAMC28650 possessed gene cluster for isorenieratene biosynthesis, where 87% of its genes show similarity with the already characterized isorenieratene gene cluster of Streptomyces argillaceus and similar percentage of gene similarity with carotenoid gene cluster of Streptomyces griseus subsp. griseus NBRC13350, as shown in Fig. 7. Figure 7 details all of the related enzymes and their gene cluster. Extremophilic bacteria, such as Deinococcus-Thermus group, Bacillus genus, and mesophilic bacteria, namely, Escherichia coli, have been studied to understand the role of carotenoids in UV resistance (Yoon et al. 2009;Tian and Hua 2010). Mycosporine and MAAs are the small pigment, watersoluble molecules that are generally present in high volume of sunlight. The nucleus of mycosporine-like amino acids is 5-dihydroxy-5-hydroxymethyl cyclohex-1,2-ene ring, with a methoxy group at C-2. Various microorganisms, cyanobacteria, and eukaryotes (fungi, yeast, and microalgae) synthesize them. Some bacteria and actinomycetes are also known to produce mycosporine. Actinosynnema mirum DSM43827 and Pseudonocardia sp. strain P1, a first report on Grampositive bacteria to produce mycosporine, show lesser evidence of mycosporine and MAA biosynthesis in bacteria (Miyamoto et al. 2014). As shown by the RAST annotation server, Nakamurella sp. PAMC28650 was found to contain gene cluster for MAA biosynthesis. However, the other two Nakamurella multipartita DSM44233 and Nakamurella antarctica s14-144 lacked the genes. We hypothesize the absence of the gene cluster in the other two species resemble its isolated site, where only Nakamurella sp. PAMC28650 was isolated from extreme environment, referring to extreme cold and UV radiation. The enzymes and gene cluster are shown in Fig. 8, where Nakamurella sp. PAMC28650 shows exact similarity with the gene cluster of a cyanobacteria Nostoc punctiforme ATCC29133 and actinomycetes like Actinosynnema mirum DSM43827 and Pseudonocardia sp. P1.
Overall, the secondary metabolite gene clusters in Nakamurella sp. PAMC28650 signifies its environmental adaptation strategies, but they also carry biotechnological importance. Isorenieratene may ease age-related macular degeneration (AMD) (Chen et al. 2019). Likewise, 3,3′-dihydroxyisorenieratene and isorenieratene are known to help prevent DNA damage in human cells (Martin et al. 2009). MAA structure is composed of cyclohexanone core having two amino acids present in the C1 and C4 positions. In C1 position, amino group is always present while in C4 Fig. 7 Putative isoreineratene biosynthetic gene cluster of Nakamurella sp. PAMC28650, compared with other already characterized bacterial species. Gray color denotes that the genes do not present in Nakamurella sp. PAMC28650 gene cluster position, it is substituted by an oxo or an imino moiety that determine the absorption of UV rays. It can dissolve the energy with production of heat without generating ROS (Singh et al. 2021). On the other hand, MAAs are not only known to prevent UV radiation, but also serve as antioxidant, salt stress tolerance, and nitrogen reservoir (Oren and Gunde-Cimerman 2007). Due to photoprotective activity, mycosporine and MAAs are widely used in cosmetics and skin care purposes.

DNA repair systems in Nakamurella species
Based on the isolation environment of Nakamurella sp. PAMC28650, our study was directed towards understanding the DNA repair mechanisms. UV radiation can easily damage the DNA in a variety of organisms, including humans. However, bacterial cells may develop different types of DNA repair systems to prevent the UV-induced lesion. Table 6 presents the pathway related to UV-damaged DNA repair systems in Nakamurella sp. PAMC28650.
Several studies have reported multiple kinds of DNA repair systems to exist in bacteria. Excision repair systems, including base excision repair (BER), nucleotide excision repair (NER), and mismatch repair (MMR), are the major repair systems in various microorganisms that function by producing glycosylases and polymerases. Other mechanisms include recombination repair, mutagenic repair, and apoptosis. The photolyase-mediated DNA repair system is responsible for the protection of bacterial cells released during photoactivation (Yi and He 2013). We found genes for BER, NER, mismatch repair, and homologous recombination in Nakamurella sp. PAMC28650 based on KEGG analysis.
BER system helps protect the bacterial cells from endogenous DNA damage. DNA damage may be caused by hydrolysis or reactive oxygen species (ROS), or UV radiation or strong alkylating agents (Seeberg et al. 1995). Glycosylases are the key enzyme that helps to remove the degraded bases and endonucleases by binding the apurinic/ apyrimidinic site (AP site) and breaking the glycosidic bond at DNA 5′ to the abasic site, and DNA polymerases repair it (Dalhus et al. 2009).
NER removes the DNA-distorting lesion ranging from small lesion to large. In bacteria, NER systems involve three different genes (UvrABC present in E. coli), which help to recognize the damage, cleave the target site, and carry out the completion of the repair system. The genes like UvrA and UvrB are the energy-independent factors that recognize the lesion, and UvrC and UvrD play the role of the removal of damaged DNA, showing nuclease and helicase activity, respectively. Nakamurella sp. PAMC28650 has all the homologous genes related to UvrABCD repair systems and may play a role in the UVresistant mechanism (Crowley et al. 2006).
The MMR system is activated when the DNA damage is caused by mutation due to error in replication. MutL, MutS (mismatch recognition), and MutH (incision of mismatch strands) genes are mainly responsible for the repair of distorted DNA. However, these three genes are absent in our PAMC28650 strain; however, UVRD helicase II, Exo VII exonucleases, SSB, and DpoIII that play a role in DNA resynthesis, and finally Lig for the ligation of DNA strand, are present.
Homologous recombination is a common pathway for the maintenance and repair of DNA. RecFOR and RecBC are the major pathways for the homologous recombination. Acinetobacter baumannii RecA protein played a role in SOS mutagenesis and protection from UV radiation, as well as other stresses, such as oxidative agents and different types of antibiotics (Aranda et al. 2011). Nakamurella

Conclusions
This study presents the complete genome analysis of Nakamurella sp. PAMC28650 isolated from the glacier of Mt. Rwenzori, Uganda. We isolated the bacteria under laboratory condition and confirmed that the isolated was Nakamurella species depending on the 16S rRNA sequences.
The genome analysis showed that the strain possessed several genes related to carbohydrate metabolism, UV resistance, and osmoregulation, which might play an important role in stress management in an extreme environment like glacier. A complete genome analysis suggests that PAMC28650 has a glycogen and cellulose metabolism pathway associated as CAZyme genes. Additionally, isoreineratene (carotenoid) and mycosporine-like amino acid (MAA), the major secondary metabolites that help in the protection against UV radiation, were found in Nakamurella sp. PAMC28650. Along with it, the strain also holds the genes responsible for osmotic stress regulation, which is one of the major stress conditions in a cold environment. Overall, we expect that the information provided in this study provides a research scope for understanding of the bacterial ability to withstand extreme cold environment, UV-resistant mechanisms, and osmotic stress with respect to polysaccharide metabolism, secondary metabolite biosynthesis, and osmoregulation. In addition, the highlighted features and genes also show the biotechnological importance of the strain Nakamurella sp. PAMC28650.
Author contribution TJO designed and supervised the project. LP, NG, SRH, HP, SHJ, and TJO wrote the manuscript. All authors discussed the results, commented on the manuscript, and approved the manuscript.
Funding This research was a part of the project titled "Development of potential antibiotic compounds using polar organism resources (20200610, KOPRI Grant PM22030)," funded by the Ministry of Oceans and Fisheries, Korea.

Data availability
The complete genome sequence data that support the findings of this study are openly available in GenBank of NCBI at https:// www. ncbi. nlm. nih. gov/, and the deposited GenBank accession number is CP060298.1.

Declarations
Ethics approval and consent to participate Not applicable.

Competing interests
The authors declare no competing interests.
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