Comparative Genomic Analysis of Arctic Permafrost Bacterium Nesterenkonia sp. PF2B19 to Gain Insights into Its Cold Adaptation Tactic and Diverse Biotechnological Potential
by
and
Purnima Singh
1, 
Neelam Kapse
2,3,
Vasudevan Gowdaman
2,
Masaharu Tsuji
4,
Shiv Mohan Singh
5,*
and
Prashant K. Dhakephalkar
2,3,* 1
Parvatibai Chowgule College of Arts and Science, Goa 403602, India
2
Maharashtra Association for Cultivation of Science, Agharkar Research Institute, G.G. Agarkar Road, Pune 411004, India
3
Savitribai Phule Pune University, Ganeshkhind Rd., Pune 411007, India
4
Department of Materials Chemistry, National Institute of Technology, Asahikawa College, Hokkaido 071-8142, Japan
5
Department of Botany, Institute of Science, Banaras Hindu University, Varanasi 221005, India
*
Authors to whom correspondence should be addressed.
Sustainability 2021, 13(8), 4590; https://doi.org/10.3390/su13084590
Submission received: 3 March 2021
/
Revised: 15 April 2021
/
Accepted: 15 April 2021
/
Published: 20 April 2021
(This article belongs to the Special Issue Microbial Diversity in Cold Environments and Their Sustainable Use)
Abstract
:Nesterenkonia sp. PF2B19, a psychrophile was isolated from 44,800-year-old permafrost soil. This is the first report on comparative genomics of Nesterenkonia sp. isolated from Arctic. Genome of PF2B19 exhibited the presence of a vast array of genetic determinants involved in cold adaptation i.e., response to cold-associated general, osmotic, and oxidative stress. These genomic attributes proved to be valuable in unraveling the adaptive tactics employed by PF2B19 for survival in the cold permafrost soils of the Arctic. Genomic analysis of PF2B19 has given some valuable insight into the biotechnological potential of this strain, particularly as a source of cold-active enzymes, as a bioremediating agent and as plant growth-promoting bacteria.
1. Introduction
Permafrost defines soil, rock or sediment that is frozen for more than two consecutive years [1], covering >25% of the land surface in the northern hemisphere [2]. Harsh conditions prevail in such soils like nutrient limitation, extreme aridity and pH, low temperature, high ultraviolet irradiation, etc. [3,4]. In spite of such extreme conditions, reports suggest the presence of metabolically-active microbial life in the permafrost soil of Svalbard [5,6]. Permafrost soils are considered as chronological collections of past and present microbes [7]. These soils are characterized as extreme environments which can severely impair the cellular function by negatively affecting the cell integrity, membrane fluidity, enzyme kinetics and other interactions [8]. Therefore, for an organism to survive and grow in such extreme niches, it should harbor genes encoding enzymes involved in regulation of DNA replication, transcription, translation and membrane fluidity at low temperatures and other stress combative mechanisms. The microorganisms harboring such harsh microenvironments have evolved certain adaptive features to combat various cold environment-related stresses such as cold stress, oxidative stress, osmotic stress, low nutrient availability, etc. [9,10].
In the last few decades, there has been a growing interest in permafrost as it is known to harbor potentially novel and biotechnologically important microorganisms [11]. Psychrophiles are the most probable sources of cold-active enzymes [12]. These cold-active enzymes have high catalytic efficiency and stability at low and moderate temperatures [13]. Cold-active enzymes have huge market potential as compared to mesophilic and thermophilic enzymes as they shorten process time and cut down energy costs. These enzymes find wide applications in biotechnological and industrial usage, especially in detergents, cosmetics, textiles, etc.
Although permafrosts are known to cover 27% of the Earth [14], there are very few reports on bacterial community composition of permafrost soil from Svalbard (78 °N) [15,16]. Additionally, genomes sequenced from cold environments are relatively few [17]. The molecular strategy employed by bacteria for cold-adaption in such harsh environments remains poorly understood. Genus Nesterenkonia belongs to the family Micrococcaceae, within the phylum Actinobacteria [18]. Nesterenkonia sp. is coccoid, aerobic and non-spore forming bacteria [18,19]. At present, only nine genomes of Nesterenkonia, sp. are available publicly. Reports suggest that some of the Nesterenkonia strains are associated with extreme environments underlining their importance as sources of industrially important cold active enzymes [20].
In this study, a psychrophilic bacterium, Nesterenkonia sp. strain PF2B19 was isolated from permafrost soil. Here, we attempted, by means of genome sequencing of this strain, to unravel the molecular machineries associated with cold adaptation and to identify industrially important cold-active enzymes.
2. Materials and Methods
2.1. Sampling Site, Bacterial Strain and Growth Conditions
Nesterenkonia sp. PF2B19 (PF2-B6) was isolated from permafrost soil gathered from Svalbard, Arctic (78°55.165′ N, 11°52.660′ E) on 20 August 2007. This strain was cultured routinely at 15 °C on Zobell Marine Agar. The pure culture of Nesterenkonia sp. PF2B19 has been deposited with accession number MCC 3408 at Microbial Culture Collection (MCC), India.
2.2. Genomic DNA Preparation and Genome Sequencing
Genomic DNA from the strain PF2B19 was isolated using GenElute™ Bacterial Genomic DNA Isolation kit (Sigma, St. Louis, MO, USA). The PF2B19 genome was sequenced on the Ion Torrent PGM platform (Life Technologies, Carlsbad, CA, USA) using the 316™ chip and 200-bp chemistry. The obtained sequence was then de novo assembled using SPAdes assembler version 3.9.1 [21].
2.3. Comparative Genomics
Digital DNA-DNA Hybridization was executed as described by Auch et al. (2010) [22] using online tool http://ggdc.dsmz.de (accessed on 3 March 2021) with PF2B19 as query genome and Nesterenkonia JCM 19054, Nesterenkonia alba DSM 19423(T), Nesterenkonia massiliensis strain NP1, Nesterenkonia sp. AN1, Nesterenkonia sp. F and Nesterenkonia jeotgali CD08_7 as reference genomes. Genome sequence of PF2B19 further compared with the genomes of above mentioned strains in RAST tool to determine distinctive genomic determinants, i.e., gene unique in PF2B19 to prove its novelty. A circular map representing the general genome comparisons of strain PF2B19 with its close phylogenetic affiliates (Nesterenkonia JCM 19054, Nesterenkonia alba DSM 19423(T) and Nesterenkonia sp. AN1) was generated using the BRIG program. BRIG uses BLAST for genome comparisons and CGView for image generation. The circular image is generated wherein the reference genome is placed at the center and other query genomes as a set of concentric rings colored displaying similarity. The genomes of reference Nesterenkonia strains NP1, F, AN1, JCM 19054, DSM 19423 and CD08_7 were obtained from the NCBI database.
2.4. Functional Annotation
Functional annotation of PF2B19 genome was carried out by Rapid Annotation using Subsystem Technology (RAST) [23]. PF2B19 genome was mined for the presence of genes having role in cold adaptation and biotechnological potential in RAST annotation tool. Pathway elucidation was executed using Kyoto Encyclopedia of Genes and Genomes (KEGG) (http://www.genome.ad.jp accessed on 3 March 2021) database. Virulence determinants were detected using the online tool Virulence Finder [24].
2.5. Accession Nnumber
The Nesterenkonia sp. PF2B19 whole Genome Shotgun project has been deposited at GenBank under the accession no. MDSS00000000.
3. Results and Discussion
3.1. Characterization and Phylogeny of PF2B19
PF2B19, a Gram positive, strictly aerobic coccoid, was identified as the affiliate of the psychrophilic genus Nesterenkonia based on 16S rRNA gene sequencing, displaying maximum 16S rRNA sequence (1312 nucleotides) homology of 99% with closest phylogenetic neighbors Nesterenkonia aethiopica DSM 17733(T), Nesterenkonia xinjiangensis strain YIM70097, Nesterenkonia sp. YIM70097 and Nesterenkonia suensis Sua-BAC020(T). PF2B19 shared 98% homology with Nesterenkonia massiliensis strain NP1. 16S rRNA gene sequences of PF2B19 were aligned with those of the publicly available Nesterenkonia 16S rRNA sequences using the Mega version 6.0 [25] Phylogenetic tree showing the taxonomic relationship of strain PF2B19 with other Nesterenkonia strains was constructed by employing the neighbor-joining algorithm (Figure 1).
However, the whole genomes of Nesterenkonia aethiopica DSM 17733(T), Nesterenkonia xinjiangensis strain YIM70097, Nesterenkonia sp. YIM70097 and Nesterenkonia suensis Sua-BAC020(T) are not available in the NCBI database, so Nesterenkonia JCM 19054, Nesterenkonia alba DSM 19423(T), Nesterenkonia massiliensis strain NP1, Nesterenkonia sp. AN1, Nesterenkonia sp. F and Nesterenkonia jeotgali CD08_7 were selected for Digital DNA–DNA hybridization. Digital DNA–DNA hybridization revealed homology of only 27.50%, 23.10%, 24.90%, 24.50%, 26.30% and 24.70% between PF2B19 and Nesterenkonia JCM 19054, Nesterenkonia alba DSM 19423(T), Nesterenkonia massiliensis strain NP1, Nesterenkonia sp. AN1, Nesterenkonia sp. F and Nesterenkonia jeotgali CD08_7 respectively, outlining the difference between the species and also illustrating the novelty of strain PF2B19. Based on this information, PF2B19 can be considered as a putative novel species of the genus Nesterenkonia.
3.2. General Genome Features of Permafrost Bacterium Nesterenkonia sp. PF2B19
Sequencing of the library generated 3,698,032 bp reads, which were de novo assembled using SPAdes assembler version 3.9.1 into 135 contigs, yielding a 3.6 Mb genome with 69.5% G+C content. These results were in congruence with publicly available draft genomes of three strains of Nesterenkonia possessing sizes in the range of 2.59 to 3.01 Mb and G+C contents of 62.2 to 71.5%. Functional annotation pf PF2B19 genome by RAST revealed a total of 3763 proteins were predicted, including 3708 coding sequences and 55 total RNAs. Differentiating genome features of query genome PF2B19 along with five reference genomes are illustrated in Table 1.
3.3. General Genome Comparisons of PF2B19 with Its Closest Phylogenetic Affiliates
PF2B19 genome was compared with the available Nesterenkonia genomes, by running BLASTn in BRIG software [26]. The circular map (Figure 2) represents the BLASTn results of each query genome (Nesterenkonia JCM 19054, Nesterenkonia alba DSM 19423(T) and Nesterenkonia sp. AN1) against the reference PF2B19. As evident from the BRIG image, gaps were more pronounced in the query genomes, emphasizing the difference between PF2B19 and the other Nesterenkonia genomes.
3.4. Comparative Genomics Identifies Unique Genes/Proteins in Nesterenkonia sp. PF2B19
Genome annotation performed using RAST tool identified Renibacterium salmoninarum ATCC 33209 (Genome id: 288705.3, Score: 512) as the closest phylogenetic neighbor of PF2B19. On comparative analysis with ATCC 33209, 378 unique genes associated with a subsystem in PF2B19 were detected in PF2B19. These genes were scored as distinctive genomic determinants that differentiated PF2B19 from its phylogenetic associates.
PF2B19 genome was also compared with other Nesterenkonia genomes in RAST. Unique genes were detected in PF2B19 as compared to other Nesterenkonia sp., further highlighting the novelty of PF2B19 (Table 2).
3.5. Identification of Virulence Determinants
No virulent genes were detected in the genome of PF2B19 as revealed by Virulence Finder. Thus, PF2B19 was non-pathogenic.
3.6. Genes Involved in Resistance to Antibiotics
Antibiotic-resistance genes are potentially transferable genes in specific niches such as intestinal microflora where microbial inhabitants are often exposed to an exhaustive use of antibiotics. Yet, current studies have revealed the presence of antibiotic-resistant genes and/or antibiotic-resistance bacteria in the geographically isolated natural niches which are not exploited by anthropogenic factors [27,28,29,30]. We screened the genome of PF2B19, which was isolated from Arctic for presence of antibiotic-resistance genes. Interestingly, genes conferring resistance to fluoroquinolones and Beta lactam group of antibiotics were detected in PF2B19 genome. Presence of mutant genes: DNA gyrase subunit B (gyrB) (EC 5.99.1.3) and DNA gyrase subunit A (gyrA) (EC 5.99.1.3) and Topoisomerase IV subunit A (EC 5.99.1.-) and Topoisomerase IV subunit B (EC 5.99.1.-) were thought to be involved in conferring resistance against fluoroquinolone, while mutant Beta-lactamase class C and other penicillin-binding proteins were responsible for resistance towards Beta lactam group of antibiotics. Svalbard, Arctic, is not yet exploited by anthropogenic activities and the presence of antibiotic-resistance genes in the bacteria isolated from such a pristine environment was quiet surprising. Most probable modes of transmission would be through airborne bacteria and migratory birds.
Arctic is characterized by harsh cold conditions. The stresses encountered by bacteria in permafrost soil include limited nutrients, desiccation, oxidative stress, osmotic stress and persistent low temperatures [31,32]. A repertoire of adaptive genes associated with diverse stresses present in cold milieus have been reported in the literature [33,34,35,36,37]. PF2B19 genome was mined for the adaptive genes that may be associated with survival of PF2B19 in the permafrost soils of Svalbard. Analysis of Nesterenkonia sp. PF2B19 genome revealed a total of 128 putative stress response genes, including 16 genes linked to cold stress response, 16 genes for DNA repair, 12 genes for modulation of membrane fluidity, 39 genes for oxidative stress response, 37 genes for osmotic stress response and 4 in response to general stress (Table 3).
3.6.1. Cold Stress Response
Cold shock proteins are vital for the cold acclimation of bacteria [38]. Cold shock proteins (Csps) serve as nucleic acid chaperons, which counteract the harmful effects of cold stress like inefficient protein folding by regulating transcription and translation at low temperatures [39,40]. Csps have also been known to contribute to various environmental stress tolerance such as osmotic, oxidative, starvation and pH stress. PF2B19 genome contains genes encoding the cold shock proteins CspA and CspC and an arsenal of chaperones like dnaJ, dnaK and grpE, which are considered pivotal for preserving the integrity and function of proteins [41]. The genome also contains genes encoding the secondary CSPs polyribonucleotide nucleotidyltransferase (PNPase), ribosome binding factor A (RbfA), transcription elongation protein (NusA), and translation initiation factor (Inf2) which are typically induced via transcription anti-termination [42].
Modulation of membrane fluidity is crucial for cell viability at lower temperatures. This is achieved by improved production of unsaturated fatty acids, alteration of fatty acid branched chains and shortening of fatty acyl chains [43,44,45]. The Nesterenkonia sp. PF2B19 genome encodes five proteins involved in fatty acid biosynthetic pathways (Table 3). These include FabG and FabH involved in fatty acid biosynthesis, the condensation of fatty acids and the synthesis of branched fatty acids [35,46]. The genome also codes for 1-acyl-sn-glycerol-3-phosphate acyltransferase (PlsC), catalyzing the phospholipid synthesis, and 3-ketoacyl-(acyl-carrier-protein) reductase, involved in enhancing the production of polyunsaturated lipids [35,46]. Additionally, the pathway for unsaturated fatty acid synthesis was detected in PF2B19 using KEGG pathway tool.
3.6.2. Oxidative Stress Response
Bacteria-harboring cold environments are more inclined to the deleterious effects of reactive oxygen species (ROS) because of better solubility of gases at low temperatures [45,50]. Nesterenkonia sp. PF2B19 encoded genes involved in detoxification of ROS such as catalase (kat), two superoxide dismutases (SodA; SodC), a thiol peroxidase (Bcp) as well as thioredoxin and thioredoxin reductase (TrxA and TrxB) [51]. Two putative dioxygenases were also detected in PF2B19 genome, known to play a key role in combating ROS damage [34].
3.6.3. Osmo-Protection
Accumulation of compatible solutes is an effective tactic to combat osmotic stress. These solutes are known to have dual response in stress as osmolytes and cryo-protectants [52]. Nesterenkonia sp. PF2B19 genome encodes a range of proteins involved in combating osmotic stress (Table 2). The genome also encodes transporters for glycine/betaine and choline dehydrogenases which are well-known osmo-protectants [53]. A number of genes involved in the endogenous synthesis of compatible solutes like trehalose biosynthesis genes otsA and otsB, known to be cold-inducible and essential for low temperature survival, were also detected.
3.6.4. General Stress Response
In addition to cold, osmotic and oxidative stress response, the PF2B19 genome encoded a repertoire of other stress-related proteins, which was included in general stress response system (Table 2). Ten genes involved in SOS response (cellular response to DNA damage) and DNA repair systems were detected. The genome also encoded universal stress protein, UspA, which is associated with cold acclimation [54].
3.7. Biotechnological Potential of PF2B19
Cold-active enzymes and the microbes producing them are of great biotechnological potential, with applications in detergent-, food-, textile-industry, pharmaceuticals and molecular biology. Psychrophilic enzymes are considered to be a boon to industry because of shorter process intervals, low energy budgets, low enzyme concentration requirement as well as impeding undesired chemical alterations [55]. Annotated genome sequence of PF2B19 revealed the presence of genes involved in production of cold-active enzymes, particularly of α-amylases, proteases, lipases/esterases, β-glucosidase, β-galactosidase and alkaline phosphatase (Table 4).
Furthermore, genes possibly responsible for hydrocarbon degradation were detected. Genes encoding catabolism of benzoate, catechol were found in the genome. Catecholic compounds are the common inter-mediates in aerobic bacterial aromatic compound degradation pathways [56] and extradiol dioxygenases (EDOs) are known to catalyze the ring cleavage of catecholic compounds. EDOs like catechol 2,3-dioxygenase (EC 1.13.11.2), possible dioxygenase and 3-phenylpropionate dioxygenase ferredoxin subunit were detected in PF2B19. Benzoate catabolism genes 2-oxo-hepta-3-ene-1, 7-dioic acid hydratase (EC 4.2.-.-), and benzoate transport protein, 4-hydroxybenzoate transporter were also detected. Presence of these genes highlighted the bioremediation potential of PF2B19 in cold environment. Additionally, the pathway for degradation of catechol was elucidated in PF2B19 using KEGG database (Figure 3).
PF2B19 also possessed the ability to promote plant growth. Genes involved in acetoin production, i.e., acetolactate synthase and zinc-containing alcohol dehydrogenase were identified in the genome. Acetoin is known to promote plant growth by stimulating root formation [57]. 1-aminocyclopropane-1-carboxylate (ACC) deaminase gene (acdS) was also detected. acdS is known to aid the degradation of a plant’s ethylene precursor, thus promoting plant growth [58]. Arctic plants are challenged by various abiotic stressors in their environment, which are known to limit their growth. PF2B19 can form mutualistic relationship with plants growing in the Arctic and promote growth.
Moreover, the genes encoding proteins involved in resistance to heavy metals and toxic compounds (copper, cobalt, zinc, cadmium, mercury, chromium and arsenic) were detected in PF2B19, highlighting the potential of the PF2B19 to adapt to extreme lifestyles.
4. Conclusions
Based on genomic analysis, it can be concluded that Nesterenkonia sp. PF2B19 employs was found to be well-equipped with proteins involved in cold stress as well as modulation of membrane fluidity, osmotic and oxidative stress responses. Nesterenkonia sp. PF2B19 was found to be non-virulent and non-pathogenic. Genomic analysis of the PF2B19 has given valuable insight into the potential role of this strain in bioremediation in a colder environment. The genomic attributes also revealed the strategies adopted by Nesterenkonia sp. PF2B19 to survive in the extreme cold environment of permafrost.
Author Contributions
Conceptualization, formal analyses and methodology by P.S., N.K., V.G. Writing original draft preparation by P.S. and N.K. Resources and Supervision by P.K.D., S.M.S., M.T. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by Science and Engineering Research Board (SERB), Grant No. (PDF/2016/003707), India.
Institutional Review Board Statement
This study did not involve humans or animals. Therefore, there are no ethical and biosafety issues.
Informed Consent Statement
Not applicable.
Data Availability Statement
The data present in this research article will be available for public interest.
Acknowledgments
We are thankful to the Director, ARI for facilities. Purnima Singh is thankful to SERB-DST for financial support (PDF/2016/003707). Neelam Kapse is thankful to CSIR for the financial support (09/670 (0072)/2016-EMR-I). Thanks to the Almighty for driving us to complete this work during the difficult time of COVID-19.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Péwé, T.L. Permafrost. In Encyclopædia Britannica; 2006; Available online: http://0-search-eb-com.brum.beds.ac.uk/eb/article-9108442 (accessed on 9 April 2008).
- Zhang, T.; Barry, R.G.; Knowles, K.; Heginbottom, J.A.; Brown, J. Statistics and characteristics of permafrost and ground-ice distribution in the Northern Hemisphere 1. Polar Geogr. 1999, 23, 132–154. [Google Scholar] [CrossRef]
- Aislabie, J.M.; Chhour, K.L.; Saul, D.J.; Miyauchi, S.; Ayton, J.; Paetzold, R.F.; Balks, M.R. Dominant bacteria in soils of Marble point and Wright valley, Victoria land, Antarctica. Soil Biol. Biochem. 2006, 38, 3041–3056. [Google Scholar] [CrossRef]
- Chan, Y.; Van Nostrand, J.D.; Zhou, J.; Pointing, S.B.; Farrell, R.L. Functional ecology of an Antarctic dry valley. Proc. Natl. Acad. Sci. USA 2013, 110, 8990–8995. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Humlum, O.; Elberling, B.; Hormes, A.; Fjordheim, K.; Hansen, O.H.; Heinemeier, J. Late-Holocene glacier growth in Svalbard, documented by subglacial relict vegetation and living soil microbes. Holocene 2005, 15, 396–407. [Google Scholar] [CrossRef] [Green Version]
- Singh, S.M.; Sharma, J.; Gawas-Sakhalkar, P.; Upadhyay, A.K.; Naik, S.; Bande, D.; Ravindra, R. Chemical and bacteriological analysis of soil from the Middle and Late Weichselian from Western Spitsbergen, Arctic. Quat. Int. 2012, 271, 98–105. [Google Scholar] [CrossRef]
- Friedmann, E.I. Permafrost as microbial habitat. Viable Microorganisms in Permafrost 1994, 21–26,–26. [Google Scholar] [CrossRef]
- Piette, F.; D’Amico, S.; Mazzucchelli, G.; Danchin, A.; Leprince, P.; Feller, G. Life in the cold: A proteomic study of cold-repressed proteins in the Antarctic bacterium Pseudoalteromonas haloplanktis TAC125. Appl. Environ. Microbiol. 2011, 77, 3881–3883. [Google Scholar] [CrossRef] [Green Version]
- Mesbah, N.M.; Wiegel, J. Life at extreme limits. Ann. N. Y. Acad. Sci. 2008, 1125, 44–57. [Google Scholar] [CrossRef]
- De Maayer, P.; Anderson, D.; Cary, C.; Cowan, D.A. Some like it cold: Understanding the survival strategies of psychrophiles. EMBO Rep. 2014, 15, 508–517. [Google Scholar] [CrossRef]
- Willerslev, E.; Hansen, A.J.; Poinar, H.N. Isolation of nucleic acids and cultures from fossil ice and permafrost. Trends Ecol. Evol. 2004, 19, 141–147. [Google Scholar] [CrossRef]
- Margesin, R.; Dieplinger, H.; Hofmann, J.; Sarg, B.; Lindner, H. A cold-active extracellular metalloprotease from Pedobacter cryoconitis—production and properties. Res. Microbiol. 2005, 156, 499–505. [Google Scholar] [CrossRef]
- Kuddus, M.; Ramteke, P.W. A cold-active extracellular metalloprotease from Curtobacterium luteum (MTCC 7529): Enzyme production and characterization. J. Gen. Appl. Microbiol. 2008, 54, 385–392. [Google Scholar] [CrossRef] [Green Version]
- Goordial, J.; Lamarche-Gagnon, G.; Lay, C.Y.; Whyte, L. Left out in the cold: Life in cryoenvironments. In Polyextremophiles; Springer: Dordrecht, The Netherlands, 2013; pp. 335–363. [Google Scholar]
- Hansen, A.A.; Herbert, R.A.; Mikkelsen, K.; Jensen, L.L.; Kristoffersen, T.; Tiedje, J.M.; Finster, K.W. Viability, diversity and composition of the bacterial community in a high Arctic permafrost soil from Spitsbergen, Northern Norway. Environ. Microbiol. 2007, 9, 2870–2884. [Google Scholar] [CrossRef]
- Schostag, M.; Stibal, M.; Jacobsen, C.S.; Bælum, J.; Taş, N.; Elberling, B.; Jansson, J.K.; Semenchuk, P.; Priemé, A. Distinct summer and winter bacterial communities in the active layer of Svalbard permafrost revealed by DNA-and RNA-based analyses. Front. Microbiol. 2015, 6, 399. [Google Scholar] [CrossRef] [Green Version]
- Bakermans, C.; Bergholz, P.W.; Rodrigues, D.F.; Vishnivetskaya, T.A.; Ayala-del-Río, H.L.; Tiedje, J.M. Genomic and expression analyses of cold-adapted microorganisms. In Polar Microbiology: Life in a Deep Freeze; Miller, R.V., Whyte, L.G., Eds.; ASM Press: Washington, DC, USA, 2012; pp. 126–155. [Google Scholar]
- Stackebrandt, E.; Koch, C.; Gvozdiak, O.; Schumann, P. Taxonomic Dissection of the Genus Micrococcus: Kocuria gen. nov., Nesterenkonia gen. nov., Kytococcus gen. nov., Dermacoccus gen. nov., and Micrococcus Cohn 1872 gen. emend. Int. J. Syst. Evol. Microbiol. 1995, 45, 682–692. [Google Scholar] [CrossRef] [Green Version]
- Li, W.J.; Chen, H.H.; Kim, C.J.; Zhang, Y.Q.; Park, D.J.; Lee, J.C.; Jiang, C.L. Nesterenkonia sandarakina sp. nov. and Nesterenkonia lutea sp. nov., novel actinobacteria, and emended description of the genus Nesterenkonia. Int. J. Syst. Evol. Microbiol. 2005, 55, 463–466. [Google Scholar] [CrossRef] [Green Version]
- Shafiei, M.; Ziaee, A.A.; Amoozegar, M.A. Purification and characterization of a halophilic α-amylase with increased activity in the presence of organic solvents from the moderately halophilic Nesterenkonia sp. strain F. Extremophiles 2012, 16, 627–635. [Google Scholar] [CrossRef]
- Bankevich, A.; Nurk, S.; Antipov, D.; Gurevich, A.A.; Dvorkin, M.; Kulikov, A.S.; Pevzner, P.A. SPAdes: A new genome assembly algorithm and its applications to single-cell sequencing. J. Comput. Biol. 2012, 19, 455–477. [Google Scholar] [CrossRef] [Green Version]
- Auch, A.F.; Jan, M.; Klenk, H.P.; Göker, M. Digital DNA-DNA hybridization for microbial species delineation by means of genome-to-genome sequence comparison. Stand. Genom. Sci. 2010, 2, 117–134. [Google Scholar] [CrossRef] [Green Version]
- Aziz, R.K.; Bartels, D.; Best, A.A.; DeJongh, M.; Disz, T.; Edwards, R.A.; Formsma, K.; Gerdes, S.; Glass, E.M.; Kubal, M.; et al. The RAST Server: Rapid annotations using subsystems technology. BMC Genom. 2008, 9, 75. [Google Scholar] [CrossRef] [Green Version]
- Joensen, K.G.; Scheutz, F.; Lund, O.; Hasman, H.; Kaas, R.S.; Nielsen, E.M.; Aarestrup, F.M. Real-time whole-genome sequencing for routine typing, surveillance, and outbreak detection of verotoxigenic Escherichia coli. J. Clin. Microbiol. 2014, 52, 1501–1510. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Tamura, K.; Stecher, G.; Peterson, D.; Filipski, A.; Kumar, S. MEGA6: Molecular evolutionary genetics analysis version 6.0. Mol. Biol. Evol. 2013, 30, 2725–2729. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Alikhan, N.F.; Petty, N.K.; Zakour, N.L.B.; Beatson, S.A. BLAST Ring Image Generator (BRIG): Simple prokaryote genome comparisons. BMC Genom. 2011, 12, 402. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Allen, H.K.; Moe, L.A.; Rodbumrer, J.; Gaarder, A.; Handelsman, J. Functional metagenomics reveals diverse β-lactamases in a remote Alaskan soil. ISME J. 2009, 3, 243–251. [Google Scholar] [CrossRef]
- Dib, J.R.; Weiss, A.; Neumann, A.; Ordoñez, O.; Estévez, M.C.; Farías, M.E. Isolation of bacteria from remote high altitude Andean lakes able to grow in the presence of antibiotics. Recent Pat. Anti-Infect. Drug Discov. 2009, 4, 66–76. [Google Scholar] [CrossRef] [PubMed]
- Thaller, M.C.; Migliore, L.; Marquez, C.; Tapia, W.; Cedeño, V.; Rossolini, G.M.; Gentile, G. Tracking acquired antibiotic resistance in commensal bacteria of Galapagos land iguanas: No man, no resistance. PLoS ONE 2010, 5, e8989. [Google Scholar] [CrossRef] [Green Version]
- Ushida, K.; Segawa, T.; Kohshima, S.; Takeuchi, N.; Fukui, K.; Li, Z.; Kanda, H. Application of real-time PCR array to the multiple detection of antibiotic resistant genes in glacier ice samples. J. Gen. Appl. Microbiol. 2010, 56, 43–52. [Google Scholar] [CrossRef] [Green Version]
- Vincent, W.F. Cold tolerance in cyanobacteria and life in the cryosphere. In Algae and Cyanobacteria in Extreme Environments; Springer: Dordrecht, The Netherlands, 2007; pp. 287–301. [Google Scholar]
- Mueller, D.R.; Vincent, W.F.; Bonilla, S.; Laurion, I. Extremotrophs, extremophiles and broadband pigmentation strategies in a high arctic ice shelf ecosystem. FEMS Microbiol. Ecol. 2005, 53, 73–87. [Google Scholar] [CrossRef]
- Berger, F.; Morellet, N.; Menu, F.; Potier, P. Cold shock and cold acclimation proteins in the psychrotrophic bacterium Arthrobacter globiformis SI55. J. Bacteriol. 1996, 178, 2999–3007. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Médigue, C.; Krin, E.; Pascal, G.; Barbe, V.; Bernsel, A.; Bertin, P.N.; Fang, G. Coping with cold: The genome of the versatile marine Antarctica bacterium Pseudoalteromonas haloplanktis TAC125. Genome Res. 2005, 15, 1325–1335. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Methé, B.A.; Nelson, K.E.; Deming, J.W.; Momen, B.; Melamud, E.; Zhang, X.; Moult, J.; Madupu, R.; Nelson, W.C.; Dodson, R.J.; et al. The psychrophilic lifestyle as revealed by the genome sequence of Colwellia psychrerythraea 34H through genomic and proteomic analyses. Proc. Natl. Acad. Sci. USA 2005, 102, 10913–10918. [Google Scholar] [CrossRef] [Green Version]
- Gao, H.; Yang, Z.K.; Wu, L.; Thompson, D.K.; Zhou, J. Global transcriptome analysis of the cold shock response of Shewanella oneidensis MR-1 and mutational analysis of its classical cold shock proteins. J. Bacteriol. 2006, 188, 4560–4569. [Google Scholar] [CrossRef] [Green Version]
- Riley, M.; Staley, J.T.; Danchin, A.; Wang, T.Z.; Brettin, T.S.; Hauser, L.J.; Land, M.L.; Thompson, L.S. Genomics of an extreme psychrophile, Psychromonas ingrahamii. BMC Genom. 2008, 9, 210. [Google Scholar] [CrossRef] [Green Version]
- Phadtare, S.; Alsina, J.; Inouye, M. Cold-shock response and cold-shock proteins. Curr. Opin. Microbiol. 1999, 2, 175–180. [Google Scholar] [CrossRef]
- Rabus, R.; Ruepp, A.; Frickey, T.; Rattei, T.; Fartmann, B.; Stark, M.; Amann, J. The genome of Desulfotalea psychrophila, a sulfate-reducing bacterium from permanently cold Arctic sediments. Environ. Microbiol. 2004, 6, 887–902. [Google Scholar] [CrossRef]
- Chaikam, V.; Karlson, D.T. Comparison of structure, function and regulation of plant cold shock domain proteins to bacterial and animal cold shock domain proteins. BMB Rep. 2010, 43, 1–8. [Google Scholar] [CrossRef] [Green Version]
- Goordial, J.; Raymond-Bouchard, I.; Zolotarov, Y.; de Bethencourt, L.; Ronholm, J.; Shapiro, N.; Whyte, L. Cold adaptive traits revealed by comparative genomic analysis of the eurypsychrophile Rhodococcus sp. JG3 isolated from high elevation McMurdo Dry Valley permafrost, Antarctica. FEMS Microbiol. Ecol. 2016, 92, 154. [Google Scholar]
- Bae, W.; Xia, B.; Inouye, M.; Severinov, K. Escherichia coli CspA-family RNA chaperones are transcription antiterminators. Proc. Natl. Acad. Sci. USA 2000, 97, 7784–7789. [Google Scholar] [CrossRef] [Green Version]
- Feller, G. Molecular adaptations to cold in psychrophilic enzymes. Cell. Mol. Life Sci. CMLS 2003, 60, 648–662. [Google Scholar] [CrossRef]
- Feller, G.; Gerday, C. Psychrophilic enzymes: Hot topics in cold adaptation. Nat. Rev. Microbiol. 2003, 1, 200–208. [Google Scholar] [CrossRef]
- D’amico, S.; Collins, T.; Marx, J.C.; Feller, G.; Gerday, C. Psychrophilic microorganisms: Challenges for life. EMBO Rep. 2006, 7, 385–389. [Google Scholar] [CrossRef]
- Hoang, T.T.; Sullivan, S.A.; Cusick, J.K.; Schweizer, H.P. β-Ketoacyl acyl carrier protein reductase (FabG) activity of the fatty acid biosynthetic pathway is a determining factor of 3-oxo-homoserine lactone acyl chain lengths. Microbiology 2002, 148, 3849–3856. [Google Scholar] [CrossRef] [Green Version]
- Chintalapati, S.; Kiran, M.D.; Shivaji, S. Role of membrane lipid fatty acids in cold adaptation. Cell. Mol. Biol. 2004, 50, 631–642. [Google Scholar]
- Morgan-Kiss, R.M.; Priscu, J.C.; Pocock, T.; Gudynaite-Savitch, L.; Huner, N.P. Adaptation and acclimation of photosynthetic microorganisms to permanently cold environments. Microbiol. Mol. Biol. Rev. 2006, 70, 222–252. [Google Scholar] [CrossRef] [Green Version]
- Dieser, M.; Greenwood, M.; Foreman, C.M. Carotenoid pigmentation in Antarctic heterotrophic bacteria as a strategy to withstand environmental stresses. Arct. Antarct. Alp. Res. 2010, 42, 396–405. [Google Scholar] [CrossRef] [Green Version]
- Chattopadhyay, M.K. Mechanism of bacterial adaptation to low temperature. J. Biosci. 2006, 31, 157–165. [Google Scholar] [CrossRef]
- Ballal, A.; Manna, A.C. Control of thioredoxin reductase gene (trxB) transcription by SarA in Staphylococcus aureus. J. Bacteriol. 2010, 192, 336–345. [Google Scholar] [CrossRef] [Green Version]
- Welsh, D.T. Ecological significance of compatible solute accumulation by micro-organisms: From single cells to global climate. FEMS Microbiol. Rev. 2000, 24, 263–290. [Google Scholar] [CrossRef]
- Le Rudulier, D.; Strom, A.R.; Dandekar, A.M.; Smith, L.T.; Valentine, R.C. Molecular biology of osmoregulation. Science 1984, 224, 1064–1069. [Google Scholar] [CrossRef]
- Garnier, M.; Matamoros, S.; Chevret, D.; Pilet, M.F.; Leroi, F.; Tresse, O. Adaptation to cold and proteomic responses of the psychrotrophic biopreservative Lactococcus piscium strain CNCM I-4031. Appl. Environ. Microbiol. 2010, 76, 8011–8018. [Google Scholar] [CrossRef] [Green Version]
- Cavicchioli, R.; Charlton, T.; Ertan, H.; Omar, S.M.; Siddiqui, K.S.; Williams, T.J. Biotechnological uses of enzymes from psychrophiles. Microb. Biotechnol. 2011, 4, 449–460. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Smith, M.R. The biodegradation of aromatic hydrocarbons by bacteria. In Physiology of Biodegradative Microorganisms; Springer: Wageningen, The Netherlands, 1991; pp. 191–206. [Google Scholar]
- Ryu, C.M.; Farag, M.A.; Hu, C.H.; Reddy, M.S.; Wei, H.X.; Paré, P.W.; Kloepper, J.W. Bacterial volatiles promote growth in Arabidopsis. Proc. Natl. Acad. Sci. USA 2003, 100, 4927–4932. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Glick, B.R. Bacteria with ACC deaminase can promote plant growth and help to feed the world. Microbiol. Res. 2014, 169, 30–39. [Google Scholar] [CrossRef] [PubMed]
Figure 1.
Phylogenetic tree displaying the taxonomic relationship between PF2B19 and other related members of the genus Nesterenkonia. (Halostagnicola larsenii JCM 13463 was used as an outgroup).
Figure 1.
Phylogenetic tree displaying the taxonomic relationship between PF2B19 and other related members of the genus Nesterenkonia. (Halostagnicola larsenii JCM 13463 was used as an outgroup).
Figure 2.
Circular map generated using BRIG program highlighting the differences between PF2B19 and publicly available Nesterenkonia genomes.
Figure 2.
Circular map generated using BRIG program highlighting the differences between PF2B19 and publicly available Nesterenkonia genomes.
Figure 3.
Pathway for degradation of catechol was elucidated using KEGG server.
Table 1.
Differentiating attributes between PF2B19 and publicly available other Nesterenkonia genomes.
Table 1.
Differentiating attributes between PF2B19 and publicly available other Nesterenkonia genomes.
| Attributes | Strains of the Genus Nesterenkonia * | ||||||
|---|---|---|---|---|---|---|---|
| PF2B19 | CD08_7 | AN1 | F | JCM 19054 | NP1 | DSM 19423 | |
| Accession no. | MDSS00000000 | LQBM00000000 | JEMO00000000 | AFRW00000000 | BAXI00000000 | CBLL00000000 | ATXP00000000 |
| Isolation source | Permafrost soil Svalbard, Arctic | Duodenal mucosa of CD patient | Salt Lake, Iran | Antarctic soil | Sea snail Nassarius glans | Feces of AIDS patient | Black liquor treatment system of a cotton pulp mill |
| Growth temp | 15 °C | 37 °C | 21 °C | 32 °C | 28 °C | 37 °C | 42 °C |
| Size | 3.6 Mb | 2.9 Mb | 3.0 Mb | 2.8 Mb | 2.5 Mb | 2.6 Mb | 2.5 Mb |
| Contigs | 135 | 8 | 42 | 138 | 1086 | 175 | 36 |
| G+C (%) | 69.5 | 67.6 | 67.4 | 71.5 | 67.1 | 62.9 | 63.7 |
| No. of RNAs | 55 | 52 | 52 | 50 | 48 | 49 | 51 |
| No. of subsystem | 394 | 379 | 374 | 347 | 292 | 355 | 343 |
| Coding sequences | 3708 | 2531 | 2846 | 2480 | 3901 | 2435 | 2295 |
* Nesterenkonia sp. PF2B19; Nesterenkonia jeotgali CD08_7; Nesterenkonia sp. AN1; Nesterenkonia sp. F; Nesterenkonia sp. JCM 19054; Nesterenkonia massiliensis NP1; Nesterenkonia alba DSM 19423.
Table 2.
Unique genes detected in PF2B19 genome on comparison to available Nesterenkonia genomes.
| Genome Used for Comparison | No. of Unique Genes Detected in PF2B19 on Comparison | Type of Distinct Genes Detected in Relation to Psychrophilic Lifestyle of PF2B19 | Role |
|---|---|---|---|
| Nesterenkonia alba DSM 19423(T) | 323 |
| Counteract against cold-induced osmotic stress |
| Counteract against cold-induced oxidative stress | ||
| Modulate membrane fluidity at low temperatures | ||
| Nesterenkonia massilensis NP1 | 310 |
| Carbon Starvation |
| Counteract against cold-induced osmotic stress | ||
| Counteract against cold-induced oxidative stress | ||
| Nesterenkonia sp. F | 215 |
| Counteract against cold-induced osmotic stress |
| Counteract against cold-induced oxidative stress | ||
| Carbon starvation | ||
| Modulate membrane fluidity at low temperatures | ||
| Nesterenkonia jeotgali CD08_7 | 218 |
| Counteract against cold-induced osmotic stress |
| Counteract against cold-induced oxidative stress | ||
| Carbon starvation | ||
| Nesterenkonia sp. AN1 | 202 |
| Counteract against cold-induced osmotic stress |
| Counteract against cold-induced oxidative stress | ||
| Carbon starvation | ||
| Nesterenkonia sp. JCM 19054 | 345 |
| Cold shock response |
| Counteract against cold-induced osmotic stress | ||
| Counteract against cold-induced oxidative stress | ||
| Carbon starvation |
Table 3.
Cold-induced stress associated genes in Nesterenkonia sp. PF2B19 genome.
| Gene Name | Gene Products | Function |
|---|---|---|
| cshA | Putative ATP-dependent RNA helicase | Cold stress |
| cspC | Cold shock protein C | |
| cspA | Cold shock protein A | |
| infB | Translation initiation factor 1 | |
| deaD | DEAD-box ATP-dependent RNA helicase CshA | |
| Pnp | Polyribonucleotide nucleotidyl transferase | |
| infB | Translation initiation factor 2 | |
| rbfA | Ribosome-binding factor A | |
| nusA | Transcription termination protein | |
| dnaJ | Chaperone protein | |
| dnaK | Chaperone protein | |
| grpE | Heat shock protein | |
| hrpA | ATP-dependent helicase | |
| ygcA | RNA methyltransferase, TrmA family | |
| cstA | Carbon starvation protein A | |
| hrpA | ATP-dependent helicase | |
| recA | Recombinase | DNA repair |
| recN | DNA repair protein | |
| recR | Recombination protein | |
| uvrA | Excinuclease ABC subunit A paralog of unknown function | |
| xthA | Exodeoxyribonuclease III | |
| mutM | Formamidopyrimidine-DNA glycosylase | |
| mutY | A/G-specific adenine glycosylase | |
| recA | RecA protein | |
| recX | Regulatory protein | |
| uvrC | Excinuclease ABC subunit C | |
| uvrB | Excinuclease ABC subunit B | |
| uvrA | Excinuclease ABC subunit A | |
| ruvA | Holliday junction DNA helicase | |
| ruvB | Holliday junction DNA helicase | |
| ruvC | Crossover junction endodeoxyribonuclease | |
| recO | DNA recombination and repair protein | |
| Pdg | Endonuclease III | |
| -- | Phytoene dehydrogenase and related proteins | Membrane fluidity |
| -- | Fatty acid desaturase | |
| hepT | Octaprenyl diphosphate synthase | |
| fabG | 3-oxoacyl-[acyl-carrier protein] reductase | |
| CrtEb | Lycopene elongase | |
| crtB | Phytoene synthase | |
| Idi | Isopentenyl-diphosphate delta-isomerase | |
| fabG | short-chain dehydrogenase/reductase SDR | |
| aas | 1-acyl-sn-glycerol-3-phosphate acyltransferase | |
| Gds | Geranylgeranyl diphosphate synthase | |
| fabH | 3-oxoacyl-[ACP] synthase III in alkane synthesis cluster | |
| fabF | 3-oxoacyl-[acyl-carrier-protein] synthase, KASII | |
| plsC | 1-acyl-sn-glycerol-3-phosphate acyltransferase | |
| pcaH | Protocatechuate 3,4-dioxygenase beta chain | Oxidative stress |
| pcaG | Protocatechuate 3,4-dioxygenase alpha chain | |
| trxC | Thiosulfate sulfurtransferase, rhodanese | |
| ntcA | Transcriptional regulator, Crp/Fnr family | |
| Lactoylglutathione lyase | ||
| yrkH | Hydroxyacylglutathione hydrolase | |
| sodC | Superoxide dismutase [Cu-Zn] precursor | |
| Cob | NAD-dependent protein deacetylase of SIR2 family | |
| --- | Glutathione S-transferase domain protein | |
| hcaC | Ferredoxin, 2Fe-2S | |
| soda | Superoxide dismutase [Mn] | |
| Fur | Zinc uptake regulation protein ZUR | |
| Gap | NADPH-dependent glyceraldehyde-3-phosphate dehydrogenase | |
| kata | Catalase | |
| nrdH | Glutaredoxin-like protein NrdH, required for reduction of Ribonucleotide reductase class Ib | |
| trxA | Thioredoxin | |
| trxB | Thioredoxin reductase | |
| capD | Gamma-glutamyltranspeptidase | |
| -- | Lactoylglutathione lyase and related lyases | |
| msrA | Peptide methionine sulfoxide reductase | |
| Dps | Ferroxidase | |
| yeaX | Vanillate O-demethylase oxidoreductase | |
| Line | Glyoxalase family protein | |
| Ohr | Organic hydroperoxide resistance protein | |
| rsmE | Ribosomal RNA small subunit methyltransferase E | |
| ywrD | Gamma-glutamyltranspeptidase | |
| ahpC | Alkyl hydroperoxide reductase subunit C-like protein | |
| Bcp | Thiol peroxidase, Bcp-type | |
| trxB | Thioredoxin reductase | |
| pncB1 | Nicotinate phosphoribosyltransferase | |
| Fur | Transcriptional regulator, FUR family | |
| hcaC | 3-phenylpropionate dioxygenase ferredoxin subunit | |
| bphG | Ferredoxin reductase | |
| pcaR | Transcriptional regulator, IclR family | |
| cobB1 | NAD-dependent protein deacetylase of SIR2 family | |
| ntcA | Transcriptional regulator, Crp/Fnr family | |
| bphC | Catechol 2,3-dioxygenase | |
| bphG | 3-phenylpropionate dioxygenase ferredoxin subunit | |
| Nicotinamidase | ||
| betA | Choline dehydrogenase | Osmo-protection |
| betP | High-affinity choline uptake protein | |
| gltB | Glutamate synthase [NADPH] large chain | |
| betC | Choline-sulfatase | |
| opuD | Glycine betaine transporter | |
| opuCA | L-proline glycine betaine ABC transport system permease protein ProV | |
| otsB | Trehalose-6-phosphate phosphatase | |
| proW | L-proline glycine betaine ABC transport system permease protein | |
| tcrY | Osmosensitive K+ channel histidine kinase KdpD | |
| otsA | Alpha, alpha-trehalose-phosphate synthase [UDP-forming] | |
| - | Na(+) H(+) antiporter subunit G | |
| - | Na(+) H(+) antiporter subunit F | |
| mrpD | Na(+) H(+) antiporter subunit D | |
| mrpE | Na(+) H(+) antiporter subunit E | |
| mnhC1 | Na(+) H(+) antiporter subunit C | |
| mrpA | Na(+) H(+) antiporter subunit A; Na(+) H(+) antiporter subunit B | |
| opuCB | Glycine betaine ABC transport system permease protein | |
| mrpG | Na(+) H(+) antiporter subunit G | |
| mrpC | Na(+) H(+) antiporter subunit C | |
| - | FIG152265: Sodium:solute symporter associated protein | |
| - | Na(+) H(+) antiporter subunit F | |
| - | Na(+) H(+) antiporter subunit E | |
| mrpD | Na(+) H(+) antiporter subunit D | |
| betT | High-affinity choline uptake protein | |
| gltB | Glutamate synthase [NADPH] small chain | |
| ectA | L-2,4-diaminobutyric acid acetyltransferase | |
| gbsA | Betaine aldehyde dehydrogenase | |
| betA | Choline dehydrogenase | |
| baeS | Osmosensitive K+ channel histidine kinase KdpD | |
| - | Glutamate synthase [NADPH] large chain | |
| gltB | Glutamate synthase [NADPH] small chain | |
| opuBB | Glycine betaine ABC transport system permease protein | |
| putA | Proline dehydrogenase (Proline oxidase) | |
| ectC | L-ectoine synthase | |
| ectB | Diaminobutyrate-pyruvate aminotransferase | |
| panF | Sodium:solute symporter, putative | |
| treS | Trehalose synthase | |
| osmF | L-proline glycine betaine binding ABC transporter protein ProX | |
| - | Universal stress protein | General stress |
| - | Serine phosphatase RsbU, regulator of sigma subunit | |
| glbO | Hemoglobin-like protein HbO | |
| rpoE | RNA polymerase sigma-70 factor, ECF subfamily |
Table 4.
PF2B19 genome-derived cold-adapted enzymes with their biotechnological applications.
| Cold-Active Enzymes Detected in PF2B19 Genome | Applications |
|---|---|
| Lipase, protease, phytase, xylanase | Improves digestibility and assimilation of animal feed |
| Chitinase, Protease | Meat tenderizing |
| α-amylase, xylanase | Textile industry |
| Esterase | Chiral resolution of drugs to escalate effectiveness and range |
| β-lactamase | Antibiotic degradation |
| Lipase | Cosmetics, detergents |
| Chitinase | Additive for anti-fungal creams and lotions, Anti-fungal drug |
| β-galactosidase | Bioethanol production from dairy waste, improves the digestibility of dairy products for lactose-intolerant consumers |
| β-glucosidase | Wine industry |
| Xylanase | Biobleaching in paper and pulp industry |
| Lipase | Biodiesel production by trans-esterification of oils and alcohols |
| Alkaline phosphatase | Cloning experiments in molecular biology |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Singh, P.; Kapse, N.; Gowdaman, V.; Tsuji, M.; Singh, S.M.; Dhakephalkar, P.K. Comparative Genomic Analysis of Arctic Permafrost Bacterium Nesterenkonia sp. PF2B19 to Gain Insights into Its Cold Adaptation Tactic and Diverse Biotechnological Potential. Sustainability 2021, 13, 4590. https://0-doi-org.brum.beds.ac.uk/10.3390/su13084590
AMA Style
Singh P, Kapse N, Gowdaman V, Tsuji M, Singh SM, Dhakephalkar PK. Comparative Genomic Analysis of Arctic Permafrost Bacterium Nesterenkonia sp. PF2B19 to Gain Insights into Its Cold Adaptation Tactic and Diverse Biotechnological Potential. Sustainability. 2021; 13(8):4590. https://0-doi-org.brum.beds.ac.uk/10.3390/su13084590
Chicago/Turabian StyleSingh, Purnima, Neelam Kapse, Vasudevan Gowdaman, Masaharu Tsuji, Shiv Mohan Singh, and Prashant K. Dhakephalkar. 2021. "Comparative Genomic Analysis of Arctic Permafrost Bacterium Nesterenkonia sp. PF2B19 to Gain Insights into Its Cold Adaptation Tactic and Diverse Biotechnological Potential" Sustainability 13, no. 8: 4590. https://0-doi-org.brum.beds.ac.uk/10.3390/su13084590
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
