Search tips
Search criteria 


Logo of genannJournal InfoAuthorsPermissionsJournals.ASM.orggenomeA ArticleGenome Announcements
Genome Announc. 2017 September; 5(38): e00710-17.
Published online 2017 September 21. doi:  10.1128/genomeA.00710-17
PMCID: PMC5609402

Draft Genome Sequence of Natronolimnobius baerhuensis CGMCC 1.3597T, an Aerobic Haloalkaliphilic Archaeon Isolated from a Soda Lake


The haloalkaliphilic archaeon Natronolimnobius baerhuensis was isolated from a soda lake in Inner Mongolia (China), growing optimally at about 20% NaCl and pH 9.0. The draft genome consists of approximately 3.91 Mb and contains 3,810 predicted genes. Some genes that regulate intracellular osmotic stress and pH homeostasis were identified, providing insight into specific adaptations to this double-extreme environment.


The mesophilic haloalkaliphile Natronolimnobius baerhuensis (strain CGMCC 1.3597T = JCM 12253T) is a strictly aerobic Gram-negative archaeon isolated from soda lakes in Inner Mongolia, China (1). This strain is the type species of the genus Natronolimnobius, which thus far contains only two haloalkaliphiles. N. baerhuensis is an extremely halophilic alkaliphile because it requires at least 15% NaCl (optimum, 20% NaCl) and grows at pH 7.0 to 10.0 (optimum, pH 9.0). To gain insight into the survival and adaptation strategies under double-extreme environmental stress, the draft whole genome of N. baerhuensis strain CGMCC 1.3597T was sequenced.

Genomic DNA was extracted using a microbial DNA isolation kit according to the manufacturer’s instructions (New Industry, Beijing, China). Library construction for genome sequencing was prepared using the NEBNext Ultra DNA library prep kit of Illumina (2). Sequencing was performed by the Illumina HiSeq 4000 sequencer with a paired-end read length of 2 × 150 bp at approximately 200× coverage. Genomic contigs were de novo assembled using MicrobeTrakr plus version 0.9.1 (incorporates Velvet version 1.2.09). Quake (3) and BWA (4) were used in preassembly and postassembly sequence correction, respectively. A total of 5,752,927 reads were assembled into eight contigs, with a total length of 3,914,301 bp, G+C content of 59.2%, and N50 value of 1,261,254 bp. The assembled genome was annotated using NCBI Prokaryotic Genome Annotation Pipeline ( (5) and checked by the GenBank curation team. Among the 3,810 genes predicted, 3,662 were potential protein-coding genes (CDSs). Also identified were 45 RNAs, including 8 rRNAs (six 5S RNAs, one 16S RNA, and one 23S RNA), 45 tRNAs, and two noncoding RNAs (ncRNAs).

Genome sequence analysis revealed various genes that code for proteins potentially related to the adaptation of N. baerhuensis to highly saline and alkaline environments. Two genes encode trehalose-6-phosphate synthase (TPS) and trehalose-6-phosphate phosphatase (TPP) for trehalose biosynthesis, and two genes encode sodium-solute symporter (SSS). These genes implied that N. baerhuensis is involved in the maintenance of osmotic balance via the compatible-solutes strategy under hypersaline conditions (6, 7). The analysis identified 10 genes (eight TrkA-type and two TrkH-type) that are responsible for K+ uptake systems, which indicates that N. baerhuensis also achieves an isosmotic cytoplasm using K+ as an osmolyte via the salt-in strategy (6, 7). N. baerhuensis is an obligate halophilic alkaliphile and therefore must have mechanisms for cytoplasmic acidification because it has 4 genes of the multisubunit Na+/H+ antiporter (CPA-3 family), 4 genes of the monovalent cation/H+ antiporters (CPA-1 family), and 1 gene of the Na+/H+ antiporter (NhaC type). Furthermore, five genes were identified from the Kef-type K+ efflux system, which protects cells against the detrimental effects of electrophilic compounds via cytoplasmic acidification. In this report, the predicted genes play essential roles in maintaining stable osmotic balance and pH homeostasis to avoid cell intoxication.

Accession number(s).

The draft genome assembly of N. baerhuensis CGMCC 1.3597T has been deposited at DDBJ/ENA/GenBank under the accession number MWPH00000000.


This work was supported by grants 31570110 and 31370158 from the National Science Foundation of China (NSFC) and grants 0042014011 and 1610042017001 from the Foundation of Graduate School of Chinese Academy of Agricultural Sciences (CAAS).


Citation Guo X, Liao Z, Yan Y, Holtzapple M, Hu Q, Zhao B. 2017. Draft genome sequence of Natronolimnobius baerhuensis CGMCC 1.3597T, an aerobic haloalkaliphilic archaeon isolated from a soda lake. Genome Announc 5:e00710-17.


1. Itoh T, Yamaguchi T, Zhou P, Takashina T 2005. Natronolimnobius baerhuensis gen. nov., sp. nov. and Natronolimnobius innermongolicus sp. nov., novel haloalkaliphilic archaea isolated from soda lakes in Inner Mongolia, China. Extremophiles 9:111–116. doi:.10.1007/s00792-004-0426-z [PubMed] [Cross Ref]
2. Famewo EB, Clarke AM, Afolayan AJ 2016. Identification of bacterial contaminants in polyherbal medicines used for the treatment of tuberculosis in Amatole District of the Eastern Cape Province, South Africa, using rapid 16S rRNA technique. J Health Popul Nutr 35:27. doi:.10.1186/s41043-016-0064-y [PMC free article] [PubMed] [Cross Ref]
3. Kelley DR, Schatz MC, Salzberg SL 2010. Quake: quality-aware detection and correction of sequencing errors. Genome Biol 11:R116. doi:.10.1186/gb-2010-11-11-r116 [PMC free article] [PubMed] [Cross Ref]
4. Li H. 2013. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv arXiv:1303.3997
5. Shen Z, Mannion A, Whary MT, Muthupalani S, Sheh A, Feng Y, Gong G, Vandamme P, Holcombe HR, Paster BJ, Fox JG 2016. Helicobacter saguini, a novel helicobacter isolated from cotton-top tamarins with ulcerative colitis, has proinflammatory properties and induces typhlocolitis and dysplasia in gnotobiotic IL-10−/− mice. Infect Immun 84:2307–2316. doi:.10.1128/IAI.00235-16 [PMC free article] [PubMed] [Cross Ref]
6. Banciu HL, Muntyan MS 2015. Adaptive strategies in the double-extremophilic prokaryotes inhabiting soda lakes. Curr Opin Microbiol 25:73–79. doi:.10.1016/j.mib.2015.05.003 [PubMed] [Cross Ref]
7. Banciu HL, Sorokin DY 2013. Adaptation in haloalkaliphiles and natronophilic bacteria, p 121–178. In Seckbach J, Oren A, Stan-Lotter H (), Polyextremophiles: life under multiple forms of stress. Springer, Dordrecht, The Netherlands.

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)