ABSTRACT
Methylomonas denitrificans strain FJG1 is a member of the gammaproteobacterial methanotrophs. The sequenced genome of FJG1 reveals the presence of genes that encode methane, methanol, formaldehyde, and formate oxidation. It also contains genes that encode enzymes for nitrate reduction to nitrous oxide, consistent with the ability of FJG1 to couple denitrification with methane oxidation.
GENOME ANNOUNCEMENT
The genus Methylomonas belongs to the class Gammaproteobacteria, order Methylococcales, and family Methylococcaceae (1). Members of this genus are able to utilize methane as their sole source of carbon and energy (2). Methane is a common low-value industrial by-product (3) and is a more potent greenhouse gas than carbon dioxide (4). Methanotrophs play a key role in the global carbon cycle (5) and can be used to convert methane into value-added products such as biofuels and biopolymers (3). Here, we report the complete genome sequence of Methylomonas denitrificans strain FJG1, a recently described methanotrophic species (6).
Genomic DNA from M. denitrificans strain FJG1 was extracted using the MasterPure complete DNA and RNA purification kit (Epicentre). Sequencing libraries were then prepared using the RS II SMRTbell template preparation kit 1.0 (Pacific Biosciences) and sequenced with the P6 v2 single-molecule real-time (SMRT) sequencing platform (Pacific Biosciences). The 300,584 raw reads resulted in 106,388 quality-filtered trimmed reads, which were subsequently assembled de novo using the Hierarchical Genome Assembly Process of the SMRT Analysis software 2.2 (7). The resulting genome is 5,172,098 bp in size, with a G+C content of 51.7% and a coverage of 228×. Whole-genome comparisons (8, 9) of FJG1 with other Methylomonas strains reveal its highest similarity with Methylomonas methanica NCIMB 11130 (10).
The genome of FJG1 was annotated using the Prokaryotic Genome Annotation Pipeline 4.1 (11) to reveal 4,559 protein-coding genes, 3 rRNA operons (16S, 23S, and 5S), 47 tRNAs, and 4 noncoding RNAs (ncRNAs). The aerobic oxidation of methane to methanol is catalyzed by methane monooxygenase (2). Strain FJG1 contains the operons pmoCAB and pxmABC, which encode particulate methane monooxygenase (pMMO) and copper-containing membrane monooxygenase (12). However, the soluble methane monooxygenase operon (mmoXYBZDCGR) (13) is not present. The genome also contains genes encoding cyanoglobins (hbN), one of which is upregulated under hypoxic conditions and hypothesized to bind oxygen for delivery to pMMO (6). Methanol is converted to formaldehyde by pyrroloquinoline quinone (PQQ)-dependent methanol dehydrogenases (2). Gene clusters for methanol dehydrogenases (mxaDFJGIRSACKL and xoxFJ) and PQQ biosynthesis (pqqABCDE and pqqFG) are present. Also present are genes involved in formaldehyde oxidation, including those for the tetrahydromethanopterin (fae, fhcCDAB, mch, mptG, and mtdB) and tetrahydrofolate (fch, fhs, and mtdA) pathways and an NAD-dependent formate dehydrogenase (fdsABGCD) for formate oxidation. Additionally, genes involved in C1 assimilation through the ribulose monophosphate, tricarboxylic acid, Embden-Meyerhof-Parnas, and Entner-Doudoroff pathways were identified.
FJG1 possesses genes for nitrogen acquisition, including ammonium (amtB), nitrate (narK and nrtA), and urea (urtABCDE) transporters, and urease genes (ureABCDEFG). Genes for denitrification, namely, nitrate (narGHJI and napABC), nitrite (nirK and nirS), and nitric oxide (norCB) reductases, are also present. The strain contains alanine dehydrogenase (aldA) for the assimilation of ammonium by reductive amination of pyruvate (2). Assimilatory nitrate (nasA) and nitrite (nirBD) reductases are also present. In contrast, under ammonium-limiting conditions, ammonia is assimilated through the glutamine synthetase (glnA)-glutamate synthase (gltB) pathway (2), both of which are also present in FJG1.
Accession number(s).
The whole-genome sequence of M. denitrificans FJG1 has been deposited in GenBank under the accession number CP014476. The version described in this paper is the first version, CP014476.1.
ACKNOWLEDGMENTS
F.D.O. was supported by funding from the Future Energy Systems Research Initiative of the University of Alberta, K.D.K. was supported by a fellowship from Alberta Innovates–Technology Futures, and L.Y.S. was supported by a Natural Sciences and Engineering Research Council Discovery Grant.
Footnotes
Citation Orata FD, Kits KD, Stein LY. 2018. Complete genome sequence of Methylomonas denitrificans strain FJG1, an obligate aerobic methanotroph that can couple methane oxidation with denitrification. Genome Announc 6:e00276-18. https://doi.org/10.1128/genomeA.00276-18.
REFERENCES
- 1.Bowman JP. 2005. Genus V. Methylomonas, p 265–268. In Brenner DJ, Krieg NR, Staley JT, Garrity GM, Boone DR, De Vos P, Goodfellow M, Rainey FA, Schleifer KH (ed), Bergey’s manual of systematic bacteriology , 2nd ed, vol 2 Springer, New York, NY. [Google Scholar]
- 2.Trotsenko YA, Murrell JC. 2008. Metabolic aspects of aerobic obligate methanotrophy. Adv Appl Microbiol 63:183–229. doi: 10.1016/S0065-2164(07)00005-6. [DOI] [PubMed] [Google Scholar]
- 3.Strong PJ, Xie S, Clarke WP. 2015. Methane as a resource: can the methanotrophs add value? Environ Sci Technol 49:4001–4018. doi: 10.1021/es504242n. [DOI] [PubMed] [Google Scholar]
- 4.Yvon-Durocher G, Allen AP, Bastviken D, Conrad R, Gudasz C, St-Pierre A, Thanh-Duc N, del Giorgio PA. 2014. Methane fluxes show consistent temperature dependence across microbial to ecosystem scales. Nature 507:488–491. doi: 10.1038/nature13164. [DOI] [PubMed] [Google Scholar]
- 5.Cicerone RJ, Oremland RS. 1988. Biogeochemical aspects of atmospheric methane. Global Biogeochem Cycles 2:299–327. doi: 10.1029/GB002i004p00299. [DOI] [Google Scholar]
- 6.Kits KD, Klotz MG, Stein LY. 2015. Methane oxidation coupled to nitrate reduction under hypoxia by the gammaproteobacterium Methylomonas denitrificans, sp. nov. type strain FJG1. Environ Microbiol 17:3219–3232. doi: 10.1111/1462-2920.12772. [DOI] [PubMed] [Google Scholar]
- 7.Chin CS, Alexander DH, Marks P, Klammer AA, Drake J, Heiner C, Clum A, Copeland A, Huddleston J, Eichler EE, Turner SW, Korlach J. 2013. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data. Nat Methods 10:563–569. doi: 10.1038/nmeth.2474. [DOI] [PubMed] [Google Scholar]
- 8.Richter M, Rosselló-Móra R. 2009. Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci U S A 106:19126–19131. doi: 10.1073/pnas.0906412106. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Meier-Kolthoff JP, Auch AF, Klenk HP, Göker M. 2013. Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 14:60. doi: 10.1186/1471-2105-14-60. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Heylen K, De Vos P, Vekeman B. 2016. Draft genome sequences of eight obligate methane oxidizers occupying distinct niches based on their nitrogen metabolism. Genome Announc 4:e00421-16. doi: 10.1128/genomeA.00421-16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Tatusova T, DiCuccio M, Badretdin A, Chetvernin V, Nawrocki EP, Zaslavsky L, Lomsadze A, Pruitt KD, Borodovsky M, Ostell J. 2016. NCBI Prokaryotic Genome Annotation Pipeline. Nucleic Acids Res 44:6614–6624. doi: 10.1093/nar/gkw569. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Tavormina PL, Orphan VJ, Kalyuzhnaya MG, Jetten MS, Klotz MG. 2011. A novel family of functional operons encoding methane/ammonia monooxygenase-related proteins in gammaproteobacterial methanotrophs. Environ Microbiol Rep 3:91–100. doi: 10.1111/j.1758-2229.2010.00192.x. [DOI] [PubMed] [Google Scholar]
- 13.Nguyen NL, Yu WJ, Yang HY, Kim JG, Jung MY, Park SJ, Roh SW, Rhee SK. 2017. A novel methanotroph in the genus Methylomonas that contains a distinct clade of soluble methane monooxygenase. J Microbiol 55:775–782. doi: 10.1007/s12275-017-7317-3. [DOI] [PubMed] [Google Scholar]