Abstract
The draft genome of Kallotenue papyrolyticum JKG1T, a member of the order Kallotenuales, class Chloroflexia, consists of 4,475,263 bp in 4 contigs and encodes 4,010 predicted genes, 49 tRNA-encoding genes, and 3 rRNA operons. The genome is consistent with a heterotrophic lifestyle including catabolism of polysaccharides and amino acids.
GENOME ANNOUNCEMENT
Strain JKG1T was isolated from a cellulolytic enrichment in Great Boiling Spring, Nevada (1), using optical tweezers and a microfluidic device due to its capacity to grow aerobically on filter paper (optimum 55 °C) (2). Strain JKG1T was described as a member of a new genus and species, Kallotenue papyrolyticum, and a new order, Kallotenuales, of the phylum Chloroflexi (2). It has broad heterotrophic activity, including the capacity to hydrolyze polysaccharides such as carboxymethylcellulose, microcrystalline cellulose, filter paper, xylan, and starch, and proteinaceous substrates such as casamino acids, tryptone, and peptone. K. papyrolyticum is one of several, new high-level taxonomic groups of thermophilic Chloroflexi isolated from Great Boiling spring (3).
The draft genome of strain JKG1T was generated at the DOE Joint genome Institute (JGI) using Pacific Biosciences (PacBio) technology. A PacBio SMRTbell library was constructed and sequenced on the PacBio RS platform, which generated 304,235 filtered subreads totaling 854.0 Mbp. All general aspects of library construction and sequencing performed at the JGI can be found at http://www.jgi.doe.gov. The raw reads were assembled using HGAP (version 2.0.0) (4). The genome was annotated using Prodigal version 2.5 (5), as part of the JGI microbial annotation pipeline (6). The K. papyrolyticum draft genome is 4,475,263 bp in 4 contigs, encoding 4,010 predicted genes, including 49 tRNA-encoding genes, and three rRNA operons. The genome encodes enzymes for complete glycolysis, tricarboxylic acid cycle, and pentose phosphate pathways and dedicates a large amount of its genome to carbohydrate (10.1%; clusters of orthologous groups [COG] category G) and amino acid (8.9%; COG category E) metabolism. Analysis of the genome for carbohydrate-active enzymes (CAZymes) (7) revealed 171 total CAZymes, 55 of which are glycoside hydrolases (GHs), including GHs putatively involved in chitin (GH18), woody plant (GH53), and cellulose (GH5,6,9,10,51) depolymerization. This number of CAZymes and GH domains is similar to other cellulolytic thermophiles, such as Thermotoga maritima (8), Caldicellulosiruptor species (9), and Dictyoglomus turgidum (10).
Catabolism of organic compounds can be coupled to aerobic respiration. Similar to Chloroflexus (11), strain JKG1T has a prototypical respiratory complex I and II to transfer electrons into the quinone pool; however, quinols are likely oxidized by an alternative complex III (ACIII) (12) rather than a bc1/b6f complex The presence of lactate and ethanol dehydrogenases, acetate-CoA ligase, and an iron-only hydrogenase suggest capacity for fermentation, however, fermentation of glucose, casamino acids, or yeast extract was not observed in JKG1T cultures (2). Strain JKG1T may be able to oxidize carbon monoxide through a putative type II carbon monoxide dehydrogenase (CODH) encoded by a cox gene cluster, although the functions of type II CODH are not firmly established (13). Known pathways for phototrophy, autotrophy, and anaerobic respiration are absent, although putative molybdopterin oxidoreductases and multicopper oxidases may be involved in anaerobic respiration.
PFAM domains representing proteins involved in outer membrane biogenesis and transport are not present, suggesting JKG1T has a monoderm cell envelope structure similar to other Chloroflexi (14).
Nucleotide sequence accession numbers.
This whole-genome shotgun project has been deposited in GenBank under accession numbers JAGA01000001 to JAGA01000004.
ACKNOWLEDGMENTS
The work conducted by the U.S. Department of Energy Joint Genome Institute was supported by the Office of Science of the U.S. Department of Energy under contract DE-AC02-05CH11231. Additional support was supported by NSF grant OISE-0968421 to B.P.H. who is also grateful for support from Greg Fullmer through the UNLV Foundation.
Footnotes
Citation Hedlund BP, Murugapiran SK, Huntemann M, Clum A, Pillay M, Palaniappan K, Varghese N, Mikhailova N, Stamatis D, Reddy TBK, Ngan CY, Daum C, Duffy K, Shapiro N, Markowitz V, Ivanova N, Kyrpides N, Williams AJ, Cole JK, Dodsworth JA, Woyke T. 2015. High-quality draft genome sequence of Kallotenue papyrolyticum JKG1T reveals broad heterotrophic capacity focused on carbohydrate and amino acid metabolism. Genome Announc 3(6):e01410-15. doi:10.1128/genomeA.01410-15.
REFERENCES
- 1.Peacock JP, Cole JK, Murugapiran SK, Dodsworth JA, Fisher JC, Moser DP, Hedlund BP. 2013. Pyrosequencing reveals high-temperature cellulolytic microbial consortia in great boiling spring after in situ lignocellulose enrichment. PloS One 8:e59927. doi: 10.1371/journal.pone.0059927. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Cole JK, Gieler BA, Heisler DL, Palisoc MM, Williams AJ, Dohnalkova AC, Ming H, Yu TT, Dodsworth JA, Li W-J, Hedlund BP. 2013. Kallotenue papyrolyticum gen. nov., sp. nov., a cellulolytic and filamentous thermophile that represents a novel lineage (Kallotenuales ord. nov., Kallotenuaceae fam. nov.) within the class Chloroflexia. Int J Syst Evol Microbiol 63:4675–4682. doi: 10.1099/ijs.0.053348-0. [DOI] [PubMed] [Google Scholar]
- 3.Dodsworth JA, Gevorkian J, Despujos F, Cole JK, Murugapiran SK, Ming H, Li W-, Zhang G, Dohnalkova A, Hedlund BP. 2014. Thermoflexus hugenholtzii gen. nov., sp. nov., a thermophilic, microaerophilic, filamentous bacterium representing a novel class in the Chloroflexi, Thermoflexia classis nov, and description of Thermoflexaceae fam. nov. and Thermoflexales ord. nov. Int J Syst Evol Microbiol 64:2119–2127. doi: 10.1099/ijs.0.055855-0. [DOI] [PubMed] [Google Scholar]
- 4.Chin C, 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]
- 5.Hyatt D, Chen G, LoCascio PF, Land ML, Larimer FW, Hauser LJ. 2010. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 11:119. doi: 10.1186/1471-2105-11-119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Huntemann M, Ivanova NN, Mavromatis K, Tripp HJ, Paez-Espino D, Palaniappan K, Szeto E, Pillay M, Chen IM-A, Pati A, Nielsen T, Markowitz VM, Kyrpides NC. 2015. The standard operating procedure of the DOE-JGI microbial genome annotation pipeline (MGAP v.4). Stand Genomic Sci, in press. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Nelson KE, Clayton RA, Gill SR, Gwinn ML, Dodson RJ, Haft DH, Hickey EK, Peterson JD, Nelson WC, Ketchum KA, McDonald L, Utterback TR, Malek JA, Linher KD, Garrett MM, Stewart AM, Cotton MD, Pratt MS, Phillips CA, Richardson D, Heidelberg J, Sutton GG, Fleischmann RD, Eisen JA, White O, Salzberg SL, Smith HO, Venter JC, Fraser CM. 1999. Evidence for lateral gene transfer between Archaea and bacteria from genome sequence of Thermotoga maritima. Nature 399:323–329. doi: 10.1038/20601. [DOI] [PubMed] [Google Scholar]
- 8.Blumer-Schuette SE, Ozdemir I, Mistry D, Lucas S, Lapidus A, Cheng J-, Goodwin LA, Pitluck S, Land ML, Hauser LJ, Woyke T, Mikhailova N, Pati A, Kyrpides NC, Ivanova N, Detter JC, Walston-Davenport K, Han S, Adams MWW, Kelly RM. 2011. Complete genome sequences for the anaerobic, extremely thermophilic plant biomass-degrading bacteria Caldicellulosiruptor hydrothermalis, Caldicellulosiruptor kristjanssonii, Caldicellulosiruptor kronotskyensis, Caldicellulosiruptor owensensis, and Caldicellulosiruptor lactoaceticus. J Bacteriol 193:1483–1484. doi: 10.1128/JB.01515-10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Brumm P, Hermanson S, Hochstein B, Boyum J, Hermersmann N, Gowda K, Mead D. 2011. Mining Dictyoglomus turgidum for enzymatically active carbohydrases. Appl Biochem Biotechnol 163:205–214. doi: 10.1007/s12010-010-9029-6. [DOI] [PubMed] [Google Scholar]
- 10.Cantarel BL, Coutinho PM, Rancurel C, Bernard T, Lombard V, Henrissat B. 2009. The carbohydrate-active EnZymes database (CAZy): an expert resource for glycogenomics. Nucleic Acids Res 37:D233–D238. doi: 10.1093/nar/gkn663. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Yanyushin MF, del Rosario MC, Brune DC, Blankenship RE. 2005. New class of bacterial membrane oxidoreductases. Biochemistry 44:10037–10045. doi: 10.1021/bi047267l. [DOI] [PubMed] [Google Scholar]
- 12.Refojo PN, Teixeira M, Pereira MM. 2012. The alternative complex III: Properties and possible mechanisms for electron transfer and energy conservation. Biochim Biophys Acta 1817:1852–1859. doi: 10.1016/j.bbabio.2012.05.003. [DOI] [PubMed] [Google Scholar]
- 13.King GM, Weber CF. 2007. Distribution, diversity and ecology of aerobic CO-oxidizing bacteria. Nat Rev Microbiol 5:107–118. doi: 10.1038/nrmicro1595. [DOI] [PubMed] [Google Scholar]
- 14.Sutcliffe IC. 2011. Cell envelope architecture in the Chloroflexi: a shifting frontline in a phylogenetic turf war. Environ Microbiol 13:279–282. doi: 10.1111/j.1462-2920.2010.02339.x. [DOI] [PubMed] [Google Scholar]