Jordan Krebs Tom Sontag, Jeffrey Newman Lycoming College
Genome Sequencing of Lycomia zaccaria gen.
- nov. sp. nov., Chryseobacterium haifense, and
Genome Sequencing of Lycomia zaccaria gen. nov. sp. nov. , - - PowerPoint PPT Presentation
Genome Sequencing of Lycomia zaccaria gen. nov. sp. nov. , Chryseobacterium haifense , and Kaistella koreensis and Comparison to Two Closely Related Genomes Jordan Krebs Tom Sontag, Jeffrey Newman Lycoming College Species Introduction
Chryseobacterium shigense Chryseobacterium vrystaatense Chryseobacterium luteum Chryseobacterium sp. KM Chryseobacterium joostei Chryseobacterium jejuense Chryseobacterium oranimense Chryseobacterium gleum Chryseobacterium soli Chryseobacterium soldanellicola Chryseobacterium sp. CTM Chryseobacterium sp. VR86 Chryseobacterium greenlandense Kaistella koreensis Chryseobacterium haifense Lycomia zaccaria JJC 3519
0.005
Phylogenetic and molecular evolutionary analyses were conducted using MEGA version 5 (Tamura, Peterson, Stecher, Nei, and Kumar 2011).
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Function‐Based Analysis Sequence‐Based Analysis Download Reference Genomes Sequence Genomes Assemble
3519 L. zaccaria JJC C. haifense Find and Annotate Genes Upload into RAST K. koreensis
Amino Acids and Derivatives Fatty Acids, Lipids, and Isoprenoids Carbohydrates Membrane Transport Protein Metabolism Metabolism of Aromatic Compounds DNA Metabolism Cell Division and Cell Cycle RNA metabolism Nitrogen Metabolism Cell Wall and Capsule Phosphorus Metabolism Cofactors, Vitamins, Prosthetic Groups, Pigments Regulation and Cell Signaling Virulence, Disease, and Defense Potassium Metabolism Nucleosides and Nucelotides Sulfur Metabolism Stress Response Dormancy and Sporulation Miscellaneous Iron Acquistion and Metabolism Secondary Metabolism Phages, Prophages, Transposable elements, Plasmids Subsystems Respiration
81 43 89 20 64 73 25 9 86 140 74 115 81 40 118
12 20
3.2 Mbp
5.6 Mbp
3.8 Mbp
3.5 Mbp 3519 2.8 Mbp
Figure inspired by Figure of http://xsplat.wordpress.com
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Beta‐lactamase Gliding motility Ornithine , Xaa‐Pro Aminopeptidases DEAD‐box protein A Mn superoxide dismutase GroEL, GroES, GrpE Catalase
Molybdenum cofactors biosynthesis Trehalose permease (FucP) Trehalase Sulfite reductase Siderophore synthesis Flexirubin synthesis (darA) Alanine racemase Phage tail fiber protein Retron‐type RNA‐ directed DNA polymerase Integron integrase Minor curlin subunit CsgB (nucleation) Serine phospatase RsbU – regulator of sigma subunit Sucrose‐6‐phosphate hydrolase Alpha‐acetolactate decarboxylase Bacterophytochrome heme
Catechol 1,2‐dioxygenase D‐beta‐hydroxybutyrate dehydrogenase Methylglyoxal synthase
Formate‐THF ligase P yruvate, phosphate‐ dikinase Beta‐lactamase/Penicillin binding proteins Cytosine deaminase Arginino‐ succinate Syn. Fumarate hydratase Butyryl‐CoA dehydro‐ genase Serine acetyl‐ trans‐ ferase Thiol peroxi‐ dase, Tpx‐type Amino‐ deoxych‐
lyase methyleneTHF reductase Cystathionine
Amino Acids and Derivatives Carbohydrates Protein Metabolism DNA Metabolism RNA metabolism Cell Wall and Capsule Cofactors, Vitamins, Prosthetic Groups, Pigments Virulence, Disease, and Defense Nucleosides and Nucelotides Stress Response Miscellaneous Respiration Fatty Acids, Lipids, and Isoprenoids Membrane Transport Metabolism of Aromatic Compounds Cell Division and Cell Cycle Nitrogen Metabolism Phosphorus Metabolism Regulation and Cell Signaling Potassium Metabolism Sulfur Metabolism Dormancy and Sporulation Iron Acquistion and Metabolism Secondary Metabolism Phages, Prophages, Transposable elements, Plasmids Subsystems
Adapted from Zhaxybayeva O et al. PNAS 2009;106:5865‐5870
Olsen, G.J., Olson, R., Osterman, A.L., Overbeek, R.A., McNeil, L.K., Paarmann, D., Paczian, T., Parrello, B., Pusch, G.D., Reich, C., Stevens, R., Vassieva, O., Vonstein, V., Wilke, A., & Zagnitko O. (2008). The RAST Server: Rapid Annotations using Subsystems
Description of Chryseobacterium anthropi sp. nov. to accommodate clinical isolates biochemically similar to Kaistella koreensis and Chryseobacterium haifense, proposal to reclassify Kaistella koreensis as Chryseobacterium koreense comb. nov. and emended description of the genus Chryseobacterium. Int J Syst Evol Microbiol 59, 2421–2428.
Analysis using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Molecular Biology and Evolution (submitted).
flavobacteria: description of Chryseobacterium gen. nov., Bergeyella gen. nov., and Empedobacter nom. rev. Int J Syst Bacteriol 44, 827–831.
Gogarten, J.P., and Noll, K.M. (2009). On the chimeric nature, thermophilic origin, and phylogenetic placement of the
From left to right: Back: Dr. Newman, Andrew Gale (‘15), Dillon Snyder (‘14), Tom Sontag (‘14), Logan Mariano (‘13), Me, Clark Thompson (‘13) Front: Jessica Hoffman (‘15), and Jessica Lehman (‘13)