Flexilinea flocculi JCM 30897 is an obligate anaerobe, chemoorganotroph, Gram-negative bacterium that was isolated from A methanogenic granular sludge in a full-scale mesophilic UASB reactor treating high-strength starch-based organic wastewater.
Gram-negative filament-shaped obligate anaerobe chemoorganotroph 16S sequence Bacteria| @ref 20215 |
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| Domain Bacteria |
| Phylum Chloroflexota |
| Class Anaerolineae |
| Order [Anaerolineae, not assigned to order] |
| Family [Anaerolineae, not assigned to family] |
| Genus Flexilinea |
| Species Flexilinea flocculi |
| Full scientific name Flexilinea flocculi Sun et al. 2016 |
| @ref | Gram stain | Cell length | Cell width | Cell shape | Motility | |
|---|---|---|---|---|---|---|
| 43788 | negative | 100 µm | 0.3-0.4 µm | filament-shaped |
| 43788 | Oxygen toleranceobligate anaerobe |
| 43788 | Typechemoorganotroph |
| @ref | Chebi-ID | Metabolite | Utilization activity | Kind of utilization tested | |
|---|---|---|---|---|---|
| 43788 | 30089 ChEBI | acetate | - | assimilation | |
| 43788 | 22599 ChEBI | arabinose | + | growth | |
| 43788 | 16150 ChEBI | benzoate | - | assimilation | |
| 43788 | 17750 ChEBI | betaine | - | assimilation | |
| 43788 | 17750 ChEBI | betaine | - | growth | |
| 43788 | 17968 ChEBI | butyrate | - | assimilation | |
| 43788 | casamino acids | - | assimilation | ||
| 43788 | 35899 ChEBI | crotonate | - | assimilation | |
| 43788 | 18276 ChEBI | dihydrogen | - | assimilation | |
| 43788 | 33403 ChEBI | elemental sulfur | - | electron acceptor | |
| 43788 | 16236 ChEBI | ethanol | - | assimilation | |
| 43788 | 29034 ChEBI | ferric iron | - | electron acceptor | |
| 43788 | 28757 ChEBI | fructose | + | growth | |
| 43788 | 29806 ChEBI | fumarate | - | assimilation | |
| 43788 | 29806 ChEBI | fumarate | - | electron acceptor | |
| 43788 | 28260 ChEBI | galactose | - | growth | |
| 43788 | 17234 ChEBI | glucose | + | growth | |
| 43788 | 15978 ChEBI | glycerol 3-phosphate | - | assimilation | |
| 43788 | 24996 ChEBI | lactate | - | assimilation | |
| 43788 | 25115 ChEBI | malate | - | assimilation | |
| 43788 | 37684 ChEBI | mannose | - | growth | |
| 43788 | 17790 ChEBI | methanol | - | assimilation | |
| 43788 | 17632 ChEBI | nitrate | - | electron acceptor | |
| 43788 | 17309 ChEBI | pectin | - | growth | |
| 43788 | peptone | - | assimilation | ||
| 43788 | 46793 ChEBI | polyethylene glycol | - | assimilation | |
| 43788 | 28831 ChEBI | propanol | - | assimilation | |
| 43788 | 17272 ChEBI | propionate | - | assimilation | |
| 43788 | 15361 ChEBI | pyruvate | + | growth | |
| 43788 | 16634 ChEBI | raffinose | - | assimilation | |
| 43788 | 33942 ChEBI | ribose | + | growth | |
| 43788 | 28017 ChEBI | starch | + | growth | |
| 43788 | 30031 ChEBI | succinate | - | assimilation | |
| 43788 | 17992 ChEBI | sucrose | - | assimilation | |
| 43788 | 16189 ChEBI | sulfate | - | electron acceptor | |
| 43788 | 17359 ChEBI | sulfite | - | electron acceptor | |
| 43788 | 16094 ChEBI | thiosulfate | - | electron acceptor | |
| 43788 | tryptone | - | growth | ||
| 43788 | 37166 ChEBI | xylan | - | assimilation | |
| 43788 | 18222 ChEBI | xylose | + | growth | |
| 43788 | yeast extract | + | required for growth |
| @ref | pathway | enzyme coverage | annotated reactions | external links | |
|---|---|---|---|---|---|
| 66794 | gluconeogenesis | 100 | 8 of 8 | ||
| 66794 | vitamin E metabolism | 100 | 4 of 4 | ||
| 66794 | kanosamine biosynthesis II | 100 | 2 of 2 | ||
| 66794 | metabolism of amino sugars and derivatives | 100 | 5 of 5 | ||
| 66794 | acetoin degradation | 100 | 3 of 3 | ||
| 66794 | coenzyme A metabolism | 100 | 4 of 4 | ||
| 66794 | CDP-diacylglycerol biosynthesis | 100 | 2 of 2 | ||
| 66794 | UDP-GlcNAc biosynthesis | 100 | 3 of 3 | ||
| 66794 | folate polyglutamylation | 100 | 1 of 1 | ||
| 66794 | suberin monomers biosynthesis | 100 | 2 of 2 | ||
| 66794 | ceramide biosynthesis | 100 | 1 of 1 | ||
| 66794 | anapleurotic synthesis of oxalacetate | 100 | 1 of 1 | ||
| 66794 | L-lactaldehyde degradation | 100 | 3 of 3 | ||
| 66794 | serine metabolism | 88.89 | 8 of 9 | ||
| 66794 | chorismate metabolism | 88.89 | 8 of 9 | ||
| 66794 | valine metabolism | 88.89 | 8 of 9 | ||
| 66794 | C4 and CAM-carbon fixation | 87.5 | 7 of 8 | ||
| 66794 | reductive acetyl coenzyme A pathway | 85.71 | 6 of 7 | ||
| 66794 | hydrogen production | 80 | 4 of 5 | ||
| 66794 | starch degradation | 80 | 8 of 10 | ||
| 66794 | methylglyoxal degradation | 80 | 4 of 5 | ||
| 66794 | threonine metabolism | 80 | 8 of 10 | ||
| 66794 | glycine betaine biosynthesis | 80 | 4 of 5 | ||
| 66794 | myo-inositol biosynthesis | 80 | 8 of 10 | ||
| 66794 | peptidoglycan biosynthesis | 80 | 12 of 15 | ||
| 66794 | glycogen metabolism | 80 | 4 of 5 | ||
| 66794 | cellulose degradation | 80 | 4 of 5 | ||
| 66794 | pyrimidine metabolism | 77.78 | 35 of 45 | ||
| 66794 | d-mannose degradation | 77.78 | 7 of 9 | ||
| 66794 | palmitate biosynthesis | 77.27 | 17 of 22 | ||
| 66794 | phenylalanine metabolism | 76.92 | 10 of 13 | ||
| 66794 | glycolysis | 76.47 | 13 of 17 | ||
| 66794 | isoleucine metabolism | 75 | 6 of 8 | ||
| 66794 | ketogluconate metabolism | 75 | 6 of 8 | ||
| 66794 | 6-hydroxymethyl-dihydropterin diphosphate biosynthesis | 75 | 6 of 8 | ||
| 66794 | dTDPLrhamnose biosynthesis | 75 | 6 of 8 | ||
| 66794 | acetate fermentation | 75 | 3 of 4 | ||
| 66794 | ppGpp biosynthesis | 75 | 3 of 4 | ||
| 66794 | glycogen biosynthesis | 75 | 3 of 4 | ||
| 66794 | pentose phosphate pathway | 72.73 | 8 of 11 | ||
| 66794 | photosynthesis | 71.43 | 10 of 14 | ||
| 66794 | degradation of pentoses | 71.43 | 20 of 28 | ||
| 66794 | Entner Doudoroff pathway | 70 | 7 of 10 | ||
| 66794 | degradation of sugar alcohols | 68.75 | 11 of 16 | ||
| 66794 | purine metabolism | 68.09 | 64 of 94 | ||
| 66794 | aspartate and asparagine metabolism | 66.67 | 6 of 9 | ||
| 66794 | CO2 fixation in Crenarchaeota | 66.67 | 6 of 9 | ||
| 66794 | formaldehyde oxidation | 66.67 | 2 of 3 | ||
| 66794 | octane oxidation | 66.67 | 2 of 3 | ||
| 66794 | glycolate and glyoxylate degradation | 66.67 | 4 of 6 | ||
| 66794 | NAD metabolism | 66.67 | 12 of 18 | ||
| 66794 | oxidative phosphorylation | 65.93 | 60 of 91 | ||
| 66794 | non-pathway related | 65.79 | 25 of 38 | ||
| 66794 | glutamate and glutamine metabolism | 64.29 | 18 of 28 | ||
| 66794 | d-xylose degradation | 63.64 | 7 of 11 | ||
| 66794 | histidine metabolism | 62.07 | 18 of 29 | ||
| 66794 | methionine metabolism | 57.69 | 15 of 26 | ||
| 66794 | tyrosine metabolism | 57.14 | 8 of 14 | ||
| 66794 | tetrahydrofolate metabolism | 57.14 | 8 of 14 | ||
| 66794 | ubiquinone biosynthesis | 57.14 | 4 of 7 | ||
| 66794 | propanol degradation | 57.14 | 4 of 7 | ||
| 66794 | cardiolipin biosynthesis | 57.14 | 4 of 7 | ||
| 66794 | degradation of hexoses | 55.56 | 10 of 18 | ||
| 66794 | alanine metabolism | 55.17 | 16 of 29 | ||
| 66794 | sulfopterin metabolism | 50 | 2 of 4 | ||
| 66794 | CMP-KDO biosynthesis | 50 | 2 of 4 | ||
| 66794 | ethanol fermentation | 50 | 1 of 2 | ||
| 66794 | lactate fermentation | 50 | 2 of 4 | ||
| 66794 | cis-vaccenate biosynthesis | 50 | 1 of 2 | ||
| 66794 | butanoate fermentation | 50 | 2 of 4 | ||
| 66794 | selenocysteine biosynthesis | 50 | 3 of 6 | ||
| 66794 | cysteine metabolism | 50 | 9 of 18 | ||
| 66794 | adipate degradation | 50 | 1 of 2 | ||
| 66794 | glycine metabolism | 50 | 5 of 10 | ||
| 66794 | leucine metabolism | 46.15 | 6 of 13 | ||
| 66794 | urea cycle | 46.15 | 6 of 13 | ||
| 66794 | sulfate reduction | 46.15 | 6 of 13 | ||
| 66794 | metabolism of disaccharids | 45.45 | 5 of 11 | ||
| 66794 | molybdenum cofactor biosynthesis | 44.44 | 4 of 9 | ||
| 66794 | lipid A biosynthesis | 44.44 | 4 of 9 | ||
| 66794 | degradation of sugar acids | 44 | 11 of 25 | ||
| 66794 | citric acid cycle | 42.86 | 6 of 14 | ||
| 66794 | lipid metabolism | 41.94 | 13 of 31 | ||
| 66794 | degradation of aromatic, nitrogen containing compounds | 41.67 | 5 of 12 | ||
| 66794 | arginine metabolism | 41.67 | 10 of 24 | ||
| 66794 | lipoate biosynthesis | 40 | 2 of 5 | ||
| 66794 | coenzyme M biosynthesis | 40 | 4 of 10 | ||
| 66794 | propionate fermentation | 40 | 4 of 10 | ||
| 66794 | creatinine degradation | 40 | 2 of 5 | ||
| 66794 | tryptophan metabolism | 39.47 | 15 of 38 | ||
| 66794 | vitamin B1 metabolism | 38.46 | 5 of 13 | ||
| 66794 | proline metabolism | 36.36 | 4 of 11 | ||
| 66794 | ascorbate metabolism | 36.36 | 8 of 22 | ||
| 66794 | arachidonic acid metabolism | 33.33 | 6 of 18 | ||
| 66794 | sphingosine metabolism | 33.33 | 2 of 6 | ||
| 66794 | acetyl CoA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | IAA biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | nitrate assimilation | 33.33 | 3 of 9 | ||
| 66794 | enterobactin biosynthesis | 33.33 | 1 of 3 | ||
| 66794 | flavin biosynthesis | 33.33 | 5 of 15 | ||
| 66794 | carotenoid biosynthesis | 31.82 | 7 of 22 | ||
| 66794 | androgen and estrogen metabolism | 31.25 | 5 of 16 | ||
| 66794 | lysine metabolism | 30.95 | 13 of 42 | ||
| 66794 | isoprenoid biosynthesis | 30.77 | 8 of 26 | ||
| 66794 | mevalonate metabolism | 28.57 | 2 of 7 | ||
| 66794 | glutathione metabolism | 28.57 | 4 of 14 | ||
| 66794 | dolichyl-diphosphooligosaccharide biosynthesis | 27.27 | 3 of 11 | ||
| 66794 | carnitine metabolism | 25 | 2 of 8 | ||
| 66794 | toluene degradation | 25 | 1 of 4 | ||
| 66794 | biotin biosynthesis | 25 | 1 of 4 | ||
| 66794 | methanogenesis from CO2 | 25 | 3 of 12 | ||
| 66794 | alginate biosynthesis | 25 | 1 of 4 | ||
| 66794 | cyclohexanol degradation | 25 | 1 of 4 | ||
| 66794 | phosphatidylethanolamine bioynthesis | 23.08 | 3 of 13 | ||
| 66794 | phenylpropanoid biosynthesis | 23.08 | 3 of 13 | ||
| 66794 | heme metabolism | 21.43 | 3 of 14 |
| Cat1 | Cat2 | Cat3 | |
|---|---|---|---|
| #Condition | #Anoxic (anaerobic) | - | |
| #Engineered | #Biodegradation | #Anaerobic digestor | |
| #Engineered | #Bioreactor | - | |
| #Engineered | #Waste | #Wastewater |
Global distribution of 16S sequence LC049585 (>99% sequence identity) for Flexilinea flocculi subclade from Microbeatlas ![]()
| Topic | Title | Authors | Journal | DOI | Year | |
|---|---|---|---|---|---|---|
| Phylogeny | Isolation and characterization of Flexilinea flocculi gen. nov., sp. nov., a filamentous, anaerobic bacterium belonging to the class Anaerolineae in the phylum Chloroflexi. | Sun L, Toyonaga M, Ohashi A, Matsuura N, Tourlousse DM, Meng XY, Tamaki H, Hanada S, Cruz R, Yamaguchi T, Sekiguchi Y | Int J Syst Evol Microbiol | 10.1099/ijsem.0.000822 | 2015 |
| #20215 | Parte, A.C., Sardà Carbasse, J., Meier-Kolthoff, J.P., Reimer, L.C. and Göker, M.: List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ. IJSEM ( DOI 10.1099/ijsem.0.004332 ) |
| #43788 | Liwei Sun, Mayu Toyonaga, Akiko Ohashi, Norihisa Matsuura, Dieter M. Tourlousse, Xian-Ying Meng, Hideyuki Tamaki, Satoshi Hanada, Rodrigo Cruz, Takashi Yamaguchi, Yuji Sekiguchi: Isolation and characterization of Flexilinea flocculi gen. nov., sp. nov., a filamentous, anaerobic bacterium belonging to the class Anaerolineae in the phylum Chloroflexi. IJSEM 66: 988 - 996 2016 ( DOI 10.1099/ijsem.0.000822 , PubMed 26637817 ) |
| #66794 | Antje Chang, Lisa Jeske, Sandra Ulbrich, Julia Hofmann, Julia Koblitz, Ida Schomburg, Meina Neumann-Schaal, Dieter Jahn, Dietmar Schomburg: BRENDA, the ELIXIR core data resource in 2021: new developments and updates. Nucleic Acids Res. 49: D498 - D508 2020 ( DOI 10.1093/nar/gkaa1025 , PubMed 33211880 ) |
| #67770 | Japan Collection of Microorganism (JCM) ; Curators of the JCM; |
| #69479 | João F Matias Rodrigues, Janko Tackmann,Gregor Rot, Thomas SB Schmidt, Lukas Malfertheiner, Mihai Danaila,Marija Dmitrijeva, Daniela Gaio, Nicolas Näpflin and Christian von Mering. University of Zurich.: MicrobeAtlas 1.0 beta . |
| #126262 | A. Lissin, I. Schober, J. F. Witte, H. Lüken, A. Podstawka, J. Koblitz, B. Bunk, P. Dawyndt, P. Vandamme, P. de Vos, J. Overmann, L. C. Reimer: StrainInfo—the central database for linked microbial strain identifiers. ( DOI 10.1093/database/baaf059 ) |
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