Abstract
The family Cytophagaceae, which spans at least 25 genera and 80 species, is one of the largest families in the phylum Bacteroidetes. The members of the family are diverse in terms of physiology and habitat, but some common properties can be identified. Members of the family Cytophagaceae are commonly isolated from marine, freshwater, and terrestrial habitats. All known members are heterotrophic and most are aerobic with primarily respiratory metabolism. Menaquinones of type 7 (MK7) are the major respiratory quinones, a feature that they share with other members of the class Cytophagia but that distinguishes them from physiologically similar bacteria from the family Flavobacteriaceae, which have menaquinones of type 6 (MK6). Most species have rod-shaped cells, with some exhibiting filamentation and others forming curved, spiral, or ring-shaped cells. Most species are pigmented yellow, orange, red, or pink as a result of flexirubin pigments, carotenoids, or both. Movement over surfaces by gliding motility is common but not universal, whereas other forms of motility have apparently not been observed. Most species are mesophilic, but a few are psychrophilic. Many members of the family digest macromolecules such as polysaccharides or proteins. Members of the type genus, Cytophaga, are proficient at digestion of insoluble cellulose, as are members of the closely related genus Sporocytophaga. Cellulose utilization by members of the genus Cytophaga appears to involve an apparently novel collection of glycosyl hydrolases. Obvious cellobiohydrolases that are often associated with cellulose utilization by other bacteria are lacking. Cellulose utilization may involve novel cell-surface machinery for initial digestion of cellulose and for uptake of the resulting cellodextrins across the outer membrane. Other noteworthy members of the family include gliding bacteria of the genera Flexibacter and Microscilla, spiral and curved bacteria of the genera Arcicella, Flectobacillus, Larkinella, Runella, and Spirosoma, desiccation and radiation resistant members of the genus Hymenobacter, and strongly adherent bacteria of the genus Adhaeribacter.
Phylogenetic analyses based on 16S rRNA sequences revealed multiple potential problems with the family as currently described. The family Cytophagaceae appears to encompass two divergent clades of bacteria that are not well resolved from members of the families Cyclobacteriaceae and Flammeovirgaceae. A restructuring of the family Cytophagaceae may be necessary, either splitting it into two or more families or combining it with the families Cyclobacteriaceae and Flammeovirgaceae.
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Abaydulla G, Luo X, Shi J, Peng F, Liu M, Wang Y, Dai J, Fang C (2012) Rufibacter tibetensis gen. nov., sp. nov., a novel member of the family Cytophagaceae isolated from soil. Antonie Van Leeuwenhoek 101:725–731
Abt B, Teshima H, Lucas S, Lapidus A, Del Rio TG, Nolan M, Tice H, Cheng JF, Pitluck S, Liolios K, Pagani I, Ivanova N, Mavromatis K, Pati A, Tapia R, Han C, Goodwin L, Chen A, Palaniappan K, Land M, Hauser L, Chang YJ, Jeffries CD, Rohde M, Goker M, Tindall BJ, Detter JC, Woyke T, Bristow J, Eisen JA, Markowitz V, Hugenholtz P, Klenk HP, Kyrpides NC (2011) Complete genome sequence of Leadbetterella byssophila type strain (4 M15). Stand Genomic Sci 4:2–12
Achenbach H, Kohl W, Wachter W, Reichenbach H (1978) Investigations of the pigments from Cytophaga johnsonae Cy jl. New flexirubin-type pigments. Arch Microbiol 117:253–257
Alain K, Tindall BJ, Catala P, Intertaglia L, Lebaron P (2010) Ekhidna lutea gen. nov., sp. nov., a member of the phylum Bacteroidetes isolated from the South East Pacific Ocean. Int J Syst Evol Microbiol 60:2972–2978
Anderson KL, Salyers AA (1989) Biochemical evidence that starch breakdown by Bacteroides thetaiotaomicron involves outer membrane starch-binding sites and periplasmic starch-degrading enzymes. J Bacteriol 171:3192–3198
Baik KS, Kim MS, Kim EM, Kim HR, Seong CN (2007a) Dyadobacter koreensis sp. nov., isolated from fresh water. Int J Syst Evol Microbiol 57:1227–1231
Baik KS, Kim MS, Park SC, Lee DW, Lee SD, Ka JO, Choi SK, Seong CN (2007b) Spirosoma rigui sp. nov., isolated from fresh water. Int J Syst Evol Microbiol 57:2870–2873
Baik KS, Seong CN, Moon EY, Park YD, Yi H, Chun J (2006) Hymenobacter rigui sp. nov., isolated from wetland freshwater. Int J Syst Evol Microbiol 56:2189–2192
Bernardet J-F, Segers P, Vancanneyt M, Berthe F, Kersters K, Vandamme P (1996) Cutting a gordian knot: Emended classification and description of the genus Flavobacterium, and proposal of Flavobacterium hydatis nom. nov. (Basonym, Cytophaga aquatilis Strohl and Tait 1978). Int J Syst Bacteriol 46:128–148
Bernardet JF, Nakagawa Y, Holmes B (2002) Proposed minimal standards for describing new taxa of the family Flavobacteriaceae and emended description of the family. Int J Syst Evol Microbiol 52:1049–1070
Bowman JP, Nichols CM, Gibson JA (2003) Algoriphagus ratkowskyi gen. nov., sp. nov., Brumimicrobium glaciale gen. nov., sp. nov., Cryomorpha ignava gen. nov., sp. nov. and Crocinitomix catalasitica gen. nov., sp. nov., novel flavobacteria isolated from various polar habitats. Int J Syst Evol Microbiol 53:1343–1355
Buczolits S, Busse HJ (2011) Genus IX: Hymenobacter. In: Krieg NR, Staley JT, Brown DR et al (eds) Bergey’s manual of systematic bacteriology, vol 4. Springer, New York, pp 397–404
Buczolits S, Denner EB, Kampfer P, Busse HJ (2006) Proposal of Hymenobacter norwichensis sp. nov., classification of ‘Taxeobacter ocellatus’, ‘Taxeobacter gelupurpurascens’ and ‘Taxeobacter chitinovorans’ as Hymenobacter ocellatus sp. nov., Hymenobacter gelipurpurascens sp. nov. and Hymenobacter chitinivorans sp. nov., respectively, and emended description of the genus Hymenobacter Hirsch et al. 1999. Int J Syst Evol Microbiol 56:2071–2078
Buczolits S, Denner EB, Vybiral D, Wieser M, Kampfer P, Busse HJ (2002) Classification of three airborne bacteria and proposal of Hymenobacter aerophilus sp. nov. Int J Syst Evol Microbiol 52:445–456
Chang WTH, Thayer DW (1977) The cellulase system of a Cytophaga species. Can J Microbiol 23:1285–1292
Chaturvedi P, Reddy GS, Shivaji S (2005) Dyadobacter hamtensis sp. nov., from Hamta glacier, located in the Himalayas, India. Int J Syst Evol Microbiol 55:2113–2117
Chelius MK, Triplett EW (2000) Dyadobacter fermentans gen. nov., sp. nov., a novel gram-negative bacterium isolated from surface-sterilized Zea mays stems. Int J Syst Evol Microbiol 50 Pt 2:751–758
Christensen PJ (1977) The history, biology, and taxonomy of the Cytophaga group. Can J Microbiol 23:1599–1653
Chun J, Kang JY, Joung Y, Kim H, Joh K, Jahng KY (2013) Dyadobacter jejuensis sp. nov., isolated from seawater. Int J Syst Evol Microbiol 63:1788–1792
Chung AP, Lopes A, Nobre MF, Morais PV (2010) Hymenobacter perfusus sp. nov., Hymenobacter flocculans sp. nov. and Hymenobacter metalli sp. nov. three new species isolated from an uranium mine waste water treatment system. Syst Appl Microbiol 33:436–443
Collins MD, Hutson RA, Grant IR, Patterson MF (2000) Phylogenetic characterization of a novel radiation-resistant bacterium from irradiated pork: description of Hymenobacter actinosclerus sp. nov. Int J Syst Evol Microbiol 50 pt 2:731–734
Copeland A, Zhang X, Misra M, Lapidus A, Nolan M, Lucas S, Deshpande S, Cheng JF, Tapia R, Goodwin LA, Pitluck S, Liolios K, Pagani I, Ivanova N, Mikhailova N, Pati A, Chen A, Palaniappan K, Land M, Hauser L, Pan C, Jeffries CD, Detter JC, Brambilla EM, Rohde M, Djao OD, Goker M, Sikorski J, Tindall BJ, Woyke T, Bristow J, Eisen JA, Markowitz V, Hugenholtz P, Kyrpides NC, Klenk HP, Mavromatis K (2012) Complete genome sequence of the aquatic bacterium Runella slithyformis type strain (LSU 4(T)). Stand Genomic Sci 6:145–154
Dai J, Wang Y, Zhang L, Tang Y, Luo X, An H, Fang C (2009) Hymenobacter tibetensis sp. nov., a UV-resistant bacterium isolated from Qinghai-Tibet plateau. Syst Appl Microbiol 32:543–548
Dastager SG, Deepa CK, Pandey A (2011) Plant growth promoting potential of Pontibacter niistensis in cowpea (Vigna unguiculata (L.) Walp.). Appl Soil Ecol 49:250–255
Dastager SG, Raziuddin QS, Deepa CK, Li WJ, Pandey A (2010) Pontibacter niistensis sp. nov., isolated from forest soil. Int J Syst Evol Microbiol 60:2867–2870
Dong Z, Guo X, Zhang X, Qiu F, Sun L, Gong H, Zhang F (2007) Dyadobacter beijingensis sp. nov., isolated from the rhizosphere of turf grasses in China. Int J Syst Evol Microbiol 57:862–865
Drijber RA, McGill WB (1992) A modification of the method using cellulose overlay agar to isolate and purify cellulolytic cytophagas from enrichment culture. Can J Microbiol 38:687–689
Drijber RA, McGill WB (1997) Cytophaga hutchinsonii ATCC 33406 contains a structural variant of the sulfonolipid N-acylcapnine. Can J Microbiol 43:689–693
Eisenberg J (ed) (1891) Bacteriologische diagnostik: Hilfstabellen zum gebrauche beim praktischen arbeiten. Leopold Voss, Hamburg, p 212
Fahraeus G (1947) Studies on the cellulose decomposition by Cytophaga. Symb Bot Ups 9:1–128
Fuhrman JA, Schwalbach MS, Stingl U (2008) Proteorhodopsins: an array of physiological roles? Nat Rev Microbiol 6:488–494
Grace JB (1951) The life cycle of Sporocytophaga. J Gen Microbiol 5:519–524
Grote M, O’malley MA (2011) Enlightening the life sciences: the history of halobacterial and microbial rhodopsin research. FEMS Microbiol Rev 35:1082–1099
Hirsch P, Ludwig W, Hethke C, Sittig M, Hoffmann B, Gallikowski CA (1998) Hymenobacter roseosalivarius gen. nov., sp. nov. from continental Antartica soils and sandstone: bacteria of the Cytophaga/Flavobacterium/Bacteroides line of phylogenetic descent. Syst Appl Microbiol 21:374–383
Holt SC, Leadbetter ER (1967) Fine structure of Sporocytophaga myxococcoides. Arch Mikrobiol 57:199–213
Hosoya S, Yokota A (2007) Reclassification of Flexibacter aggregans (Lewin 1969) Leadbetter 1974 as a later heterotypic synonym of Flexithrix dorotheae Lewin 1970. Int J Syst Evol Microbiol 57:1086–1088
Hutchinson HB, Clayton J (1919) On the decomposition of cellulose by an aerobic organism (Spirochaeta cytophaga, n. sp.). J Agric Sci 9:143–173
Imsenecki A, Solntzeva L (1936) On aerobic cellulose-decomposing bacteria. Bull Acad Sci, URSS 6:1115–1172
Ji X, Xu Y, Zhang C, Chen N, Lu X (2012) A new locus affects cell motility, cellulose binding, and degradation by Cytophaga hutchinsonii. Appl Microbiol Biotechnol 96:161–170
Kampfer P, Young CC, Sridhar KR, Arun AB, Lai WA, Shen FT, Rekha PD (2006) Transfer of [Flexibacter] sancti, [Flexibacter] filiformis, [Flexibacter] japonensis and [Cytophaga] arvensicola to the genus Chitinophaga and description of Chitinophaga skermanii sp. nov. Int J Syst Evol Microbiol 56:2223–2228
Kang JY, Joung Y, Chun J, Kim H, Joh K, Jahng KY (2013) Pontibacter saemangeumensis sp. nov., isolated from sea water of South Korea. Int J Syst Evol Microbiol 63:565–569
Klassen JL, Foght JM (2008) Differences in carotenoid composition among hymenobacter and related strains support a tree-like model of carotenoid evolution. Appl Environ Microbiol 74:2016–2022
Krieg NR, Ludwig W, Euzeby J, Whitman WB (2011) Phylum XIV. Bacteroidetes phyl. nov. In: Krieg NR, Staley JT, Brown DR et al (eds) Bergey’s manual of systematic bacteriology, vol 4. Springer, New York, pp 25–469
Krzemieniewska H (1933) Contribution a l’etude du genre Cytophaga (Winogradsky). Arch Microbiol 4:394–408
Lail K, Sikorski J, Saunders E, Lapidus A, Glavina Del Rio T, Copeland A, Tice H, Cheng JF, Lucas S, Nolan M, Bruce D, Goodwin L, Pitluck S, Ivanova N, Mavromatis K, Ovchinnikova G, Pati A, Chen A, Palaniappan K, Land M, Hauser L, Chang YJ, Jeffries CD, Chain P, Brettin T, Detter JC, Schutze A, Rohde M, Tindall BJ, Goker M, Bristow J, Eisen JA, Markowitz V, Hugenholtz P, Kyrpides NC, Klenk HP, Chen F (2010) Complete genome sequence of Spirosoma linguale type strain (1). Stand Genomic Sci 2:176–185
Lang E, Lapidus A, Chertkov O, Brettin T, Detter JC, Han C, Copeland A, Glavina Del Rio T, Nolan M, Chen F, Lucas S, Tice H, Cheng JF, Land M, Hauser L, Chang YJ, Jeffries CD, Kopitz M, Bruce D, Goodwin L, Pitluck S, Ovchinnikova G, Pati A, Ivanova N, Mavrommatis K, Chen A, Palaniappan K, Chain P, Bristow J, Eisen JA, Markowitz V, Hugenholtz P, Goker M, Rohde M, Kyrpides NC, Klenk HP (2009) Complete genome sequence of Dyadobacter fermentans type strain (NS114). Stand Genomic Sci 1:133–140
Lanyi JK, Balashov SP (2008) Xanthorhodopsin: a bacteriorhodopsin-like proton pump with a carotenoid antenna. BBA Bioenerg 1777:684–688
Larkin JM (1989) Nonphotosynthetic, nonfruiting gliding bacteria. In: Staley JT, Bryant MP, Pfennig N, Holt JG (eds) Bergey’s manual of systematic bacteriology, vol 3. Williams and Wilkins, Baltimore, pp 2010–2138
Larkin JM, Borrall R (1984) Family I. Spirosomaceae. In: Krieg NR, Holt JG (eds) Bergey’s manual of systematic bacteriology, vol 1. Williams and Wilkins, Baltimore, pp 125–126
Larkin JM, Williams PM (1978) Runella slithyformis gen. nov., sp. nov., a curved, nonflexible, pink bacterium. Int J Syst Bacteriol 28:32–36
Larkin JM, Williams PM, Taylor R (1977) Taxonomy of the genus Microcyclus Orskov 1928: reintroduction and emendation of the genus Spirosoma Migula 1894 and proposal of a new genus Flectobacillus. Int J Syst Bacteriol 27:147–156
Leadbetter ER (2011) Genus XVII: Sporocytophaga. In: Krieg NR, Staley JT, Brown DR et al (eds) Bergey’s manual of systematic bacteriology, vol 4. Springer, New York, p 418
Lee M, Woo SG, Park J, Yoo SA (2010) Dyadobacter soli sp. nov., a starch-degrading bacterium isolated from farm soil. Int J Syst Evol Microbiol 60:2577–2582
Li X, Chen F (1998) Improvement in isolation of gliding bacteria by the elimination of soluble sugars. Biotechnol Tech 12:343–345
Ludwig W, Euzeby J, Whitman WB (2011) Road map of the phyla of the phyla Bacteroidetes, Spirochaetes, Tenericutes (Mollicutes), Acidobacteria, Fibrobacteres, Fusobacteria, Dictyoglomi, Gemmatimonadetes, Lentisphaerae, Verrucomicrobia, Chlamydiae, and Planctomycetes. In: Krieg NR, Staley JT, Brown DR et al (eds) Bergey’s manual of systematic bacteriology, vol 4. Springer, New York, pp 1–19
Lynd LR, Weimer PJ, van Zyl WH, Pretorius IS (2002) Microbial cellulose utilization: fundamentals and biotechnology. Microbiol Mol Biol Rev 66:506–577
Manter DK, Delgado JA, Holm DG, Stong RA (2010) Pyrosequencing reveals a highly diverse and cultivar-specific bacterial endophyte community in potato roots. Microb Ecol 60:157–166
McBride MJ (2001) Bacterial gliding motility: multiple mechanisms for cell movement over surfaces. Annu Rev Microbiol 55:49–75
McBride MJ, Baker SA (1996) Development of techniques to genetically manipulate members of the genera Cytophaga, Flavobacterium, Flexibacter, and Sporocytophaga. Appl Environ Microbiol 62:3017–3022
McBride MJ, Kempf MJ (1996) Development of techniques for the genetic manipulation of the gliding bacterium Cytophaga johnsonae. J Bacteriol 178:583–590
McBride MJ, Zhu Y (2013) Gliding motility and por secretion system genes are widespread among members of the phylum Bacteroidetes. J Bacteriol 195:270–278
Migula W (1894) Uber ein neues system der bakterien. Arb Bakteriol Inst Karlsruhe 1:235–238
Munoz R, Yarza P, Ludwig W, Euzeby J, Amann R, Schleifer KH, Glockner FO, Rossello-Mora R (2011) Release LTPs104 of the all-species living tree. Syst Appl Microbiol 34:169–170
Nakagawa Y (2011) Family I: Cytophagaceae. In: Krieg NR, Staley JT, Brown DR et al (eds) Bergey’s manual of systematic bacteriology, vol 4. Springer, New York, pp 371–423
Nakagawa Y, Sakane T, Suzuki M, Hatano K (2002) Phylogenetic structure of the genera Flexibacter, Flexithrix, and Microscilla deduced from 16S rRNA sequence analysis. J Gen Appl Microbiol 48:155–165
Nakagawa Y, Yamasato K (1993) Phylogenetic diversity of the genus Cytophaga revealed by 16S rRNA sequencing and menaquinone analysis. J Gen Microbiol 139 Pt 6:1155–1161
Nakagawa Y, Yamasato K (1996) Emendation of the genus Cytophaga and transfer of Cytophaga agarovorans and Cytophaga salmonicolor to Marinilabilia gen. nov.: phylogenetic analysis of the Flavobacterium-Cytophaga complex. Int J Syst Bacteriol 46:599–603
Nedashkovskaya OI, Kim SB, Suzuki M, Shevchenko LS, Lee MS, Lee KH, Park MS, Frolova GM, Oh HW, Bae KS, Park HY, Mikhailov VV (2005) Pontibacter actiniarum gen. nov., sp. nov., a novel member of the phylum ‘Bacteroidetes’, and proposal of Reichenbachiella gen. nov. as a replacement for the illegitimate prokaryotic generic name Reichenbachia Nedashkovskaya et al. 2003. Int J Syst Evol Microbiol 55:2583–2588
Nedashkovskaya OI, Ludwig W (2011) Family I: Cyclobacteriaceae. In: Krieg NR, Staley JT, Brown DR et al (eds) Bergey’s manual of systematic bacteriology, vol 4. Springer, New York, pp 423–441
Nelson SS, Bollampalli S, McBride MJ (2008) SprB is a cell surface component of the Flavobacterium johnsoniae gliding motility machinery. J Bacteriol 190:2851–2857
Nikitin DI, Strompl C, Oranskaya MS, Abraham WR (2004) Phylogeny of the ring-forming bacterium Arcicella aquatica gen. nov., sp. nov. (ex Nikitin et al. 1994), from a freshwater neuston biofilm. Int J Syst Evol Microbiol 54:681–684
Oren A (2006) The genera Rhodothermus, Thermonema, Hymenobacter and Salinibacter. In: Dworkin M, Falkow S, Rosenberg E, Schleifer KH, Stackebrandt E (eds) The prokaryotes, vol 7. Springer, New York, pp 712–738
Pringsheim EG (1951) The Vitreoscillaceae; a family of colourless, gliding, filamentous organisms. J Gen Microbiol 5:124–149
Rainey FA, Ray K, Ferreira M, Gatz BZ, Nobre MF, Bagaley D, Rash BA, Park MJ, Earl AM, Shank NC, Small AM, Henk MC, Battista JR, Kampfer P, da Costa MS (2005) Extensive diversity of ionizing-radiation-resistant bacteria recovered from Sonoran Desert soil and description of nine new species of the genus Deinococcus obtained from a single soil sample. Appl Environ Microbiol 71:5225–5235
Raj HD, Maloy SR (1990) Family Spirosomaceae: gram-negative ring-forming aerobic bacteria. Crit Rev Microbiol 17:329–364
Reasoner DJ, Geldreich EE (1985) A new medium for the enumeration and subculture of bacteria from potable water. Appl Environ Microbiol 49:1–7
Reddy GS, Garcia-Pichel F (2005) Dyadobacter crusticola sp. nov., from biological soil crusts in the Colorado Plateau, USA, and an emended description of the genus Dyadobacter Chelius and Triplett 2000. Int J Syst Evol Microbiol 55:1295–1299
Reeves AR, D’Elia JN, Frias J, Salyers AA (1996) A Bacteroides thetaiotaomicron outer membrane protein that is essential for utilization of maltooligosaccharides and starch. J Bacteriol 178:823–830
Reichenbach H (1989) Family I. Cytophagaceae. In: Staley JT, Bryant MP, Pfennig N, Holt JG (eds) Bergey’s manual of systematic bacteriology, vol 3. Williams and Wilkins, Baltimore, pp 2013–2082
Reichenbach H (1992) The order Cytophagales. In: Balows A, Truper HG, Dworkin M, Harder W, Schleifer KM (eds) The prokaryotes. Springer, New York, pp 3631–3675
Reisberg EE, Hildebrandt U, Riederer M, Hentschel U (2012) Phyllosphere bacterial communities of trichome-bearing and trichomeless Arabidopsis thaliana leaves. Antonie Van Leeuwenhoek 101:551–560
Rhodes RG, Samarasam MN, Shrivastava A, van Baaren JM, Pochiraju S, Bollampalli S, McBride MJ (2010) Flavobacterium johnsoniae gldN and gldO are partially redundant genes required for gliding motility and surface localization of SprB. J Bacteriol 192:1201–1211
Rhodes RG, Samarasam MN, Van Groll EJ, McBride MJ (2011) Mutations in Flavobacterium johnsoniae sprE result in defects in gliding motility and protein secretion. J Bacteriol 193:5322–5327
Rickard AH, Stead AT, O’May GA, Lindsay S, Banner M, Handley PS, Gilbert P (2005) Adhaeribacter aquaticus gen. nov., sp. nov., a Gram-negative isolate from a potable water biofilm. Int J Syst Evol Microbiol 55:821–829
Riviere J (1961) Isolation and purification of aerobic cellulolytic soil bacteria. II. Isolation and description of a new Arthrobacter species associated with Sporocytophaga myxococcoides. Ann Inst Pasteur 101:793–800
Salyers AA, Bonheyo G, Shoemaker NB (2000) Starting a new genetic system: lessons from bacteroides. Methods 20:35–46
Salyers AA, Reeves A, D’Elia J (1996) Solving the problem of how to eat something as big as yourself: diverse bacterial strategies for degrading polysaccharides. J Ind Microbiol 17:470–476
Sato K, Naito M, Yukitake H, Hirakawa H, Shoji M, McBride MJ, Rhodes RG, Nakayama K (2010) A protein secretion system linked to bacteroidete gliding motility and pathogenesis. Proc Natl Acad Sci USA 107:276–281
Shipman JA, Berleman JE, Salyers AA (2000) Characterization of four outer membrane proteins involved in binding starch to the cell surface of Bacteroides thetaiotaomicron. J Bacteriol 182:5365–5372
Shrivastava A, Rhodes RG, Pochiraju S, Nakane D, McBride MJ (2012) Flavobacterium johnsoniae RemA is a mobile cell-surface lectin involved in gliding. J Bacteriol 194:3678–3688
Sijpesteijn AK, Fahraeus G (1949) Adaptation of Sporocytophaga myxococcoides to sugars. J Gen Microbiol 3:224–235
Soriano S (1945) Un nuevo orden de bacterias: Flexibacteriales. Cienc Invest 1:92–93
Speyer E (1953) Studies on Sporocytophaga myxococcoides, Stanier 1940. Arch Mikrobiol 18:245–272
Stanier RY (1940) Studies on the cytophagas. J Bacteriol 40:619–635
Stanier RY (1941) Studies on marine agar-digesting bacteria. J Bacteriol 42:527–559
Stanier RY (1942) The cytophaga group: a contribution to the biology of myxobacteria. Bacteriol Rev 6:143–196
Stanier RY (1947) Studies on non-fruiting myxobacteria. I. Cytophaga johnsonae, N. Sp., A chitin-decomposing myxobacterium. J Bacteriol 53:297–315
Stapp C, Bortels H (1934) Mikrobiologische untersuchungen uber die zersetzung von waldstreu. Zent Bakteriol 90:28–69
Suzuki M, Nakagawa Y, Harayama S, Yamamoto S (2001) Phylogenetic analysis and taxonomic study of marine Cytophaga-like bacteria: proposal for Tenacibaculum gen. nov. with Tenacibaculum maritimum comb. nov. and Tenacibaculum ovolyticum comb. nov., and description of Tenacibaculum mesophilum sp. nov. and Tenacibaculum amylolyticum sp. nov. Int J Syst Evol Microbiol 51:1639–1652
Takahashi M, Suzuki K, Nakagawa Y (2006) Emendation of the genus Flammeovirga and Flammeovirga aprica with the proposal of Flammeovirga arenaria nom. rev., comb. nov. and Flammeovirga yaeyamensis sp. nov. Int J Syst Evol Microbiol 56:2095–2100
Tang Y, Dai J, Zhang L, Mo Z, Wang Y, Li Y, Ji S, Fang C, Zheng C (2009) Dyadobacter alkalitolerans sp. nov., isolated from desert sand. Int J Syst Evol Microbiol 59:60–64
Tian SP, Wang YX, Hu B, Zhang XX, Xiao W, Chen Y, Lai YH, Wen ML, Cui XL (2010) Litoribacter ruber gen. nov., sp. nov., an alkaliphilic, halotolerant bacterium isolated from a soda lake sediment. Int J Syst Evol Microbiol 60:2996–3001
Uenoyama A, Kusumoto A, Miyata M (2004) Identification of a 349-kilodalton protein (Gli349) responsible for cytadherence and glass binding during gliding of Mycoplasma mobile. J Bacteriol 186:1537–1545
Ugalde JA, Podell S, Narasingarao P, Allen EE (2011) Xenorhodopsins, an enigmatic new class of microbial rhodopsins horizontally transferred between archaea and bacteria. Biol Direct 6:52
Vancanneyt M, Nedashkovskaya OI, Snauwaert C, Mortier S, Vandemeulebroecke K, Hoste B, Dawyndt P, Frolova GM, Janssens D, Swings J (2006) Larkinella insperata gen. nov., sp. nov., a bacterium of the phylum ‘Bacteroidetes’ isolated from water of a steam generator. Int J Syst Evol Microbiol 56:237–241
Verma JP, Martin HH (1967a) Chemistry and ultrastructure of surface layers in primitive myxobacteria: Cytophaga hutchinsonii and Sporocytophaga myxococcoides. Folia Microbiol (Praha) 12:248–254
Verma JP, Martin HH (1967b) On the surface of myxobacteria. I. Chemistry and morphology of the cell walls of Cytophaga hutchinsonii and Sporocytophaga myxococcoides. Arch Mikrobiol 59:355–380
Walker E, Warren FL (1938) Decomposition of cellulose by Cytophaga I. Biochem J 32:31–43
Warren RA (1996) Microbial hydrolysis of polysaccharides. Annu Rev Microbiol 50:183–212
Weon HY, Kwon SW, Son JA, Kim SJ, Kim YS, Kim BY, Ka JO (2010) Adhaeribacter aerophilus sp. nov., Adhaeribacter aerolatus sp. nov. and Segetibacter aerophilus sp. nov., isolated from air samples. Int J Syst Evol Microbiol 60:2424–2429
Willumsen PA, Johansen JE, Karlson U, Hansen BM (2005) Isolation and taxonomic affiliation of N-heterocyclic aromatic hydrocarbon-transforming bacteria. Appl Microbiol Biotechnol 67:420–428
Winogradsky S (1929) E’tudes sur la microbiologie du sol. Ann Inst Pasteur 43:549–633
Xie G, Bruce DC, Challacombe JF, Chertkov O, Detter JC, Gilna P, Han CS, Lucas S, Misra M, Myers GL, Richardson P, Tapia R, Thayer N, Thompson LS, Brettin TS, Henrissat B, Wilson DB, McBride MJ (2007) Genome sequence of the cellulolytic gliding bacterium Cytophaga hutchinsonii. Appl Environ Microbiol 73:3536–3546
Xu Y, Ji X, Chen N, Li P, Liu W, Lu X (2012) Development of replicative oriC plasmids and their versatile use in genetic manipulation of Cytophaga hutchinsonii. Appl Microbiol Biotechnol 93:697–705
Yarza P, Ludwig W, Euzeby J, Amann R, Schleifer KH, Glockner FO, Rossello-Mora R (2010) Update of the All-Species Living Tree Project based on 16S and 23S rRNA sequence analyses. Syst Appl Microbiol 33:291–299
Zhang JY, Liu XY, Liu SJ (2009) Adhaeribacter terreus sp. nov., isolated from forest soil. Int J Syst Evol Microbiol 59:1595–1598
Zhang Q, Liu C, Tang Y, Zhou G, Shen P, Fang C, Yokota A (2007) Hymenobacter xinjiangensis sp. nov., a radiation-resistant bacterium isolated from the desert of Xinjiang, China. Int J Syst Evol Microbiol 57:1752–1756
Zhou Y, Wang X, Liu H, Zhang KY, Zhang YQ, Lai R, Li WJ (2007) Pontibacter akesuensis sp. nov., isolated from a desert soil in China. Int J Syst Evol Microbiol 57:321–325
Zhu Y, Li H, Zhou H, Chen G, Liu W (2010) Cellulose and cellulodextrin utilization by the cellulolytic bacterium Cytophaga hutchinsonii. Bioresour Technol 101:6432–6437
Zhu Y, Zhou H, Bi Y, Zhang W, Chen G, Liu W (2013) Characterization of a family 5 glycoside hydrolase isolated from the outer membrane of cellulolytic Cytophaga hutchinsonii. Appl Microbiol Biotechnol 97:3925–3937
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McBride, M.J., Liu, W., Lu, X., Zhu, Y., Zhang, W. (2014). The Family Cytophagaceae . In: Rosenberg, E., DeLong, E.F., Lory, S., Stackebrandt, E., Thompson, F. (eds) The Prokaryotes. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-38954-2_382
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DOI: https://doi.org/10.1007/978-3-642-38954-2_382
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