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Pseudomonas hutmensis sp. nov., a New Fluorescent Member of Pseudomonas putida Group

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Abstract

A rod-shaped, Gram-negative and aerobic bacterium, strain XWS2, was isolated from rhizosphere soil of a camphor tree in Hubei University of Chinese Medicine Huangjiahu Campus, Wuhan, China. Cells grew at 4–37 °C (optimum 28 °C), pH 5.0–9.0 (optimum 7.0) and with 0–5% NaCl (optimum 1%). Colonies growing on tryptone soybean agar are round, beige in color and approximately 2 mm in diameter after 24 h incubation at 28 °C. Pellicle formation during liquid culture and strong fluorescent pigment production on King’s B medium are typical features of strain XWS2. The genome of XWS2 is 6,170,117 bp, containing 5682 predicted genes and 4770 genes are functionally annotated. Phylogenetic analysis based on 16S rRNA sequence showed that strain XWS2 formed an independent branch within the Pseudomonas putida group, with P. putida NBRC 14164T (99.86% similarity) and P. alkylphenolica KL28T (99.36% similarity) as the most closely related type strains. Genome sequence analysis based on average nucleotide identity and digital DNA–DNA hybridization are below the threshold values for species delineation. Phenotypic characteristics, physiological and biochemical tests also supported the strain represents a separate novel species within the Pseudomonas genus. The name Pseudomonas hutmensis sp. nov. is proposed, with type strain XWS2T (= CCTCC AB 2018189 T = KACC 19898T).

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References

  1. Peix A, Ramirez-Bahena MH, Velazquez E (2018) The current status on the taxonomy of Pseudomonas revisited: an update. Infect Genet Evol 57:106–116. https://doi.org/10.1016/j.meegid.2017.10.026

    Article  PubMed  Google Scholar 

  2. Azhar EI, Papadioti A, Bibi F, Ashshi AM, Raoult D, Angelakis E (2017) ‘Pseudomonas saudimassiliensis’ sp. nov. a new bacterial species isolated from air samples in the urban environment of Makkah, Saudi Arabia. New Microbes New Infect 16:43–44. https://doi.org/10.1016/j.nmni.2016.12.021

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Mulet M, Sanchez D, Rodriguez AC, Nogales B, Bosch R, Busquets A, Gomila M, Lalucat J, Garcia-Valdes E (2018) Pseudomonas gallaeciensis sp. nov., isolated from crude-oil-contaminated intertidal sand samples after the Prestige oil spill. Syst Appl Microbiol 41(4):340–347. https://doi.org/10.1016/j.syapm.2018.03.008

    Article  CAS  PubMed  Google Scholar 

  4. Kaminski MA, Furmanczyk EM, Sobczak A, Dziembowski A, Lipinski L (2018) Pseudomonas silesiensis sp. nov. strain A3(T) isolated from a biological pesticide sewage treatment plant and analysis of the complete genome sequence. Syst Appl Microbiol 41(1):13–22. https://doi.org/10.1016/j.syapm.2017.09.002

    Article  CAS  PubMed  Google Scholar 

  5. See-Too WS, Salazar S, Ee R, Convey P, Chan KG, Peix A (2017) Pseudomonas versuta sp. nov., isolated from Antarctic soil. Syst Appl Microbiol 40(4):191–198. https://doi.org/10.1016/j.syapm.2017.03.002

    Article  CAS  PubMed  Google Scholar 

  6. Sun J, Wang W, Ying Y, Zhu X, Liu J, Hao J (2018) Pseudomonas profundi sp. nov., isolated from deep-sea water. Int J Syst Evol Microbiol 68(5):1776–1780. https://doi.org/10.1099/ijsem.0.002748

    Article  CAS  PubMed  Google Scholar 

  7. Wei Y, Mao H, Xu Y, Zou W, Fang J, Blom J (2018) Pseudomonas abyssi sp. nov., isolated from the abyssopelagic water of the Mariana Trench. Int J Syst Evol Microbiol 68(8):2462–2467. https://doi.org/10.1099/ijsem.0.002785

    Article  PubMed  Google Scholar 

  8. Yu XY, Zhai JY, Wu C, Zhang CY, Shi JY, Ding LX, Wu M (2018) Pseudomonas pharmafabricae sp. nov., isolated from pharmaceutical wastewater. Curr Microbiol 75(9):1119–1125. https://doi.org/10.1007/s00284-018-1495-z

    Article  CAS  PubMed  Google Scholar 

  9. Timilsina S, Minsavage GV, Preston J, Newberry EA, Paret ML, Goss EM, Jones JB, Vallad GE (2018) Pseudomonas floridensis sp. nov., a bacterial pathogen isolated from tomato. Int J Syst Evol Microbiol 68(1):64–70. https://doi.org/10.1099/ijsem.0.002445

    Article  PubMed  Google Scholar 

  10. Busquets A, Gomila M, Beiki F, Mulet M, Rahimian H, Garcia-Valdes E, Lalucat J (2017) Pseudomonas caspiana sp. nov., a citrus pathogen in the Pseudomonas syringae phylogenetic group. Syst Appl Microbiol 40(5):266–273. https://doi.org/10.1016/j.syapm.2017.04.002

    Article  PubMed  Google Scholar 

  11. Saati-Santamaria Z, Lopez-Mondejar R, Jimenez-Gomez A, Diez-Mendez A, Vetrovsky T, Igual JM, Velazquez E, Kolarik M, Rivas R, Garcia-Fraile P (2018) Discovery of phloeophagus beetles as a source of pseudomonas strains that produce potentially new bioactive substances and description of pseudomonas bohemica sp. nov. Front Microbiol 9:913. https://doi.org/10.3389/fmicb.2018.00913

    Article  PubMed  Google Scholar 

  12. Yoshino Y, Kitazawa T, Kamimura M, Tatsuno K, Ota Y, Yotsuyanagi H (2011) Pseudomonas putida bacteremia in adult patients: five case reports and a review of the literature. J Infect Chemother 17(2):278–282. https://doi.org/10.1007/s10156-010-0114-0

    Article  PubMed  Google Scholar 

  13. Parte AC (2018) LPSN—list of prokaryotic names with standing in nomenclature (bacterio.net), 20 years on. Int J Syst Evol Microbiol 68(6):1825–1829. https://doi.org/10.1099/ijsem.0.002786

    Article  PubMed  Google Scholar 

  14. Parte AC (2014) LPSN–list of prokaryotic names with standing in nomenclature. Nucleic Acids Res 42(Database issue):D613–D616. https://doi.org/10.1093/nar/gkt1111

    Article  CAS  PubMed  Google Scholar 

  15. Gomila M, Pena A, Mulet M, Lalucat J, Garcia-Valdes E (2015) Phylogenomics and systematics in Pseudomonas. Front Microbiol 6:214. https://doi.org/10.3389/fmicb.2015.00214

    Article  PubMed  PubMed Central  Google Scholar 

  16. Mulet M, Lalucat J, Garcia-Valdes E (2010) DNA sequence-based analysis of the Pseudomonas species. Environ Microbiol 12(6):1513–1530. https://doi.org/10.1111/j.1462-2920.2010.02181.x

    Article  CAS  PubMed  Google Scholar 

  17. Poblete-Castro I, Becker J, Dohnt K, dos Santos VM, Wittmann C (2012) Industrial biotechnology of Pseudomonas putida and related species. Appl Microbiol Biotechnol 93(6):2279–2290. https://doi.org/10.1007/s00253-012-3928-0

    Article  CAS  PubMed  Google Scholar 

  18. Puchalka J, Oberhardt MA, Godinho M, Bielecka A, Regenhardt D, Timmis KN, Papin JA, Martins dos Santos VA (2008) Genome-scale reconstruction and analysis of the Pseudomonas putida KT2440 metabolic network facilitates applications in biotechnology. PLoS Comput Biol 4(10):e1000210. https://doi.org/10.1371/journal.pcbi.1000210

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Gao J, Xie G, Peng F, Xie Z (2015) Pseudomonas donghuensis sp. nov., exhibiting high-yields of siderophore. Antonie Van Leeuwenhoek 107(1):83–94. https://doi.org/10.1007/s10482-014-0306-1

    Article  CAS  PubMed  Google Scholar 

  20. Wittgens A, Santiago-Schuebel B, Henkel M, Tiso T, Blank LM, Hausmann R, Hofmann D, Wilhelm S, Jaeger KE, Rosenau F (2018) Heterologous production of long-chain rhamnolipids from Burkholderia glumae in Pseudomonas putida-a step forward to tailor-made rhamnolipids. Appl Microbiol Biotechnol 102(3):1229–1239. https://doi.org/10.1007/s00253-017-8702-x

    Article  CAS  PubMed  Google Scholar 

  21. Wang J, Ma W, Wang Y, Lin L, Wang T, Wang Y, Li Y, Wang X (2018) Deletion of 76 genes relevant to flagella and pili formation to facilitate polyhydroxyalkanoate production in Pseudomonas putida. Appl Microbiol Biotechnol 102(24):10523–10539. https://doi.org/10.1007/s00253-018-9439-x

    Article  CAS  PubMed  Google Scholar 

  22. Mindt M, Walter T, Risse JM, Wendisch VF (2018) Fermentative production of N-methylglutamate from glycerol by recombinant Pseudomonas putida. Front Bioeng Biotechnol 6:159. https://doi.org/10.3389/fbioe.2018.00159

    Article  PubMed  PubMed Central  Google Scholar 

  23. Kurzbaum E, Raizner Y, Cohen O, Suckeveriene RY, Kulikov A, Hakimi B, Iasur Kruh L, Armon R, Farber Y, Menashe O (2017) Encapsulated Pseudomonas putida for phenol biodegradation: use of a structural membrane for construction of a well-organized confined particle. Water Res 121:37–45. https://doi.org/10.1016/j.watres.2017.04.079

    Article  CAS  PubMed  Google Scholar 

  24. Mulet M, Sanchez D, Lalucat J, Lee K, Garcia-Valdes E (2015) Pseudomonas alkylphenolica sp nov, a bacterial species able to form special aerial structures when grown on p-cresol. Int J Syst Evol Microbiol 65(11):4013–4018. https://doi.org/10.1099/ijsem.0.000529

    Article  CAS  PubMed  Google Scholar 

  25. Chen Q, Tu H, Luo X, Zhang B, Huang F, Li Z, Wang J, Shen W, Wu J, Cui Z (2016) The regulation of para-nitrophenol degradation in Pseudomonas putida DLL-E4. PLoS ONE 11(5):e0155485. https://doi.org/10.1371/journal.pone.0155485

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Yang L, Cai T, Ding D, Cai T, Jiang C, Li H, Yang Q, Chen L (2017) Biodegradation of 2-hydroxyl-1,4 naphthoquinone (lawsone) by Pseudomonas taiwanensis LH-3 isolated from activated sludge. Sci Rep 7(1):6795. https://doi.org/10.1038/s41598-017-06338-1

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Cabral L, Yu RQ, Crane S, Giovanella P, Barkay T, Camargo FA (2016) Methylmercury degradation by Pseudomonas putida V1. Ecotoxicol Environ Saf 130:37–42. https://doi.org/10.1016/j.ecoenv.2016.03.036

    Article  CAS  PubMed  Google Scholar 

  28. Jackman SD, Vandervalk BP, Mohamadi H, Chu J, Yeo S, Hammond SA, Jahesh G, Khan H, Coombe L, Warren RL, Birol I (2017) ABySS 2.0: resource-efficient assembly of large genomes using a Bloom filter. Genome Res 27(5):768–777. https://doi.org/10.1101/gr.214346.116

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. 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(14):6614–6624. https://doi.org/10.1093/nar/gkw569

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Yoon SH, Ha SM, Kwon S, Lim J, Kim Y, Seo H, Chun J (2017) Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int J Syst Evol Microbiol 67(5):1613–1617. https://doi.org/10.1099/ijsem.0.001755

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Kumar S, Stecher G, Li M, Knyaz C, Tamura K (2018) MEGA X: molecular Evolutionary Genetics Analysis across Computing Platforms. Mol Biol Evol 35(6):1547–1549. https://doi.org/10.1093/molbev/msy096

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4(4):406–425. https://doi.org/10.1093/oxfordjournals.molbev.a040454

    Article  CAS  PubMed  Google Scholar 

  33. Tamura K, Nei M (1993) Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol 10(3):512–526. https://doi.org/10.1093/oxfordjournals.molbev.a040023

    Article  CAS  PubMed  Google Scholar 

  34. Fitch WM (1971) Toward defining the course of evolution: minimum change for a specific tree topology. Syst Zool 20(4):406–416. https://doi.org/10.2307/2412116

    Article  Google Scholar 

  35. Felsenstein J (1985) Confidence limits on phylogenies: an approach using the bootstrap. Evolution 39(4):783–791. https://doi.org/10.1111/j.1558-5646.1985.tb00420.x

    Article  PubMed  Google Scholar 

  36. Chun J, Oren A, Ventosa A, Christensen H, Arahal DR, da Costa MS, Rooney AP, Yi H, Xu XW, De Meyer S, Trujillo ME (2018) Proposed minimal standards for the use of genome data for the taxonomy of prokaryotes. Int J Syst Evol Microbiol 68(1):461–466. https://doi.org/10.1099/ijsem.0.002516

    Article  PubMed  Google Scholar 

  37. Richter M, Rossello-Mora R (2009) Shifting the genomic gold standard for the prokaryotic species definition. Proc Natl Acad Sci USA 106(45):19126–19131. https://doi.org/10.1073/pnas.0906412106

    Article  PubMed  PubMed Central  Google Scholar 

  38. Lee I, Ouk Kim Y, Park SC, Chun J (2016) OrthoANI: an improved algorithm and software for calculating average nucleotide identity. Int J Syst Evol Microbiol 66(2):1100–1103. https://doi.org/10.1099/ijsem.0.000760

    Article  CAS  PubMed  Google Scholar 

  39. Yoon SH, Ha SM, Lim J, Kwon S, Chun J (2017) A large-scale evaluation of algorithms to calculate average nucleotide identity. Antonie Van Leeuwenhoek 110(10):1281–1286. https://doi.org/10.1007/s10482-017-0844-4

    Article  CAS  PubMed  Google Scholar 

  40. Meier-Kolthoff JP, Auch AF, Klenk HP, Goker M (2013) Genome sequence-based species delimitation with confidence intervals and improved distance functions. BMC Bioinformatics 14:60. https://doi.org/10.1186/1471-2105-14-60

    Article  PubMed  PubMed Central  Google Scholar 

  41. Mulet M, Gomila M, Scotta C, Sanchez D, Lalucat J, Garcia-Valdes E (2012) Concordance between whole-cell matrix-assisted laser-desorption/ionization time-of-flight mass spectrometry and multilocus sequence analysis approaches in species discrimination within the genus Pseudomonas. Syst Appl Microbiol 35(7):455–464. https://doi.org/10.1016/j.syapm.2012.08.007

    Article  CAS  PubMed  Google Scholar 

  42. Frasson D, Opoku M, Picozzi T, Torossi T, Balada S, Smits THM, Hilber U (2017) Pseudomonas wadenswilerensis sp. nov. and Pseudomonas reidholzensis sp. nov., two novel species within the Pseudomonas putida group isolated from forest soil. Int J Syst Evol Microbiol 67(8):2853–2861. https://doi.org/10.1099/ijsem.0.002035

    Article  CAS  PubMed  Google Scholar 

  43. Rutz D, Frasson D, Sievers M, Blom J, Rezzonico F, Pothier JF, Smits THM (2018) High-quality draft genome sequence of Pseudomonas wadenswilerensis CCOS 864(T). Microbiol Resour Announc 7(16):e01059. https://doi.org/10.1128/mra.01059-18

    Article  PubMed  PubMed Central  Google Scholar 

  44. Gao J, Li BY, Wang HH, Liu ZQ (2014) Pseudomonas hunanensis sp nov, isolated from soil subjected to long-term manganese pollution. Curr Microbiol 69(1):19–24. https://doi.org/10.1007/s00284-014-0545-4

    Article  CAS  PubMed  Google Scholar 

  45. Meier-Kolthoff JP, Klenk HP, Goker M (2014) Taxonomic use of DNA G + C content and DNA-DNA hybridization in the genomic age. Int J Syst Evol Microbiol 64(Pt 2):352–356. https://doi.org/10.1099/ijs.0.056994-0

    Article  CAS  PubMed  Google Scholar 

  46. Rossello-Mora R, Amann R (2001) The species concept for prokaryotes. FEMS Microbiol Rev 25(1):39–67. https://doi.org/10.1111/j.1574-6976.2001.tb00571.x

    Article  CAS  PubMed  Google Scholar 

  47. Garibaldi JA (1967) Media for the enhancement of fluorescent pigment production by Pseudomonas species. J Bacteriol 94(5):1296–1299

    CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

This work was supported by a grant from the Qingmiao Project of Hubei University of Chinese Medicine (Grant No. 5112-0007). We thank Dr Zong Qi and Dr Wang Fangkui for their assistance in Biolog GENIII tests.

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Xiang, W., Chen, S., Tian, D. et al. Pseudomonas hutmensis sp. nov., a New Fluorescent Member of Pseudomonas putida Group. Curr Microbiol 76, 872–878 (2019). https://doi.org/10.1007/s00284-019-01701-z

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