Pseudomonas

Palleroni, Norberto J.

doi:10.1002/9781118960608.gbm01210

Cited by 85Bacterial Genetics and BiotechnologyGenomics and Phylogenetic StudiesBacterial biofilms and quorum sensing

Pseudomonas

Palleroni, Norberto J.·2015·Bergey's Manual of Systematics of Archaea and Bacteria

DOI 10.1002/9781118960608.gbm01210

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Abstract

Abstract Pseu.do'mo.nas or Pseu.do.mo'nas. Gr. adj. pseudes false; Gr. n. monas a unit, monad; M.L. fem. n. Pseudomonas false monad. Straight or slightly curved rods but not helical, 0.5–1.0 × 1.5–5.0 µm. Most of the species do not accumulate granules of polyhydroxybutyrate , but accumulation of polyhydroxyalkanoates of monomer lengths higher than C 4 may occur when growing on alkanes or gluconate. Do not produce prosthecae and are not surrounded by sheaths. No resting stages are known. Gram negative. Motile by one or several polar flagella ; rarely nonmotile. In some species lateral flagella of short wavelength may also be formed. Aerobic, having a strictly respiratory type of metabolism with oxygen as the terminal electron acceptor; in some cases nitrate can be used as an alternate electron acceptor , allowing growth to occur anaerobically. Xanthomonadins are not produced . Most, if not all, species fail to grow under acid conditions (pH 4.5 or lower). Most species do not require organic growth factors. Oxidase positive or negative. Catalase positive. Chemoorganotrophic. Strains of the species include in their composition the hydroxylated fatty acids C 10 : 0 3OH and C 12 : 0 , and C 12 : 0 2OH , and ubiquinone Q‐9 . Widely distributed in nature. Some species are pathogenic for humans, animals, or plants. The mol % G + C of the DNA is : 58–69. Type species : Pseudomonas aeruginosa (Schroeter 1872) Migula 1900, 884 ( Bacterium aeruginosum Schroeter 1872, 126.) Taxonomic and Nomenclature Notes According to the List of Prokaryotic names with Standing in Nomenclature (LPSN), the taxonomic status of the genus Pseudomonas is: correct name (last update, February 2025) * . LPSN classification: Bacteria / Pseudomonadati / Pseudomonadota / Gammaproteobacteria / Pseudomonadales / Pseudomonadaceae / Pseudomonas The genus Pseudomonas can also be recovered in the Genome Taxonomy Database (GTDB) as g__Pseudomonas (version v220) ** . GTDB classification: d__Bacteria / p__Pseudomonadota / c__Gammaproteobacteria / o__Pseudomonadales / f__Pseudomonadaceae / g__Pseudomonas * Meier‐Kolthoff et al. ( 2022 ). Nucleic Acids Res , 50 , D801 – D807 ; DOI: 10.1093/nar/gkab902 ** Parks

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Pseudomonas, Acinetobacter and Labrenzia are genera found in marine environments.
“Bacterial communities specifically associated with the egg samples (Fig. 5B) were dominated by Pseudomonas, Acinetobacter and Labrenzia, 3 genera found in marine environments (Fournier & Richet, 2006; Palleroni, 2015; Raj Sharma et al., 2019) and which had already been studied during the development of L. vannamei and P. monodon (Rungrassamee et al., 2013; Wang et al., 2020a; Wang et al., 2020b).”
From Potential lineage transmission within the active microbiota of the eggs and the nauplii of the shrimp Litopenaeus stylirostris : possible influence of the rearing water and more (2021) · cites this paper as Palleroni, 2015
Pseudomonas and Corynebacterium are able to degrade different organic carbon sources using extracellular enzymes.
“Like Alteromonas and Vibrios, Pseudomonas and Corynebacterium are able to degrade different organic carbon sources using extracellular enzymes and could thus find optimal growth conditions with shrimp eggs and the nauplii explaining why they were so abundant among these samples (Palleroni, 2015; Tsuzukibashi et al., 2017).”
From Potential lineage transmission within the active microbiota of the eggs and the nauplii of the shrimp Litopenaeus stylirostris : possible influence of the rearing water and more (2021) · cites this paper as Palleroni, 2015
Pseudomonas and Corynebacterium could find optimal growth conditions with shrimp eggs and the nauplii, explaining why they were so abundant among these samples.
“Like Alteromonas and Vibrios, Pseudomonas and Corynebacterium are able to degrade different organic carbon sources using extracellular enzymes and could thus find optimal growth conditions with shrimp eggs and the nauplii explaining why they were so abundant among these samples (Palleroni, 2015; Tsuzukibashi et al., 2017).”
From Potential lineage transmission within the active microbiota of the eggs and the nauplii of the shrimp Litopenaeus stylirostris : possible influence of the rearing water and more (2021) · cites this paper as Palleroni, 2015

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Ferric uptake regulator mutants of Pseudomonas aeruginosa with distinct alterations in the iron‐dependent repression of exotoxin A and siderophores in aerobic and microaerobic environments
Barton, H. A., Johnson, Z., Cox, C. D., Vasil, A. I., & Vasil, M. L. (1996) · Molecular Microbiology · doi:10.1046/j.1365-2958.1996.381426.x · Cited by 113 · see citing works
Changing Concepts in Host-Pathogen Genetics
Ellingboe, A. H. (1981) · Annual Review of Phytopathology · doi:10.1146/annurev.py.19.090181.001013 · Cited by 113 · see citing works
NAH plasmid-mediated catabolism of anthracene and phenanthrene to naphthoic acids
Menn, F.-M., Applegate, B. M., & Sayler, G. S. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.6.1938-1942.1993 · Cited by 112 · see citing works
Possible regulatory role for nonaromatic carbon sources in styrene degradation by Pseudomonas putida CA-3
O’Connor, K. E., Buckley, C. M., Hartmans, S., & Dobson, A. D. W. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.2.544-548.1995 · Cited by 112 · see citing works
Nutritional and biochemical comparisons of plant-pathogenic and saprophytic fluorescent pseudomonads.
Misaghi, I. J., & Rg, G. (1969) · PubMed · Cited by 111 · see citing works
STUDIES IN BACTERIOSIS II1.: A BROWN BLOTCH DISEASE OF CULTIVATED MUSHROOMS.
Paine, S. G. (1919) · Annals of Applied Biology · doi:10.1111/j.1744-7348.1919.tb05291.x · Cited by 109 · see citing works
Comparative typing of Pseudomonas aeruginosa by random amplification of polymorphic DNA or pulsed-field gel electrophoresis of DNA macrorestriction fragments
Renders, N. H. M., Römling, U., Verbrugh, H. A., & van Belkum, A. (1996) · Journal of Clinical Microbiology · doi:10.1128/jcm.34.12.3190-3195.1996 · Cited by 109 · see citing works
Pectate and Pectin Gels for Differentiation of Pseudomonas sp. and Other Bacterial Plant Pathogens
Hildebrand, D. C. (1971) · Phytopathology · doi:10.1094/phyto-61-1430 · Cited by 108 · see citing works
Cloning of the genes for and characterization of the early stages of toluene and o-xylene catabolism in Pseudomonas stutzeri OX1
Bertoni, G., Bolognese, F., Galli, E., & Barbieri, P. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.10.3704-3711.1996 · Cited by 108 · see citing works
16S rRNA Gene Sequence Analysis Relative to Genomovars of Pseudomonas stutzeri and Proposal of Pseudomonas balearica sp. nov.
Bennasar-Figueras, A., Rossello-Mora, R. A., Lalucat, J., & Moore, E. R. B. (1996) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-46-1-200 · Cited by 108 · see citing works
Pseudomonas monteilii sp. nov., Isolated from Clinical Specimens
Elomari, M., Coroler, L., Verhille, S., Izard, D., & Leclerc, H. (1997) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-47-3-846 · Cited by 106 · see citing works
Classification of the spoilage flora offish, with special reference to Shewanella putrefaciens
Stenström, I., & Molin, G. (1990) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1990.tb05226.x · Cited by 105 · see citing works
Two New Species of Pseudomonas: P. oryzihabitans Isolated from Rice Paddy and Clinical Specimens and P. luteola Isolated from Clinical Specimens
KODAMA, K., KIMURA, N., & Komagata, K. (1985) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-35-4-467 · Cited by 104 · see citing works
Analysis of the Pseudomonas aeruginosa elastase (lasB) regulatory region
Rust, L., Pesci, E. C., & Iglewski, B. H. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.4.1134-1140.1996 · Cited by 103 · see citing works
Nonpathogenic Members of the Genus Pseudomonas
Stolp, H., & Gadkari, D. (1981) · Springer eBooks · doi:10.1007/978-3-662-13187-9_61 · Cited by 102 · see citing works
Construction of an MR/P fimbrial mutant of Proteus mirabilis: role in virulence in a mouse model of ascending urinary tract infection
Bahrani, F. K., Massad, G., Lockatell, C. V., Johnson, D. E., Russell, R. G., Warren, J. W., & Mobley, H. L. T. (1994) · Infection and Immunity · doi:10.1128/iai.62.8.3363-3371.1994 · Cited by 101 · see citing works
Tomato pith necrosis caused by Pseudomonas corrugata n. sp.
SCARLETT, C. M., FLETCHER, J. T., Roberts, P., & Lelliott, R. A. (1978) · Annals of Applied Biology · doi:10.1111/j.1744-7348.1978.tb00684.x · Cited by 101 · see citing works
Augmentation of oxidant injury to human pulmonary epithelial cells by the Pseudomonas aeruginosa siderophore pyochelin
Britigan, B. E., Rasmussen, G. T., & Cox, C. D. (1997) · Infection and Immunity · doi:10.1128/iai.65.3.1071-1076.1997 · Cited by 101 · see citing works
Formation and function of Vibrio parahaemolyticus lateral flagella
Shinoda, S., & Okamoto, K. (1977) · Journal of Bacteriology · doi:10.1128/jb.129.3.1266-1271.1977 · Cited by 101 · see citing works
Biochemical Identification of Citrobacter Species Defined by DNA Hybridization and Description of Citrobacter gillenii sp. nov. (Formerly Citrobacter Genomospecies 10) and Citrobacter murliniae sp. nov. (Formerly Citrobacter Genomospecies 11)
Brenner, D. J., O'Hara, C. M., Grimont, P. A. D., Janda, J. M., Falsen, E., Aldova, E., Ageron, E., Schindler, J., Abbott, S. L., & Steigerwalt, A. G. (1999) · Journal of Clinical Microbiology · doi:10.1128/jcm.37.8.2619-2624.1999 · Cited by 100 · see citing works
Halovibrio variabilis gen. nov. sp. nov., Pseudomonas halophila sp. nov. and a New Halophilic Aerobic Coccoid Eubacterium from Great Salt Lake, Utah, USA
Fendrich, C. (1988) · Systematic and Applied Microbiology · doi:10.1016/s0723-2020(88)80046-8 · Cited by 100 · see citing works
Degradation of methyl parathion by Pseudomonas putida
Rani, N. L., & Lalithakumari, D. (1994) · Canadian Journal of Microbiology · doi:10.1139/m94-160 · Cited by 99 · see citing works
Role of PyoverdinePf, the Iron-binding Fluorescent Pigment of Pseudomonas fluorescens, in Iron Transport
Meyer, J., & Hornsperger, J. (1978) · Journal of General Microbiology · doi:10.1099/00221287-107-2-329 · Cited by 99 · see citing works
The Bacterial Flora of Distilled and Stored Water. III. new species of the genera Corynebacterium, Flavobacterium, Spirillum and Pseudomonas
Leifson, E. (1962) · International Journal of Systematic Bacteriology · doi:10.1099/0096266x-12-4-161 · Cited by 98 · see citing works

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A critical review of bioleaching of rare earth elements: The mechanisms and effect of process parameters
Rasoulnia, P., Barthen, R., & Lakaniemi, A. (2020) · Critical Reviews in Environmental Science and Technology · doi:10.1080/10643389.2020.1727718 · Cited by 241 · see citing works
Fermented fish and fermented fish-based products, an ever-growing source of microbial diversity: A literature review
Belleggia, L., & Osimani, A. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113112 · Cited by 111 · see citing works
Antibiotic Resistant Pseudomonas Spp. Spoilers in Fresh Dairy Products: An Underestimated Risk and the Control Strategies
Quintieri, L., Fanelli, F., & Caputo, L. (2019) · Foods · doi:10.3390/foods8090372 · Cited by 104 · see citing works
Harnessing Pseudomonas spp. for sustainable plant crop protection
Alattas, H., Glick, B. R., Murphy, D. V., & Scott, C. S. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1485197 · Cited by 102 · see citing works
Dynamic microbial diversity and fermentation quality of the mixed silage of corn and soybean grown in strip intercropping system
Zeng, T., Li, X., Guan, H., Yang, W., Liu, W., Liu, J., Du, Z., Li, X., Xiao, Q., Wang, X., et al. (2020) · Bioresource Technology · doi:10.1016/j.biortech.2020.123655 · Cited by 92 · see citing works
Microbial biopreservatives for controlling the spoilage of beef and lamb meat: their application and effects on meat quality
Xu, M. M., Kaur, M., Pillidge, C. J., & Torley, P. J. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1877108 · Cited by 64 · see citing works
Antagonistic Potential of Fluorescent Pseudomonads Colonizing Wheat Heads Against Mycotoxin Producing Alternaria and Fusaria
Müller, T., Ruppel, S., Behrendt, U., Lentzsch, P., & Müller, M. E. H. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02124 · Cited by 48 · see citing works
Long-Term Survival of Synechococcus and Heterotrophic Bacteria without External Nutrient Supply after Changes in Their Relationship from Antagonism to Mutualism
Zhang, Z., Nair, S., Tang, L., Zhao, H., Hu, Z., Chen, M., Zhang, Y., Kao, S., Jiao, N., & Zhang, Y. (2021) · mBio · doi:10.1128/mbio.01614-21 · Cited by 48 · see citing works
Phylogenomics studies and molecular markers reliably demarcate genus Pseudomonas sensu stricto and twelve other Pseudomonadaceae species clades representing novel and emended genera
Rudra, B., & Gupta, R. S. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1273665 · Cited by 49 · see citing works
Comparative Genomics and Evolutionary Analysis of RNA-Binding Proteins of the CsrA Family in the Genus Pseudomonas
Sobrero, P. M., & Valverde, C. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00127 · Cited by 43 · see citing works
Culture-Independent Survey of Thermophilic Microbial Communities of the North Caucasus
Toshchakov, S. V., Izotova, A. O., Vinogradova, E. N., Созырович, К. Г., Tuaeva, A. Y., Abaev, V. T., Evteeva, M. A., Gunitseva, N. M., Korzhenkov, A. A., Elcheninov, A. G., et al. (2021) · Biology · doi:10.3390/biology10121352 · Cited by 36 · see citing works
Emerging microbiota during cold storage and temperature abuse of ready-to-eat salad
Söderqvist, K., Osman, O. A., Wolff, C., Bertilsson, S., Vågsholm, I., & Boqvist, S. (2017) · Infection Ecology & Epidemiology · doi:10.1080/20008686.2017.1328963 · Cited by 36 · see citing works
Bacterial degradation of bisphenol analogues: an overview
Farias, J. D. M., & Krepsky, N. (2022) · Environmental Science and Pollution Research · doi:10.1007/s11356-022-23035-3 · Cited by 35 · see citing works
Molecular Characterization and Taxonomic Assignment of Three Phage Isolates from a Collection Infecting Pseudomonas syringae pv. actinidiae and P. syringae pv. phaseolicola from Northern Italy
Martino, G., Holtappels, D., Vallino, M., Chiapello, M., Turina, M., Lavigne, R., Wagemans, J., & Ciuffo, M. (2021) · Viruses · doi:10.3390/v13102083 · Cited by 31 · see citing works
Isolation of Hermetia illucens larvae core gut microbiota by two different cultivation strategies
Cifuentes, Y., Vilcinskas, A., Kämpfer, P., & Glaeser, S. P. (2022) · Antonie van Leeuwenhoek · doi:10.1007/s10482-022-01735-7 · Cited by 34 · see citing works
Extraction and purification of pyocyanin: a simpler and more reliable method
Nawas, T. (2018) · MOJ Toxicology · doi:10.15406/mojt.2018.04.00139 · Cited by 28 · see citing works
Pseudomonas laurylsulfatovorans sp. nov., sodium dodecyl sulfate degrading bacteria, isolated from the peaty soil of a wastewater treatment plant
Furmanczyk, E. M., Kaminski, M. A., Lipiński, L., Dziembowski, A., & Sobczak, A. J. (2018) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2018.03.009 · Cited by 28 · see citing works
Adaptation of Microbial Communities to Environmental Arsenic and Selection of Arsenite-Oxidizing Bacteria From Contaminated Groundwaters
Zecchin, S., Crognale, S., Zaccheo, P., Fazi, S., Amalfitano, S., Casentini, B., Callegari, M., Zanchi, R., Sacchi, G. A., Rossetti, S., et al. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.634025 · Cited by 24 · see citing works
The DEAD-box RNA helicase RhlE2 is a global regulator of Pseudomonas aeruginosa lifestyle and pathogenesis
Hausmann, S., González, D., Geiser, J., & Valentini, M. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab503 · Cited by 24 · see citing works
Development of an Autochthonous Microbial Consortium for Enhanced Bioremediation of PAH-Contaminated Soil
Roszak, M., Jabłońska, J., Stachurska, X., Dubrowska, K., Kajdanowicz, J., Gołębiewska, M., Kiepas-Kokot, A., Osińska, B., Augustyniak, A., & Karakulska, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413469 · Cited by 24 · see citing works
Potential lineage transmission within the active microbiota of the eggs and the nauplii of the shrimp Litopenaeus stylirostris : possible influence of the rearing water and more
Giraud, C., Callac, N., Beauvais, M., Mailliez, J.-R., Ansquer, D., Selmaoui-Folcher, N., Pham, D., Wabete, N., & Boulo, V. (2021) · PeerJ · doi:10.7717/peerj.12241 · Cited by 23 · see citing works
Architectural Features and Resistance to Food-Grade Disinfectants in Listeria monocytogenes-Pseudomonas spp. Dual-Species Biofilms
Rodríguez-López, P., Rodríguez-Herrera, J. J., & Cabo, M. L. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.917964 · Cited by 18 · see citing works
The phenotypic and genetic characteristics of Pseudomonas anguilliseptica strains associated with mortalities in farmed sea bream and sea bass
Tawfeek, W. S., Kassab, A. S., Okasha, L. A., Abdelsalam, M., & Sherif, A. H. (2023) · Aquaculture International · doi:10.1007/s10499-023-01360-9 · Cited by 17 · see citing works
Microbiome Composition and Borrelia Detection in Ixodes scapularis Ticks at the Northwestern Edge of Their Range
Sperling, J. L. H., Fitzgerald, D. T., Sperling, F. A. H., & Magor, K. E. (2020) · Tropical Medicine and Infectious Disease · doi:10.3390/tropicalmed5040173 · Cited by 17 · see citing works
The challenge of removing waste from wastewater: let technology use nature!
Nunes, O. C. (2020) · Microbial Biotechnology · doi:10.1111/1751-7915.13711 · Cited by 14 · see citing works
Mentholation triggers brand-specific shifts in the bacterial microbiota of commercial cigarette products
Malayil, L., Chattopadhyay, S., Kulkarni, P., Hittle, L. E., Clark, P. I., Mongodin, E. F., & Sapkota, A. R. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10681-1 · Cited by 14 · see citing works
Temperature- and Nutrients-Induced Phenotypic Changes of Antarctic Green Snow Bacteria Probed by High-Throughput FTIR Spectroscopy
Smirnova, M., Tafintseva, V., Köhler, A., Miamin, U., & Shapaval, V. (2022) · Biology · doi:10.3390/biology11060890 · Cited by 14 · see citing works
The effect of urbanization on planktonic and biofilm bacterial communities in different water bodies of the Danube River in Hungary
Lennert, K. J., Borsodi, A. K., Anda, D., Krett, G., Kós, P. B., & Engloner, A. I. (2024) · Scientific Reports · doi:10.1038/s41598-024-75863-7 · Cited by 13 · see citing works
Identification of enriched hyperthermophilic microbial communities from a deep-sea hydrothermal vent chimney under electrolithoautotrophic culture conditions
Pillot, G., Ali, O. A., Davidson, S., Shintu, L., Godfroy, A., Combet-Blanc, Y., Bonin, P., & Liebgott, P.-P. (2021) · Scientific Reports · doi:10.1038/s41598-021-94135-2 · Cited by 12 · see citing works
Taxonomic description and draft genome of Pseudomonas sediminis sp. nov., isolated from the rhizospheric sediment of Phragmites karka
Behera, P., Mahapatra, M., Seuylemezian, A., Vaishampayan, P., Ramana, V. V., Joseph, N., Joshi, A. A., Shouche, Y. S., Suar, M., Pattnaik, A. K., et al. (2018) · The Journal of Microbiology · doi:10.1007/s12275-018-7549-x · Cited by 12 · see citing works
Pseudomonas sichuanensis sp. nov., isolated from hospital sewage
Qin, J., Hu, Y., Feng, Y., Lü, X., & Zong, Z. (2018) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijsem.0.003188 · Cited by 12 · see citing works
Standard Microbiological Techniques (Staining, Morphological and Cultural Characteristics, Biochemical Properties, and Serotyping) in the Detection of ESKAPE Pathogens
Parasuraman, P., Busi, S., & Lee, J.-K. (2024) · Springer eBooks · doi:10.1007/978-981-99-8799-3_4 · Cited by 12 · see citing works
Absence of oxygen effect on microbial structure and methane production during drying and rewetting events
Liu, T., Li, X., Yekta, S. S., Björn, A. V., Mu, B., Masuda, L. S. M., Schnürer, A., & Enrich‐Prast, A. (2022) · Scientific Reports · doi:10.1038/s41598-022-20448-5 · Cited by 10 · see citing works
A comparative evaluation of freezing criteria and molecular characterization of epiphytic ice-nucleating (Ice+) and non-ice-nucleating (Ice−) Pseudomonas syringae and Pseudomonas fluorescens
Karimi, B., Nosrati, R., Bazzaz, B. S. F., Mirpour, M., Malboobi, M., & Owlia, P. (2019) · Journal of Plant Pathology · doi:10.1007/s42161-019-00402-7 · Cited by 10 · see citing works
Screening of Endophytic Bacteria as Biocontrol Agents Against Bacteria Leaf Blight (Xanthomonas oryzae)
Halim, R. A., Hasan, N., & Ramachandran, K. (2020) · HAYATI Journal of Biosciences · doi:10.4308/hjb.27.3.215 · Cited by 10 · see citing works
Mild hydrostatic-pressure (15 MPa) affects the assembly, but not the growth, of oil-degrading coastal microbial communities tested under limiting conditions (5°C, no added nutrients)
Barbato, M., & Scoma, A. (2020) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiaa160 · Cited by 9 · see citing works
Challenges in Studying the Incorporation of Nanomaterials to Building Materials on Microbiological Models
Augustyniak, A., Sikora, P., Cendrowski, K., Nawrotek, P., Mijowska, E., & Stephan, D. A. (2019) · Springer proceedings in physics · doi:10.1007/978-3-030-17755-3_20 · Cited by 9 · see citing works
Exploring the microbiota of tomato and strawberry plants as sources of bio-protective cultures for fruits and vegetables preservation
Rabasco-Vílchez, L., Bolívar, A., Martín, R. M., & Pérez‐Rodríguez, F. (2024) · Future Foods · doi:10.1016/j.fufo.2024.100344 · Cited by 8 · see citing works
Involvement of the MxtR/ErdR (CrbS/CrbR) Two-Component System in Acetate Metabolism in Pseudomonas putida KT2440
Henríquez, T., & Jung, H. (2021) · Microorganisms · doi:10.3390/microorganisms9081558 · Cited by 8 · see citing works
Taxonomic identification and diversity of effective soil microorganisms: towards a better understanding of this microbiome
Carabeo-Pérez, A., Jiménez, J., Unday, Z. G., Henderson, D., Adams, P., & Hurtado, A. C. (2022) · Agronomía Colombiana · doi:10.15446/agron.colomb.v40n2.101378 · Cited by 8 · see citing works
Biohydrogen production from wastewater-grown microalgae-bacteria consortia: Optimizing inoculum selection for enhanced yield
Silva, T. A., de Araújo, M. N., de Rezende, E. G. F., Saia, F. T., Magalhães, I. B., Pereira, A. S. A. D. P., Ferreira, J., Gregoracci, G. B., Adorno, M. Â. T., Fuess, L. T., et al. (2025) · Renewable Energy · doi:10.1016/j.renene.2025.123079 · Cited by 8 · see citing works
Phosphorus and ammonium removal characteristics from aqueous solutions by a newly isolated plant growth-promoting bacterium
Daly, I., Jellali, S., Mehri, I., Reis, M. A. M., Freitas, E. B., Oehmen, A., & Chatti, A. (2019) · Environmental Technology · doi:10.1080/09593330.2019.1575917 · Cited by 8 · see citing works
Pyocin‐mediated antagonistic interactions in Pseudomonas spp. isolated in James Ross Island, Antarctica
Snopková, K., Dufková, K., Chamrád, I., Lenobel, R., Čejková, D., Kosina, M., Hrala, M., Holá, V., Sedláček, I., & Šmajs, D. (2021) · Environmental Microbiology · doi:10.1111/1462-2920.15809 · Cited by 7 · see citing works
Involvement of MexS and MexEF-OprN in Resistance to Toxic Ion Chelators in Pseudomonas putida KT2440
Henríquez, T., Baldow, T., Lo, Y. K., Weydert, D., Brachmann, A., & Jung, H. (2020) · Microorganisms · doi:10.3390/microorganisms8111782 · Cited by 7 · see citing works
Description of Pseudomonas imrae sp. nov., carrying a novel class C β-lactamase gene variant, isolated from gut samples of Atlantic mackerel (Scomber scombrus)
Salvà‐Serra, F., Nimje, P. S., Piñeiro-Iglesias, B., Alarcón, L. A., Cardew, S., Inganäs, E., Jensie-Markopoulos, S., Ohlén, M., Sailer, H.-S., Unosson, C., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1530878 · Cited by 6 · see citing works
The Influence of Hydrodynamic Conditions in a Laboratory-Scale Bioreactor on Pseudomonas aeruginosa Metabolite Production
Konopacki, M., Jabłońska, J., Dubrowska, K., Augustyniak, A., Grygorcewicz, B., Gliźniewicz, M., Wróblewski, E., Kordas, M., Dołęgowska, B., & Rakoczy, R. (2022) · Microorganisms · doi:10.3390/microorganisms11010088 · Cited by 6 · see citing works
Agriculturally Important Microbes: Challenges and Opportunities
Joshi, P., Saini, A., Banerjee, S., Bose, R., Bhandari, M. S., Pandey, A., & Pandey, S. (2021) · Springer eBooks · doi:10.1007/978-981-16-2922-8_1 · Cited by 7 · see citing works
Biofilm development on fractured rock in oligotrophic nitrate-rich groundwater: An in-situ bioreactor study
Park, K.-H., Kim, K., Kirk, M. F., & Kwon, M. J. (2025) · Water Research · doi:10.1016/j.watres.2025.123329 · Cited by 5 · see citing works
High-Quality Draft Genome Sequence of Pseudomonas wadenswilerensis CCOS 864 T
Rutz, D., Frasson, D., Sievers, M., Blom, J., Rezzonico, F., Pothier, J. F., & Smits, T. H. M. (2018) · Microbiology Resource Announcements · doi:10.1128/mra.01059-18 · Cited by 5 · see citing works
Analysis of the utility of a rapid vesicle isolation method for clinical strains of Pseudomonas aeruginosa
Henríquez, T., Santoro, F., Medaglini, D., Pallecchi, L., Clemente, I., Bonechi, C., Magnani, A., Paccagnini, E., Gentile, M., Lupetti, P., et al. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.00649-24 · Cited by 5 · see citing works
Molecular Markers Specific for the Pseudomonadaceae Genera Provide Novel and Reliable Means for the Identification of Other Pseudomonas Strains/spp. Related to These Genera
Rudra, B., & Gupta, R. S. (2025) · Genes · doi:10.3390/genes16020183 · Cited by 5 · see citing works
Characterization and optimization of biogenic copper nanoparticles synthesized by Pseudomonas putida with cytocompatibility investigation
El-Sayed, O., Abd-Elhalim, B. T., Mohamed, M. A., & Hassan, E. (2025) · Scientific Reports · doi:10.1038/s41598-025-17705-8 · Cited by 4 · see citing works
What’s in the Pipeline? Evidence on the Transmission of SARS-CoV-2 via Building Wastewater Plumbing Systems
Dight, T., & Gormley, M. J. (2021) · Frontiers in Built Environment · doi:10.3389/fbuil.2021.641745 · Cited by 4 · see citing works
Pseudomonas spirodelae, sp. nov., a bacterium isolated from the roots of the aquatic plant Spirodela polyrhiza
Vandeborne, K., Guy, N., Lengyel, G. A., Franks, J. M., & Maltman, C. (2025) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijsem.0.006637 · Cited by 3 · see citing works
Identification of bacterial communities associated with needle mushroom (Flammulina filiformis) and its production environment
Liu, Z., Cong, Y., Sossah, F. L., Sheng, H., & Li, Y. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1429213 · Cited by 3 · see citing works
Continuum modeling of bioclogging of soil aquifer treatment systems segregating active and inactive biomass
Cifuentes, E. S., Furman, A., Rosenzweig, R., & Packman, A. I. (2025) · Hydrology and earth system sciences · doi:10.5194/hess-29-6999-2025 · Cited by 3 · see citing works
Enantioselective desymmetrization strategy of prochiral 1,3-diols in natural product synthesis
Wei, L., Yang, R., Shi, Z., & Ma, Z. (2025) · Beilstein Journal of Organic Chemistry · doi:10.3762/bjoc.21.151 · Cited by 2 · see citing works
Fatty Liver Disease and Bacterial Co-Infection in Cultured Marine Fish
Duman, M., Altun, S., Ozdemir, B., & Satıcıoğlu, İ. B. (2022) · Erciyes Üniversitesi Veteriner Fakültesi Dergisi · doi:10.32707/ercivet.1085205 · Cited by 2 · see citing works
Serial cultures in invert emulsion and monophase systems for microbial community shaping and propagation
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Authors: Palleroni, N. J.
Affiliations: Rutgers, The State University of New Jersey (US)
Corresponding author: Palleroni, Norberto J.
Venue: Bergey's Manual of Systematics of Archaea and Bacteria
Publisher: Wiley
Published: 2015-09-14
Pages: 1-1
DOI: 10.1002/9781118960608.gbm01210
OpenAlex: W4211084001
Cited by: 85
References: 555
Citations by year: 2026: 5 · 2025: 13 · 2024: 10 · 2023: 4 · 2022: 8 · 2021: 19 · 2020: 12 · 2019: 6 · 2018: 7 · 2017: 1
Type: other
Language: en
Open access: closed
Licence: doi.wiley.com/10.1002/tdm_license_1.1 (tdm)
Locations: Bergey's Manual of Systematics of Archaea and Bacteria (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
Keywords: Pseudomonas, bacterial taxonomy, bacterial nomenclature, Pseudomonas aeruginosa, polyhydroxyalkanoates, polyhydroxybutyrate, bacterial morphology, Gram-negative bacteria, hydroxy fatty acids, pathogenic bacteria, Gammaproteobacteria, Pseudomonadaceae

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