| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Cindy H. Nakatsu | Q113960814 |
| P2093 | author name string | Yoichi Kamagata | |
| Kozo Asano | |||
| Michiko Tanaka | |||
| Indun Dewi Puspita | |||
| P2860 | cites work | Instability and decay of the primary structure of DNA | Q22122361 |
| Microbial community analysis of soils contaminated with lead, chromium and petroleum hydrocarbons | Q46931721 | ||
| Bacterial activity, community structure, and centimeter-scale spatial heterogeneity in contaminated soil | Q46931723 | ||
| A novel approach for high throughput cultivation assays and the isolation of planktonic bacteria | Q47799028 | ||
| Culture-dependent and independent analyses of the microbial communities inhabiting the giant duckweed (Spirodela polyrrhiza) rhizoplane and isolation of a variety of rarely cultivated organisms within the phylum Verrucomicrobia | Q48066512 | ||
| Viability, diversity and composition of the bacterial community in a high Arctic permafrost soil from Spitsbergen, Northern Norway | Q48077111 | ||
| Role of catalase and oxyR in the viable but nonculturable state of Vibrio vulnificus | Q48166264 | ||
| Cyclic adenosine monophosphate in bacteria | Q50240174 | ||
| Dormant forms of Mycobacterium smegmatis with distinct morphology. | Q50613807 | ||
| Bacterial resuscitation factors: revival of viable but non-culturable bacteria. | Q51125463 | ||
| Microbial seed banks: the ecological and evolutionary implications of dormancy. | Q51173560 | ||
| Cell-to-cell communication in the populations of enterobacterium Erwinia carotovora ssp. atroseptica SCRI1043 during adaptation to stress conditions. | Q51629055 | ||
| Formation and resuscitation of "non-culturable" cells of Rhodococcus rhodochrous and Mycobacterium tuberculosis in prolonged stationary phase. | Q51718626 | ||
| Role of lipid components in formation and reactivation of Mycobacterium smegmatis "nonculturable" cells. | Q53243196 | ||
| Ultrastructure of coccoid viable but non-culturable Vibrio cholerae. | Q53577511 | ||
| Modification of the peptidoglycan of Escherichia coli in the viable but nonculturable state. | Q54551655 | ||
| Stimulation of the multiplication of Micrococcus luteus by an autocrine growth factor | Q56974749 | ||
| On resuscitation from the dormant state of Micrococcus luteus. | Q56974797 | ||
| Exit from dormancy in microbial organisms | Q57153699 | ||
| Microbial awakenings | Q59064494 | ||
| Characterization of Bacterial Communities from Activated Sludge: Culture-Dependent Numerical Identification Versus In Situ Identification Using Group- and Genus-Specific rRNA-Targeted Oligonucleotide Probes | Q71210457 | ||
| Morphology of the viable but nonculturable Vibrio cholerae as determined by the freeze fixation technique | Q72877732 | ||
| Resuscitation of viable but nonculturable cells of Vibrio parahaemolyticus induced at low temperature under starvation | Q73708983 | ||
| Evidence of autoinducer activity in naturally occurring biofilms | Q73733390 | ||
| A comparison of solid and liquid media for resuscitation of starvation- and low-temperature-induced nonculturable cells of Aeromonas hydrophila | Q73803787 | ||
| [Reproductive resting forms of Arthrobacter globiformis] | Q74093018 | ||
| Viable but non-culturable and dormant bacteria: time to resolve an oxymoron and a misnomer? | Q74342872 | ||
| Resuscitation rate in different enterococcal species in the viable but non-culturable state | Q77652519 | ||
| Restoration of culturability of starvation-stressed and low-temperature-stressed Escherichia coli O157 cells by using H2O2-degrading compounds | Q77978505 | ||
| Gene expression profile of Vibrio cholerae in the cold stress-induced viable but non-culturable state | Q79946965 | ||
| [The role of intercellular contacts in the initiation of growth and in the development of a transiently nonculturable state by the cultures of Rhodococcus rhodochrous grown in poor media] | Q81324840 | ||
| Resuscitation of Vibrio vulnificus from the Viable but Nonculturable State | Q82817069 | ||
| Dormant ovoid cells of Mycobacterium tuberculosis are formed in response to gradual external acidification | Q83286782 | ||
| Chemical characterization of soil extract as growth media for the ecophysiological study of bacteria | Q83522980 | ||
| A six-well plate method: less laborious and effective method for cultivation of obligate anaerobic microorganisms | Q84391523 | ||
| [Dormant form of Micrococcus luteus and Arthrobacter globiformis, not growing on standard media] | Q84720593 | ||
| Survival and viability of nonculturableEscherichia coli andVibrio cholerae in the estuarine and marine environment | Q86719054 | ||
| Robert Koch and the ‘golden age’ of bacteriology | Q22252186 | ||
| The Uncultured Microbial Majority | Q22255617 | ||
| Quorum Sensing in Bacteria | Q22255618 | ||
| Impact of culture-independent studies on the emerging phylogenetic view of bacterial diversity. | Q24521497 | ||
| Phylogenetic identification and in situ detection of individual microbial cells without cultivation | Q24651527 | ||
| A bacterial cytokine | Q24678303 | ||
| The peptidoglycan of stationary-phase Mycobacterium tuberculosis predominantly contains cross-links generated by L,D-transpeptidation | Q28486366 | ||
| A member of the cAMP receptor protein family of transcription regulators in Mycobacterium tuberculosis is required for virulence in mice and controls transcription of the rpfA gene coding for a resuscitation promoting factor | Q28487026 | ||
| Resuscitation of dormant Mycobacterium tuberculosis by phospholipids or specific peptides | Q28487096 | ||
| A eukaryotic-like Ser/Thr kinase signals bacteria to exit dormancy in response to peptidoglycan fragments | Q28488857 | ||
| Quorum sensing: cell-to-cell communication in bacteria | Q29547325 | ||
| Cultivation of globally distributed soil bacteria from phylogenetic lineages previously only detected in cultivation-independent surveys | Q30750881 | ||
| Spatial and resource factors influencing high microbial diversity in soil | Q30790282 | ||
| High-throughput methods for culturing microorganisms in very-low-nutrient media yield diverse new marine isolates | Q30839805 | ||
| Culturability and In situ abundance of pelagic bacteria from the North Sea | Q30883516 | ||
| Laboratory cultivation of widespread and previously uncultured soil bacteria | Q30885664 | ||
| Cultivation-dependent and -independent approaches for determining bacterial diversity in heavy-metal-contaminated soil | Q30943901 | ||
| Quorum sensing in Pseudomonas aeruginosa controls expression of catalase and superoxide dismutase genes and mediates biofilm susceptibility to hydrogen peroxide | Q33179293 | ||
| Comparative analysis of bacterial diversity in freshwater sediment of a shallow eutrophic lake by molecular and improved cultivation-based techniques | Q33213774 | ||
| Culturability and coexistence of colony-forming and single-cell marine bacterioplankton | Q33221278 | ||
| Structural characterization of Salmonella typhimurium YeaZ, an M22 O-sialoglycoprotein endopeptidase homolog | Q33240038 | ||
| Short peptide induces an "uncultivable" microorganism to grow in vitro | Q33339256 | ||
| Differentially expressed genes in Mycobacterium tuberculosis H37Rv under mild acidic and hypoxic conditions | Q33385423 | ||
| Fluorescence polarization in studies of bacterial cytoplasmic membrane fluidity under environmental stress | Q33437669 | ||
| Microbial community analysis in the roots of aquatic plants and isolation of novel microbes including an organism of the candidate phylum OP10. | Q33674812 | ||
| Identification of cyclic AMP-regulated genes in Mycobacterium tuberculosis complex bacteria under low-oxygen conditions | Q33726844 | ||
| Vertical distribution of bacteria in a lake sediment from Antarctica by culture-independent and culture-dependent approaches | Q33761922 | ||
| Bacterial dormancy and culturability: the role of autocrine growth factors | Q33941499 | ||
| The extracytoplasmic domain of the Mycobacterium tuberculosis Ser/Thr kinase PknB binds specific muropeptides and is required for PknB localization | Q33987461 | ||
| Recent findings on the viable but nonculturable state in pathogenic bacteria | Q34020799 | ||
| Cyclic AMP and acyl homoserine lactones increase the cultivation efficiency of heterotrophic bacteria from the central Baltic Sea. | Q34056603 | ||
| Specific detection, isolation, and characterization of selected, previously uncultured members of the freshwater bacterioplankton community | Q34097766 | ||
| Isolating "uncultivable" microorganisms in pure culture in a simulated natural environment | Q34127944 | ||
| Hierarchical Evolution of the Bacterial Sporulation Network | Q34149232 | ||
| Development of 16S rRNA-gene-targeted group-specific primers for the detection and identification of predominant bacteria in human feces | Q34165676 | ||
| Survival strategies of bacteria in the natural environment. | Q34173787 | ||
| Measurement of in situ activities of nonphotosynthetic microorganisms in aquatic and terrestrial habitats | Q34194521 | ||
| Microcolony cultivation on a soil substrate membrane system selects for previously uncultured soil bacteria | Q34232157 | ||
| Soil microbial community responses to additions of organic carbon substrates and heavy metals (Pb and Cr). | Q34232817 | ||
| Regulation of endospore formation in Bacillus subtilis | Q34307580 | ||
| Responses of the anaerobic bacterial community to addition of organic C in chromium(VI)- and iron(III)-amended microcosms | Q34316188 | ||
| Cultivating the uncultured | Q34388876 | ||
| Total counts of marine bacteria include a large fraction of non-nucleoid-containing bacteria (ghosts). | Q34422735 | ||
| Cell density-regulated recovery of starved biofilm populations of ammonia-oxidizing bacteria | Q34427844 | ||
| Small talk. Cell-to-cell communication in bacteria. | Q34710012 | ||
| Effect of signal compounds and incubation conditions on the culturability of freshwater bacterioplankton | Q34993392 | ||
| Human colonic biota studied by ribosomal DNA sequence analysis. | Q35191757 | ||
| Bacterial diversity among small-subunit rRNA gene clones and cellular isolates from the same seawater sample | Q35198559 | ||
| Cyclic AMP in prokaryotes | Q35227904 | ||
| Seasonal incidence of Vibrio vulnificus in the Great Bay estuary of New Hampshire and Maine | Q35694022 | ||
| Life after log | Q36109652 | ||
| Long-term survival during stationary phase: evolution and the GASP phenotype | Q36369839 | ||
| Bacterially speaking | Q36456225 | ||
| Wake up! Peptidoglycan lysis and bacterial non-growth states. | Q36468473 | ||
| Phospholipid ester-linked fatty acid profile changes during nutrient deprivation of Vibrio cholerae: increases in the trans/cis ratio and proportions of cyclopropyl fatty acids | Q36667613 | ||
| Uptake of Cyclic AMP by Natural Populations of Marine Bacteria. | Q36707884 | ||
| I will survive: DNA protection in bacterial spores | Q36750425 | ||
| Structure, assembly, and function of the spore surface layers. | Q37012825 | ||
| New strategies for cultivation and detection of previously uncultured microbes | Q37044291 | ||
| Turnover of cell walls in microorganisms | Q37064802 | ||
| How bacteria consume their own exoskeletons (turnover and recycling of cell wall peptidoglycan) | Q37183911 | ||
| Resuscitation-promoting factors as lytic enzymes for bacterial growth and signaling | Q37607321 | ||
| Bacterial competition: surviving and thriving in the microbial jungle | Q37641019 | ||
| Strategies for culture of 'unculturable' bacteria | Q37757054 | ||
| Uncultured microorganisms as a source of secondary metabolites | Q37774548 | ||
| Ecological and evolutionary interactions in syntrophic methanogenic consortia | Q37876065 | ||
| A great leap forward in microbial ecology. | Q37876069 | ||
| The myriad roles of cyclic AMP in microbial pathogens: from signal to sword | Q37955761 | ||
| Bacterial growth stimulation with exogenous siderophore and synthetic N-acyl homoserine lactone autoinducers under iron-limited and low-nutrient conditions | Q39486095 | ||
| Cell wall chemical composition of Enterococcus faecalis in the viable but nonculturable state | Q39536230 | ||
| Mycobacterial stationary phase induced by low oxygen tension: cell wall thickening and localization of the 16-kilodalton alpha-crystallin homolog. | Q39564571 | ||
| Improved culturability of soil bacteria and isolation in pure culture of novel members of the divisions Acidobacteria, Actinobacteria, Proteobacteria, and Verrucomicrobia. | Q39653368 | ||
| Quantitative fluorescence in situ hybridization of Bifidobacterium spp. with genus-specific 16S rRNA-targeted probes and its application in fecal samples. | Q39798215 | ||
| In situ analysis of nucleic acids in cold-induced nonculturable Vibrio vulnificus | Q39802551 | ||
| Probing activated sludge with oligonucleotides specific for proteobacteria: inadequacy of culture-dependent methods for describing microbial community structure | Q39857519 | ||
| Dormancy in Stationary-Phase Cultures of Micrococcus luteus: Flow Cytometric Analysis of Starvation and Resuscitation | Q39858872 | ||
| Influence of Viable Cells on the Resuscitation of Dormant Cells in Micrococcus luteus Cultures Held in an Extended Stationary Phase: the Population Effect. | Q39916029 | ||
| Changes in Ester-Linked Phospholipid Fatty Acid Profiles of Subsurface Bacteria during Starvation and Desiccation in a Porous Medium. | Q39916033 | ||
| Membrane fatty acid and virulence changes in the viable but nonculturable state of Vibrio vulnificus | Q39922020 | ||
| Entry of Vibrio cincinnatiensis into viable but nonculturable state and its resuscitation | Q40004884 | ||
| Incubation of environmental samples in a diffusion chamber increases the diversity of recovered isolates | Q40006482 | ||
| Effects of growth medium, inoculum size, and incubation time on culturability and isolation of soil bacteria | Q40985942 | ||
| Siderophores from neighboring organisms promote the growth of uncultured bacteria | Q41846710 | ||
| Unique roles of DosT and DosS in DosR regulon induction and Mycobacterium tuberculosis dormancy | Q41872000 | ||
| Hollow-fiber membrane chamber as a device for in situ environmental cultivation | Q42121166 | ||
| Separation by dielectrophoresis of dormant and nondormant bacterial cells of Mycobacterium smegmatis | Q42122944 | ||
| Resuscitation of the viable but non-culturable state of Salmonella enterica serovar Oranienburg by recombinant resuscitation-promoting factor derived from Salmonella Typhimurium strain LT2. | Q42670161 | ||
| Biochemical and morphological changes in dormant ("Nonculturable") Mycobacterium smegmatis cells | Q43121005 | ||
| Occurrence and degradation of peptidoglycan in aquatic environments. | Q43283180 | ||
| Factors influencing the cultivability of lake water bacteria | Q43744155 | ||
| Mycolic acid structure determines the fluidity of the mycobacterial cell wall | Q44732618 | ||
| Formation of 'non-culturable' cells of Mycobacterium smegmatis in stationary phase in response to growth under suboptimal conditions and their Rpf-mediated resuscitation. | Q44927291 | ||
| Biochemical and virulence characterization of viable but nonculturable cells of Vibrio parahaemolyticus | Q45155991 | ||
| Effect of recombinant Rv1009 protein on promoting the growth of Mycobacterium tuberculosis | Q45342937 | ||
| Muralytic activity of Micrococcus luteus Rpf and its relationship to physiological activity in promoting bacterial growth and resuscitation | Q46854868 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 4 | |
| P921 | main subject | bacteria | Q10876 |
| physiological phenomenon | Q66615932 | ||
| P304 | page(s) | 356-366 | |
| P577 | publication date | 2012-10-10 | |
| P1433 | published in | Microbes and environments / JSME | Q26867035 |
| P1476 | title | Are uncultivated bacteria really uncultivable? | |
| P478 | volume | 27 |
| Q39631247 | A Synthetic Ecology Perspective: How Well Does Behavior of Model Organisms in the Laboratory Predict Microbial Activities in Natural Habitats? |
| Q34595561 | A hidden pitfall in the preparation of agar media undermines microorganism cultivability |
| Q34147200 | A survey on cultivable heterotrophic bacteria inhabiting a thermally unstratified water column in an Atlantic Rainforest lake. |
| Q99633749 | An approach to increase the success rate of cultivation of soil bacteria based on fluorescence-activated cell sorting |
| Q24619768 | As-yet-uncultivated oral bacteria: breadth and association with oral and extra-oral diseases |
| Q35602413 | Bacterial and fungal communities in a degraded ombrotrophic peatland undergoing natural and managed re-vegetation |
| Q26780417 | Bioluminescence assay for cell viability |
| Q33805662 | Cultivating yet-to-be cultivated microbes: the challenge continues |
| Q55370241 | Different Metabolomic Responses to Carbon Starvation between Light and Dark Conditions in the Purple Photosynthetic Bacterium, Rhodopseudomonas palustris. |
| Q41955022 | Draft Genome Sequence of Tomitella biformata AHU 1821T, Isolated from a Permafrost Ice Wedge in Alaska |
| Q33697510 | Ecological perspectives on microbes involved in N-cycling |
| Q35640340 | Effect of Probiotics/Prebiotics on Cattle Health and Productivity |
| Q57071056 | Emergent Properties of Microbial Activity in Heterogeneous Soil Microenvironments: Different Research Approaches Are Slowly Converging, Yet Major Challenges Remain |
| Q28080553 | Emerging concepts promising new horizons for marine biodiscovery and synthetic biology |
| Q92461166 | High proportions of bacteria and archaea across most biomes remain uncultured |
| Q35134168 | Identification and characterization of carboxyl esterases of gill chamber-associated microbiota in the deep-sea shrimp Rimicaris exoculata by using functional metagenomics |
| Q89489603 | Improved Isolation of Uncultured Anaerobic Bacteria using Medium Prepared with Separate Sterilization of Agar and Phosphate |
| Q35717714 | Increase in Bacterial Colony Formation from a Permafrost Ice Wedge Dosed with a Tomitella biformata Recombinant Resuscitation-Promoting Factor Protein. |
| Q26775404 | Individuality, phenotypic differentiation, dormancy and 'persistence' in culturable bacterial systems: commonalities shared by environmental, laboratory, and clinical microbiology |
| Q36095755 | Innovative Approaches Using Lichen Enriched Media to Improve Isolation and Culturability of Lichen Associated Bacteria |
| Q99572022 | Integration of absolute multi-omics reveals dynamic protein-to-RNA ratios and metabolic interplay within mixed-domain microbiomes |
| Q35060166 | Is the improvement of CF patients, hospitalized for pulmonary exacerbation, correlated to a decrease in bacterial load? |
| Q90374098 | Isolation of Previously Uncultured Slow-Growing Bacteria by Using a Simple Modification in the Preparation of Agar Media |
| Q35407852 | Isolation of a significant fraction of non-phototroph diversity from a desert Biological Soil Crust |
| Q35569594 | Isolation of microorganisms involved in reduction of crystalline iron(III) oxides in natural environments |
| Q36365313 | Keys to Cultivating Uncultured Microbes: Elaborate Enrichment Strategies and Resuscitation of Dormant Cells |
| Q38791327 | Low abundant soil bacteria can be metabolically versatile and fast growing |
| Q35743668 | Metabarcoding of the kombucha microbial community grown in different microenvironments |
| Q36068973 | Metagenomics and Bioinformatics in Microbial Ecology: Current Status and Beyond. |
| Q37016497 | Microbes in the Water Infrastructure: Underpinning Our Society |
| Q64102460 | Microbial Metabolism and Community Dynamics in Hydraulic Fracturing Fluids Recovered From Deep Hydrocarbon-Rich Shale |
| Q39014923 | Microbial resource utilization traits and trade-offs: implications for community structure, functioning, and biogeochemical impacts at present and in the future |
| Q90376461 | Model Microbial Consortia as Tools for Understanding Complex Microbial Communities |
| Q89547443 | Molecular assays to detect the presence and viability of Phytophthora ramorum and Grosmannia clavigera |
| Q92134295 | Novel bioactive natural products from bacteria via bioprospecting, genome mining and metabolic engineering |
| Q47778092 | Phosphate-Catalyzed Hydrogen Peroxide Formation from Agar, Gellan, and κ-Carrageenan and Recovery of Microbial Cultivability via Catalase and Pyruvate |
| Q27695721 | Pressure adaptation is linked to thermal adaptation in salt-saturated marine habitats |
| Q33806713 | Rediscovery of the microbial world in microbial ecology |
| Q33805728 | Resuscitation promoting factor (Rpf) from Tomitella biformata AHU 1821(T) promotes growth and resuscitates non-dividing cells. |
| Q35809539 | Shedding light on microbial dark matter: a TM6 bacterium as natural endosymbiont of a free-living amoeba |
| Q34672144 | The challenges of studying the anaerobic microbial world |
| Q33920202 | The combination of functional metagenomics and an oil-fed enrichment strategy revealed the phylogenetic diversity of lipolytic bacteria overlooked by the cultivation-based method. |
| Q34474989 | The dormant blood microbiome in chronic, inflammatory diseases |
| Q30224335 | The multi-omics promise in context: from sequence to microbial isolate |
| Q29616595 | The rebirth of culture in microbiology through the example of culturomics to study human gut microbiota |
| Q90705131 | Thermoanaerosceptrum fracticalcis gen. nov. sp. nov., a Novel Fumarate-Fermenting Microorganism From a Deep Fractured Carbonate Aquifer of the US Great Basin |
| Q28601184 | Wake me when it's over - Bacterial toxin-antitoxin proteins and induced dormancy |
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