Cited by 1,059Bacterial biofilms and quorum sensingBacterial Genetics and BiotechnologyEscherichia coli research studies

The DOI matches its Crossref record; 177 of the 177 references it cites were found in a registry or an index.

Indole as an intercellular signal in microbial communities

Open access

Lee, Jin-Hyung, Lee, Jintae·2010·FEMS Microbiology Reviews

DOI 10.1111/j.1574-6976.2009.00204.x

Open this paper in CoChat — free account Open PDF

Abstract

Bacteria can utilize signal molecules to coordinate their behavior to survive in dynamic multispecies communities. Indole is widespread in the natural environment, as a variety of both Gram-positive and Gram-negative bacteria (to date, 85 species) produce large quantities of indole. Although it has been known for over 100 years that many bacteria produce indole, the real biological roles of this molecule are only now beginning to be unveiled. As an intercellular signal molecule, indole controls diverse aspects of bacterial physiology, such as spore formation, plasmid stability, drug resistance, biofilm formation, and virulence in indole-producing bacteria. In contrast, many non-indole-producing bacteria, plants and animals produce diverse oxygenases which may interfere with indole signaling. It appears indole plays an important role in bacterial physiology, ecological balance, and possibly human health. Here we discuss our current knowledge and perspectives on indole signaling.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1111/j.1574-6976.2009.00204.x

Cites

177 of 177 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

QUORUM SENSING: Cell-to-Cell Communication in Bacteria
Waters, C. M., & Bassler, B. L. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.012704.131001 · Cited by 3,989
Quorum sensing in bacteria: the LuxR-LuxI family of cell density-responsive transcriptional regulators
Fuqua, W. C., Winans, S. C., & Greenberg, E. P. (1994) · Journal of Bacteriology · doi:10.1128/jb.176.2.269-275.1994 · Cited by 2,941
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677
Commensal Host-Bacterial Relationships in the Gut
Hooper, L. V., & Gordon, J. I. (2001) · Science · doi:10.1126/science.1058709 · Cited by 2,362
Attenuation of Pseudomonas aeruginosa virulence by quorum sensing inhibitors
Hentzer, M., Wu, H., Andersen, J. B., Riedel, K., Rasmussen, T. B., Bagge, N., Kumar, N., Schembri, M. A., Song, Z., Kristoffersen, P., et al. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg366 · Cited by 1,440
Microbes in Gastrointestinal Health and Disease
Neish, A. S. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.10.080 · Cited by 1,423
Identification, Timing, and Signal Specificity of Pseudomonas aeruginosa Quorum-Controlled Genes: a Transcriptome Analysis
Schuster, M., Lostroh, P., Ogi, T., & Greenberg, E. P. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.7.2066-2079.2003 · Cited by 1,127
Inhibition of quorum sensing in Pseudomonas aeruginosa biofilm bacteria by a halogenated furanone compound
Hentzer, M., Riedel, K., Rasmussen, T. B., Heydorn, A., Andersen, J. B., Parsek, M. R., Rice, S. A., Eberl, L., Molin, S., Høiby, N., et al. (2002) · Microbiology · doi:10.1099/00221287-148-1-87 · Cited by 1,053
How bacteria talk to each other: regulation of gene expression by quorum sensing
Bassler, B. L. (1999) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(99)00025-9 · Cited by 1,046
Cruciferous vegetables and human cancer risk: epidemiologic evidence and mechanistic basis
Higdon, J. V., Delage, B., WILLIAMS, D., & Dashwood, R. H. (2007) · Pharmacological Research · doi:10.1016/j.phrs.2007.01.009 · Cited by 1,038
Quorum sensing controls biofilm formation in Vibrio cholerae
Hammer, B. K., & Bassler, B. L. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03688.x · Cited by 888
The bacterial signal indole increases epithelial-cell tight-junction resistance and attenuates indicators of inflammation
Bansal, T., Alaniz, R. C., Wood, T. K., & Jayaraman, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906112107 · Cited by 868
Look who's talking: communication and quorum sensing in the bacterial world
Williams, P., Winzer, K., Chan, W., & Cámara, M. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2039 · Cited by 834
Communication in bacteria: an ecological and evolutionary perspective
Keller, L., & Surette, M. G. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1383 · Cited by 826
Cooperation and conflict in quorum-sensing bacterial populations
Diggle, S. P., Griffin, A. S., Campbell, G. S., & West, S. A. (2007) · Nature · doi:10.1038/nature06279 · Cited by 824
Quorum sensing and environmental adaptation in Pseudomonas aeruginosa: a tale of regulatory networks and multifunctional signal molecules
Williams, P. M., & Cámara, M. (2009) · Current Opinion in Microbiology · doi:10.1016/j.mib.2009.01.005 · Cited by 797
The biology and future prospects of antivirulence therapies
Cegelski, L., Marshall, G. R., Eldridge, G. R., & Hultgren, S. J. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1818 · Cited by 788
Classification, Identification, and Clinical Significance of Proteus , Providencia , and Morganella
O'Hara, C. M., Brenner, F. W., & Miller, J. M. (2000) · Clinical Microbiology Reviews · doi:10.1128/cmr.13.4.534-546.2000 · Cited by 766
Inter-kingdom signalling: Communication between bacteria and their hosts
Hughes, D. T., & Sperandio, V. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1836 · Cited by 761
LuxS quorum sensing: more than just a numbers game
Xavier, K. B., & Bassler, B. L. (2003) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(03)00028-6 · Cited by 750
Quorum-sensing inhibitors as anti-pathogenic drugs
Rasmussen, T. B., & Givskov, M. (2006) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2006.02.005 · Cited by 737
A Taxonomic Study of the Genus Haemophilus, with the Proposal of a New Species
Kilian, M. (1976) · Journal of General Microbiology · doi:10.1099/00221287-93-1-9 · Cited by 721
Making 'sense' of metabolism: autoinducer-2, LUXS and pathogenic bacteria
Vendeville, A., Winzer, K., Heurlier, K., Tang, C. M., & Hardie, K. R. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1146 · Cited by 674
Quorum sensing in Escherichia coli and Salmonella typhimurium
Surette, M. G., & Bassler, B. L. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.7046 · Cited by 642
Expression of Naphthalene Oxidation Genes in Escherichia coli Results in the Biosynthesis of Indigo
Ensley, B. D., Ratzkin, B. J., Osslund, T. D., Simon, M. J., Wackett, L. P., & Gibson, D. T. (1983) · Science · doi:10.1126/science.6353574 · Cited by 563
Autoinducer 2 Controls Biofilm Formation in Escherichia coli through a Novel Motility Quorum-Sensing Regulator (MqsR, B3022)
Barrios, A. F. G., Zuo, R., Hashimoto, Y., Li, Y., Bentley, W. E., & Wood, T. K. (2005) · Journal of Bacteriology · doi:10.1128/jb.188.1.305-316.2006 · Cited by 545
Indole is an inter-species biofilm signal mediated by SdiA
Lee, J., Jayaraman, A., & Wood, T. K. (2007) · BMC Microbiology · doi:10.1186/1471-2180-7-42 · Cited by 471
Regulation of Uptake and Processing of the Quorum-Sensing Autoinducer AI-2 in Escherichia coli
Xavier, K. B., & Bassler, B. L. (2004) · Journal of Bacteriology · doi:10.1128/jb.187.1.238-248.2005 · Cited by 440
Salinibacter ruber gen. nov., sp. nov., a novel, extremely halophilic member of the Bacteria from saltern crystallizer ponds.
Antón, J., Oren, A., Benlloch, S., Rodríguez‐Valera, F., Amann, R., & Rossello-Mora, R. A. (2002) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-52-2-485 · Cited by 440
Oxalobacter formigenes gen. nov., sp. nov.: oxalate-degrading anaerobes that inhabit the gastrointestinal tract
Allison, M. J., Dawson, K. A., Mayberry, W. R., & Foss, J. G. (1985) · Archives of Microbiology · doi:10.1007/bf00446731 · Cited by 437
Potent Neuroprotective Properties against the Alzheimer β-Amyloid by an Endogenous Melatonin-related Indole Structure, Indole-3-propionic Acid
Chyan, Y., Pöeggeler, B., Omar, R., Chain, D. G., Frangione, B., Ghiso, J. A., & Pappolla, M. A. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.31.21937 · Cited by 409
The Evolution of Quorum Sensing in Bacterial Biofilms
Nadell, C. D., Xavier, J. B., Levin, S. A., & Foster, K. R. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060014 · Cited by 407
The end products of the metabolism of aromatic amino acids by Clostridia
Elsden, S. R., Hilton, M. G., & Waller, J. M. (1976) · Archives of Microbiology · doi:10.1007/bf00425340 · Cited by 396
Quorum-quenching microbial infections: mechanisms and implications
Dong, Y.-H., Wang, L., & Zhang, L. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2045 · Cited by 380
Transfer of Enterobacter agglomerans (Beijerinck 1888) Ewing and Fife 1972 to Pantoea gen. nov. as Pantoea agglomerans comb. nov. and Description of Pantoea dispersa sp. nov.
Gavini, F., Mergaert, J., BEJI, A., Mielcarek, C., Izard, D., Kersters, K., & Ley, J. D. (1989) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-39-3-337 · Cited by 375
Autoinducer 2: a concentration‐dependent signal for mutualistic bacterial biofilm growth
Rickard, A. H., Palmer, R. J., Jr., Blehert, D. S., Campagna, S. R., Semmelhack, M. F., Egland, P. G., Bassler, B. L., & Kolenbrander, P. E. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05202.x · Cited by 366
Differential Effects of Epinephrine, Norepinephrine, and Indole on Escherichia coli O157:H7 Chemotaxis, Colonization, and Gene Expression
Bansal, T., Englert, D. L., Lee, J., Hegde, M., Wood, T. K., & Jayaraman, A. (2007) · Infection and Immunity · doi:10.1128/iai.00630-07 · Cited by 358
Bacterial Quorum Sensing: Signals, Circuits, and Implications for Biofilms and Disease
Jayaraman, A., & Wood, T. K. (2008) · Annual Review of Biomedical Engineering · doi:10.1146/annurev.bioeng.10.061807.160536 · Cited by 350
Bacterial cell-to-cell communication: sorry, can't talk now — gone to lunch!
Winzer, K. (2002) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(02)00304-1 · Cited by 346
Cell‐to‐cell signalling in Escherichia coli and Salmonella enterica
Ahmer, B. M. M. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04054.x · Cited by 329
Indole induces the expression of multidrug exporter genes in Escherichia coli
Hirakawa, H., Inazumi, Y., Masaki, T., Hirata, T., & Yamaguchi, A. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04449.x · Cited by 328
Interference with AI-2-mediated bacterial cell–cell communication
Xavier, K. B., & Bassler, B. L. (2005) · Nature · doi:10.1038/nature03960 · Cited by 322
Oxidation of Indole by Cytochrome P450 Enzymes
Gillam, E. M. J., Notley, L. M., Cai, H., De Voss, J. J., & Guengerich, F. P. (2000) · Biochemistry · doi:10.1021/bi001229u · Cited by 313
Quorum sensing and signal interference: diverse implications
Zhang, L., & Dong, Y. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04234.x · Cited by 312
Diffusible signals and interspecies communication in bacteria
Ryan, R. P., & Dow, J. M. (2008) · Microbiology · doi:10.1099/mic.0.2008/017871-0 · Cited by 298
Vibrio vulnificus biogroup 2: new biogroup pathogenic for eels
Tison, D. L., Nishibuchi, M., Greenwood, J. D., & Seidler, R. J. (1982) · Applied and Environmental Microbiology · doi:10.1128/aem.44.3.640-646.1982 · Cited by 290
Evolutionary theory of bacterial quorum sensing: when is a signal not a signal?
Diggle, S. P., Gardner, A., West, S. A., & Griffin, A. S. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2049 · Cited by 270
The Vibrio harveyi quorum-sensing system uses shared regulatory components to discriminate between multiple autoinducersPreprint
Waters, C. M., & Bassler, B. L. (2006) · Genes & Development · doi:10.1101/gad.1466506 · Cited by 261
Indole Can Act as an Extracellular Signal in Escherichia coli
Wang, D., Ding, X., & Rather, P. N. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.14.4210-4216.2001 · Cited by 256
Indole can act as an extracellular signal to regulate biofilm formation ofEscherichia coliand other indole-producing bacteria
Martino, P. D., Fursy, R., Bret, L., Sundararaju, B., & Phillips, R. S. (2003) · Canadian Journal of Microbiology · doi:10.1139/w03-056 · Cited by 255
Indole and 7‐hydroxyindole diminish Pseudomonas aeruginosa virulence
Lee, J., Attila, C., Cirillo, S. L. G., Cirillo, J. D., & Wood, T. K. (2008) · Microbial Biotechnology · doi:10.1111/j.1751-7915.2008.00061.x · Cited by 244
YliH (BssR) and YceP (BssS) Regulate Escherichia coli K-12 Biofilm Formation by Influencing Cell Signaling
Domka, J., Lee, J., & Wood, T. K. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.4.2449-2459.2006 · Cited by 244
YcfR (BhsA) InfluencesEscherichia coliBiofilm Formation through Stress Response and Surface Hydrophobicity
Zhang, X., García‐Contreras, R., & Wood, T. K. (2007) · Journal of Bacteriology · doi:10.1128/jb.01832-06 · Cited by 234
Regulation of LuxPQ Receptor Activity by the Quorum-Sensing Signal Autoinducer-2
Neiditch, M. B., Federle, M. J., Miller, S. T., Bassler, B. L., & Hughson, F. M. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.04.020 · Cited by 232
Escherichia albertii sp. nov., a diarrhoeagenic species isolated from stool specimens of Bangladeshi children
Huys, G. R. B., Cnockaert, M. C., Janda, J. M., & Swings, J. (2003) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.02475-0 · Cited by 228
Acid- and Base-Induced Proteins during Aerobic and Anaerobic Growth of Escherichia coli Revealed by Two-Dimensional Gel Electrophoresis
Blankenhorn, D., Phillips, J., & Slonczewski, J. L. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.7.2209-2216.1999 · Cited by 225
The phn Genes of Burkholderia sp. Strain RP007 Constitute a Divergent Gene Cluster for Polycyclic Aromatic Hydrocarbon Catabolism
Laurie, A. D., & Lloyd-Jones, G. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.2.531-540.1999 · Cited by 224
Interkingdom signaling: Deciphering the language of acyl homoserine lactones
Shiner, E. K., Rumbaugh, K. P., & Williams, S. C. (2005) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2005.03.001 · Cited by 222
Establishing bacterial communities by 'word of mouth': LuxS and autoinducer 2 in biofilm development
Hardie, K. R., & Heurlier, K. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1916 · Cited by 222
Classification of Desulfovibrio species, the nonsporulating sulfate-reducing bacteria
Postgate, J. R., & Campbell, L. L. (1966) · Bacteriological Reviews · doi:10.1128/br.30.4.732-738.1966 · Cited by 222
AcrAB Multidrug Efflux Pump Regulation in Salmonella enterica serovar Typhimurium by RamA in Response to Environmental Signals
Nikaido, E., Yamaguchi, A., & Nishino, K. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804544200 · Cited by 221
Inhibitors of Pathogen Intercellular Signals as Selective Anti-Infective Compounds
Lesic, B., Lepine, F. L., Déziel, É., Zhang, J., Zhang, Q., Padfield, K. E., Castonguay, M., Milot, S. M., Stachel, S. E., Tzika, A. A., et al. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030126 · Cited by 221
Differential gene expression shows natural brominated furanones interfere with the autoinducer‐2 bacterial signaling system of Escherichia coli
Ren, D., Bedzyk, L. A., Ye, R. W., Thomas, S. M., & Wood, T. K. (2004) · Biotechnology and Bioengineering · doi:10.1002/bit.20259 · Cited by 220
A third envelope stress signal transduction pathway in Escherichia coli
Raffa, R. G., & Raivio, T. L. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03112.x · Cited by 216
Updating the H‐antigen classification ofBacillus thuringiensis
Mm, L., Frachon, E., Dumanoir, V. C., Ripouteau, H., Hamon, S., Laurent, P., & Thiéry, I. (1999) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.1999.00710.x · Cited by 200
Enterohemorrhagic Escherichia coli Biofilms Are Inhibited by 7-Hydroxyindole and Stimulated by Isatin
Lee, J., Bansal, T., Jayaraman, A., Bentley, W., & Wood, T. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00360-07 · Cited by 199
Regulation of autoinducer production in Salmonella typhimurium
Surette, M. G., & Bassler, B. L. (1999) · Molecular Microbiology · doi:10.1046/j.1365-2958.1999.01199.x · Cited by 198
Escherichia fergusonii and Enterobacter taylorae, two new species of Enterobacteriaceae isolated from clinical specimens
Farmer, J. J., Fanning, G. R., DAVIS, B. R., O'Hara, C. M., Riddle, C. F., Hickman-Brenner, F. W., ASBURY, M. A., Lowery, V. A., & Brenner, D. J. (1985) · Journal of Clinical Microbiology · doi:10.1128/jcm.21.1.77-81.1985 · Cited by 197
Cytotoxic enterotoxin produced by Aeromonas hydrophila: relationship of toxigenic isolates to diarrheal disease
Cumberbatch, N., Gurwith, M., Langston, C., Sack, R. B., & BRUNTON, J. L. (1979) · Infection and Immunity · doi:10.1128/iai.23.3.829-837.1979 · Cited by 182
Indole signalling contributes to the stable maintenance of Escherichia coli multicopy plasmids
Chant, E. L., & Summers, D. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05481.x · Cited by 182
Structure of the Escherichia coli Quorum Sensing Protein SdiA: Activation of the Folding Switch by Acyl Homoserine Lactones
Yao, Y., Martinez‐Yamout, M. A., Dickerson, T. J., Brogan, A. P., Wright, P. E., & Dyson, H. J. (2005) · Journal of Molecular Biology · doi:10.1016/j.jmb.2005.10.041 · Cited by 180
Indole Acts as an Extracellular Cue Regulating Gene Expression inVibrio cholerae
Mueller, R., Beyhan, S., Saini, S. G., Yildiz, F. H., & Bartlett, D. H. (2009) · Journal of Bacteriology · doi:10.1128/jb.01240-08 · Cited by 175
Orphan LuxR regulators of quorum sensing
Patankar, A. V., & González, J. E. (2009) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2009.00163.x · Cited by 173
Fusobacterium necrophorum: its characteristics and role as an animal pathogen
Langworth, B. (1977) · Bacteriological Reviews · doi:10.1128/br.41.2.373-390.1977 · Cited by 171
A Novel Protein-Deamidating Enzyme from Chryseobacterium proteolyticum sp. nov., a Newly Isolated Bacterium from Soil
Yamaguchi, S., & Yokoe, M. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.8.3337-3343.2000 · Cited by 171
Physiological studies of tryptophan transport and tryptophanase operon induction in Escherichia coli
Yanofsky, C., Horn, V., & Gollnick, P. D. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.19.6009-6017.1991 · Cited by 170
Severe infections caused by Propionibacterium acnes: an underestimated pathogen in late postoperative infections.
Jakab, E., Zbinden, R., Gubler, J., Ruef, C., von Graevenitz, A., & Krause, M. (1996) · PubMed Central · Cited by 163
Yersiniae other than , , and : the ignored species
Sulakvelidze, A. (2000) · Microbes and Infection · doi:10.1016/s1286-4579(00)00311-7 · Cited by 163
Nucleotide sequence of the structural gene for tryptophanase of Escherichia coli K-12
Deeley, M. C., & Yanofsky, C. (1981) · Journal of Bacteriology · doi:10.1128/jb.147.3.787-796.1981 · Cited by 161
Conservation of genes and processes controlled by the quorum response in bacteria: characterization of genes controlled by the quorum‐sensing transcription factor ComA in Bacillus subtilis
Comella, N., & Grossman, A. D. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04749.x · Cited by 158
Paralysis and killing of Caenorhabditis elegans by enteropathogenic Escherichia coli requires the bacterial tryptophanase gene
Anyanful, A., Dolan‐Livengood, J. M., Lewis, T., Sheth, S., DeZalia, M. N., Sherman, M. A., Kalman, L. V., Benian, G. M., & Kalman, D. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04739.x · Cited by 154
Temporal and Spatial Order of Events During the Induction of Cortical Cell Divisions in White Clover byRhizobium leguminosarumbv.trifoliiInoculation or Localized Cytokinin Addition
Mathesius, U., Charon, C., Rolfe, B. G., Kondorosi, Á., & Crespi, M. D. (2000) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi.2000.13.6.617 · Cited by 151
Tryptophanase: Structure, Catalytic Activities, and Mechanism of Action
Snell, E. E. (1975) · Advances in enzymology and related areas of molecular biology/Advances in enzymology and related subjects · doi:10.1002/9780470122877.ch6 · Cited by 148
Genome-Wide Analyses of Escherichia coli Gene Expression Responsive to the BaeSR Two-Component Regulatory System
Nishino, K., Honda, T., & Yamaguchi, A. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.5.1763-1772.2005 · Cited by 143
STUDIES ON THE ENTEROPATHOGENIC, FACULTATIVELY HALOPHILIC BACTERIA, VIBRIO PARAHAEMOLYTICUSI. MORPHOLOGICAL, CULTURAL AND BIOCHEMICAL PROPERTIES AND ITS TAXONOMICAL POSITION
Sakazaki, R., Iwanami, S., & FUKUMI, H. (1963) · Japanese Journal of Medical Science and Biology · doi:10.7883/yoken1952.16.161 · Cited by 137
Transfer of Kingella indologenes (Snell and Lapage 1976) to the Genus Suttonella gen. nov. as Suttonella indologenes comb. nov.; Transfer of Bacteroides nodosus (Beveridge 1941) to the Genus Dichelobacter gen. nov. as Dichelobacter nodosus comb. nov.; and Assignment of the Genera Cardiobacterium, Dichelobacter, and Suttonella to Cardiobacteriaceae fam. nov. in the Gamma Division of Proteobacteria on the Basis of 16S rRNA Sequence Comparisons
Dewhirst, F. E., Paster, B. J., Fontaine, S. L., & Rood, J. I. (1990) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-40-4-426 · Cited by 130
Vibrio pectenicida sp. nov., a pathogen of scallop (Pecten maximus) larvae
Christophe Lambert, B., Nicolas, J.-L., Cilia, V., & Corre, S. (1998) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-48-2-481 · Cited by 130
Indole cell signaling occurs primarily at low temperatures in Escherichia coli
Lee, J., Zhang, X., Hegde, M., Bentley, W. E., Jayaraman, A., & Wood, T. K. (2008) · The ISME Journal · doi:10.1038/ismej.2008.54 · Cited by 130
Reconfiguring the Quorum-Sensing Regulator SdiA ofEscherichia coliTo Control Biofilm Formation via Indole andN-Acylhomoserine Lactones
Lee, J., Maeda, T., Hong, S. H., & Wood, T. K. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02081-08 · Cited by 129
The promise and peril of transcriptional profiling in biofilm communities
An, D., & Parsek, M. R. (2007) · Current Opinion in Microbiology · doi:10.1016/j.mib.2007.05.011 · Cited by 127
Protein engineering of toluene ortho-monooxygenase of Burkholderia cepacia G4 for regiospecific hydroxylation of indole to form various indigoid compounds
Rui, L., Reardon, K. F., & Wood, T. K. (2004) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-004-1698-z · Cited by 125
Aeromonas salmonicida subsp. pectinolytica subsp. nov., a new pectinase-positive subspecies isolated from a heavily polluted river.
Paván, M. E., Abbott, S. L., Zorzópulos, J., & Janda, J. M. (2000) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-50-3-1119 · Cited by 123
Classification of Desulfovibrio species, the nonsporulating sulfate-reducing bacteria.
POSTGATE, J. R., & Campbell, L. L. (1966) · Bacteriological Reviews · doi:10.1128/mmbr.30.4.732-738.1966 · Cited by 119
STUDIES ON THE ENTEROPATHOGENIC, FACULTATIVELY HALOPHILIC BACTERIA, VIBRIO PARAHAEMOLYTICUS
Sakazaki, R., Iwanami, S., & Tamura, K. (1968) · Japanese Journal of Medical Science and Biology · doi:10.7883/yoken1952.21.313 · Cited by 118
Growth Phase-Dependent Expression of Drug Exporters in Escherichia coli and Its Contribution to Drug Tolerance
Kobayashi, A., Hirakawa, H., Hirata, T., Nishino, K., & Yamaguchi, A. (2006) · Journal of Bacteriology · doi:10.1128/jb.00217-06 · Cited by 118
Halogeometricum borinquense gen. nov., sp. nov., a novel halophilic archaeon from Puerto Rico
Montalvo‐Rodríguez, R., Vreeland, R. H., Oren, A., Kessel, M., Betancourt, C., & Lopez-Garriga, J. J. (1998) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-48-4-1305 · Cited by 117
Tryptophanase in Diverse Bacterial Species
Demoss, R. D., & Moser, K. W. (1969) · Journal of Bacteriology · doi:10.1128/jb.98.1.167-171.1969 · Cited by 114
Mapping Stress-Induced Changes in Autoinducer AI-2 Production in Chemostat-Cultivated Escherichia coli K-12
DeLisa, M. P., Valdés, J. J., & Bentley, W. E. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.9.2918-2928.2001 · Cited by 110
Identification of Clinical Isolates of Indole-Positive and Indole-Negative Klebsiella spp
Alves, M. S., Dias, R. C. D. S., Castro, A. C. D., Riley, L. W., & Moreira, B. M. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.00940-06 · Cited by 104
Secreted indole serves as a signal for expression of type III secretion system translocators in enterohaemorrhagic Escherichia coli O157 : H7
Hirakawa, H., Kodama, T., Takumi-Kobayashi, A., Honda, T., & Yamaguchi, A. (2009) · Microbiology · doi:10.1099/mic.0.020420-0 · Cited by 101
Role of multiple efflux pumps in Escherichia coli in indole expulsion
Kawamura‐Sato, K., Shibayama, K., Horii, T., Iimuma, Y., Arakawa, Y., & Ohta, M. (1999) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1999.tb08748.x · Cited by 101
Formation of Hydride-Meisenheimer Complexes of Picric Acid (2,4,6-Trinitrophenol) and 2,4-Dinitrophenol during Mineralization of Picric Acid by Nocardioides sp. Strain CB 22-2
Behrend, C., & Heesche‐Wagner, K. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.4.1372-1377.1999 · Cited by 100
Haloarcula spp able to biosynthesize exo- and endopolymers
Nicolaus, B., Lama, L., Esposito, E., Manca, M. C., Improta, R., Bellitti, M. R., Duckworth, A. W., Grant, W. D., & Gambacorta, A. (1999) · Journal of Industrial Microbiology & Biotechnology · doi:10.1038/sj.jim.2900738 · Cited by 99
The Biology of Hyphomicrobium and other Prosthecate, Budding Bacteria
Moore, R. L. (1981) · Annual Review of Microbiology · doi:10.1146/annurev.mi.35.100181.003031 · Cited by 99
Isolation and characterization of Edwardsiella tarda from fall chinook salmon (Oncorhynchus tshawytscha)
Amandi, A., Hiu, S. F., Rohovec, J. S., & Fryer, J. L. (1982) · Applied and Environmental Microbiology · doi:10.1128/aem.43.6.1380-1384.1982 · Cited by 98
Electrostatic Contributions to Indole−Lipid Interactions
Gaede, H. C., Yau, W., & Gawrisch, K. (2005) · The Journal of Physical Chemistry B · doi:10.1021/jp0511000 · Cited by 98
Structure and Function of the Escherichia coli Protein YmgB: A Protein Critical for Biofilm Formation and Acid-resistance
Lee, J., Page, R., García‐Contreras, R., Palermino, J.-M., Zhang, X., Doshi, O., Wood, T. K., & Peti, W. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.07.037 · Cited by 98
Symbiobacterium thermophilum gen. nov., sp. nov., a symbiotic thermophile that depends on co-culture with a Bacillus strain for growth.
Ohno, M., Shiratori‐Takano, H., Park, M. J., Saitoh, Y., Kumon, Y., Yamashita, N., Hirata, A., Nishida, H., Ueda, K., & Beppu, T. (2000) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-50-5-1829 · Cited by 98
New pathway for the biodegradation of indole in Aspergillus niger
Kamath, A. V., & Vaidyanathan, C. S. (1990) · Applied and Environmental Microbiology · doi:10.1128/aem.56.1.275-280.1990 · Cited by 97
Catabolite Repression of Tryptophanase in Escherichia coli
Botsford, J. L., & Demoss, R. D. (1971) · Journal of Bacteriology · doi:10.1128/jb.105.1.303-312.1971 · Cited by 97
Escherichia coli genes regulated by cell-to-cell signaling
Baca-DeLancey, R. R., South, M. M. T., Ding, X., & Rather, P. N. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.8.4610 · Cited by 97
Vibrio cholerae Strains Possess Multiple Strategies for Abiotic and Biotic Surface Colonization
Mueller, R., McDougald, D., Cusumano, D., Sodhi, N., Kjelleberg, S. J., Azam, F., & Bartlett, D. H. (2007) · Journal of Bacteriology · doi:10.1128/jb.01867-06 · Cited by 96
Low Concentrations of Diindolylmethane, a Metabolite of Indole-3-Carbinol, Protect against Oxidative Stress in a BRCA1-Dependent Manner
Fan, S., Meng, Q., Saha, T., Sarkar, F. H., & Rosen, E. M. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-3309 · Cited by 94
Isolation, Identification, and Molecular Characterization of Strains of Photorhabdus luminescens from Infected Humans in Australia
Peel, M. M., Alfredson, D. A., Gerrard, J. G., Davis, J. M., Robson, J. M. B., McDougall, R. J., Scullie, B. L., & Akhurst, R. J. (1999) · Journal of Clinical Microbiology · doi:10.1128/jcm.37.11.3647-3653.1999 · Cited by 91
Temporal regulation of enterohemorrhagic Escherichia coli virulence mediated by autoinducer-2
Bansal, T., Jesudhasan, P. R. R., Pillai, S. D., Wood, T. K., & Jayaraman, A. (2008) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-008-1359-8 · Cited by 86
PROPOSAL OF VIBRIO ALGINOLYTICUS FOR THE BIOTYPE 2 OF VIBRIO PARAHAEMOLYTICUS
Sakazaki, R. (1968) · Japanese Journal of Medical Science and Biology · doi:10.7883/yoken1952.21.359 · Cited by 86
Shewanella sediminis sp. nov., a novel Na+-requiring and hexahydro-1,3,5-trinitro-1,3,5-triazine-degrading bacterium from marine sediment
Zhao, J., Manno, D., Beaulieu, C., Paquet, L., & Hawari, J. A.-A. (2005) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63604-0 · Cited by 85
Altering Toluene 4-Monooxygenase by Active-Site Engineering for the Synthesis of 3-Methoxycatechol, Methoxyhydroquinone, and Methylhydroquinone
Tao, Y., Fishman, A., Bentley, W. E., & Wood, T. K. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.14.4705-4713.2004 · Cited by 81
Saturation Mutagenesis of Toluene ortho -Monooxygenase of Burkholderia cepacia G4 for Enhanced 1-Naphthol Synthesis and Chloroform Degradation
Rui, L., Kwon, Y. M., Fishman, A., Reardon, K. F., & Wood, T. K. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.6.3246-3252.2004 · Cited by 80
Fusobacterium necrophorum: its characteristics and role as an animal pathogen.
Langworth, B. (1977) · Bacteriological Reviews · doi:10.1128/mmbr.41.2.373-390.1977 · Cited by 79
Indole-positive Vibrio vulnificus isolated from disease outbreaks on a Danish eel farm
Dalsgaard, I., Høi, L., Siebeling, R. J., & Dalsgaard, A. (1999) · Diseases of Aquatic Organisms · doi:10.3354/dao035187 · Cited by 78
Controlling the Regiospecific Oxidation of Aromatics via Active Site Engineering of Toluene para-Monooxygenase of Ralstonia pickettii PKO1
Fishman, A., Tao, Y., Rui, L., & Wood, T. K. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m410320200 · Cited by 78
Degradation of indole by enrichment culture and Pseudomonas aeruginosa Gs isolated from mangrove sediment
Yin, B., Gu, J., & Wan, N.-S. (2005) · International Biodeterioration & Biodegradation · doi:10.1016/j.ibiod.2005.10.001 · Cited by 76
Indole-inducible proteins in bacteria suggest membrane and oxidant toxicity
Garbe, T. R., Kobayashi, M., & Yukawa, H. (2000) · Archives of Microbiology · doi:10.1007/s002030050012 · Cited by 74
The Tryptophanase Gene Cluster of Haemophilus influenzae Type b: Evidence for Horizontal Gene Transfer
Martin, K., Morlin, G., Smith, A. L., Nordyke, A., Eisenstark, A., & Golomb, M. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.1.107-118.1998 · Cited by 70
A MODIFICATION OF THE METHOD FOR DETERMINING THE PRODUCTION OF INDOL BY BACTERIA
Smith, T. (1897) · The Journal of Experimental Medicine · doi:10.1084/jem.2.5.543 · Cited by 70
Yersinia massiliensis sp. nov., isolated from fresh water
Merhej, V., Adékambi, T., Pagnier, I., Raoult, D., & Drancourt, M. (2008) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.65219-0 · Cited by 68
Oribacterium sinus gen. nov., sp. nov., within the family ‘Lachnospiraceae’ (phylum Firmicutes)
Carlier, J.-P., K'ouas, G., Bonne, I., Lozniewski, A., & Mory, F. (2004) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63060-0 · Cited by 67
Brachyspira hyodysenteriae and other strongly -haemolytic and indole-positive spirochaetes isolated from mallards (Anas platyrhynchos)
Jansson, D. S. (2004) · Journal of Medical Microbiology · doi:10.1099/jmm.0.05488-0 · Cited by 65
Transcription initiation at the tryptophanase promoter of Escherichia coli K-12
Deeley, M. C., & Yanofsky, C. (1982) · Journal of Bacteriology · doi:10.1128/jb.151.2.942-951.1982 · Cited by 63
Rapid presumptive identification of black-pigmented gram-negative anaerobic bacteria by using 4-methylumbelliferone derivatives
Moncla, B. J., Braham, P. H., Rabe, L. K., & Hillier, S. L. (1991) · Journal of Clinical Microbiology · doi:10.1128/jcm.29.9.1955-1958.1991 · Cited by 62
Isolation of an Escherichia coli strain mutant unable to form biofilm on polystyrene and to adhere to human pneumocyte cells: involvement of tryptophanase
Martino, P. D., Mérieau, A., Phillips, R. S., Orange, N., & Hulen, C. (2002) · Canadian Journal of Microbiology · doi:10.1139/w02-001 · Cited by 59
Formation and Interrelationships of Tryptophanase and Tryptophan Synthetases in Escherichia coli
Newton, W. A., & Snell, E. E. (1965) · Journal of Bacteriology · doi:10.1128/jb.89.2.355-364.1965 · Cited by 58
A Novel Indole Compound That Inhibits Pseudomonas aeruginosa Growth by Targeting MreB Is a Substrate for MexAB-OprM
Robertson, G. T., Doyle, T. B., Du, Q., Duncan, L. R., Mdluli, K. E., & Lynch, A. S. (2007) · Journal of Bacteriology · doi:10.1128/jb.00805-07 · Cited by 54
Analysis of Tryptophanase Operon Expression in Vitro
Gong, F., & Yanofsky, C. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201213200 · Cited by 53
Morphological and Biochemical Differentiation of Three Types of Small Oral Spirochetes
Socransky, S. S., Listgarten, M. A., Hubersak, C., Cotmore, J., & Clark, A. R. (1969) · Journal of Bacteriology · doi:10.1128/jb.98.3.878-882.1969 · Cited by 49
Biodegradation of indole at high concentration by persolvent fermentation with Pseudomonas sp. ST-200
Doukyu, N., & Aono, R. (1997) · Extremophiles · doi:10.1007/s007920050021 · Cited by 47
Pseudovibrio ascidiaceicola sp. nov., isolated from ascidians (sea squirts)
Fukunaga, Y., Kurahashi, M., Tanaka, K., Yanagi, K., Yokota, A., & Harayama, S. (2006) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63879-0 · Cited by 47
A comparison of various Haemophilus somnus strains.
Ga, G.-D., Pb, L., & Barnum, D. A. (1977) · PubMed · Cited by 42
Relatedness and Classification of Streptococcus mutans and "Mutans-like" Streptococci
SCHLEIFER, K. H., Kilpper-Bälz, R., Kraus, J., & Gehring, F. (1984) · Journal of Dental Research · doi:10.1177/00220345840630080701 · Cited by 42
The pyruvate kinase of Stigmatella aurantiaca is an indole binding protein and essential for development
Stamm, I., Lottspeich, F., & Plaga, W. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04640.x · Cited by 41
Larkinella insperata gen. nov., sp. nov., a bacterium of the phylum 'Bacteroidetes' isolated from water of a steam generator
Vancanneyt, M. (2006) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.63948-0 · Cited by 40
The effect of a single, temperature-sensitive mutation on global gene expression in Escherichia coli
LI, Y., Cole, K. B., & Altman, S. (2003) · RNA · doi:10.1261/rna.2198203 · Cited by 39
Isatin binding proteins in rat brain: In situ imaging, quantitative characterization of specific [3H]isatin binding, and proteomic profiling
Crumeyrolle‐Arias, M., Бунеева, О. А., Zgoda, V. G., Kopylov, A. T., Cardona, A., Tournaire, M., Pozdnev, V. F., Glover, V. A. S., & Medvedev, A. E. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22104 · Cited by 38
Induction of myxospores in Stigmatella aurantiaca (myxobacteria): inducers and inhibitors of myxospore formation, and mutants with a changed sporulation behaviour
Gerth, K., Metzger, R., & Reichenbach, H. (1993) · Journal of General Microbiology · doi:10.1099/00221287-139-4-865 · Cited by 36
Production and Isolation of Thermoviridin, an Antibiotic Produced by Thermoactinomyces viridis n. sp
Schuurmans, D. M., Olson, B. H., & Clemente, C. L. S. (1956) · Applied Microbiology · doi:10.1128/am.4.2.61-66.1956 · Cited by 32
Molecular Basis of the Indole-Negative Reaction in Shigella Strains: Extensive Damages to the tna Operon by Insertion Sequences
Rezwan, F., Lan, R., & Reeves, P. R. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.21.7460-7465.2004 · Cited by 32
Characteristics of Bacteroides isolates from the cecum of conventional mice
Tannock, G. W. (1977) · Applied and Environmental Microbiology · doi:10.1128/aem.33.4.745-750.1977 · Cited by 30
Production and Oxidation of Indole by Haemophilus influenzae
Stull, T. L., Hyun, L., Sharetzsky, C., Wooten, J., McCauley, J. P., & Smith, A. B. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.1.5 · Cited by 30
ISOLATION OF TOXIGENIC STRAINS OF CLOSTRIDIUM NOVYI FROM SOIL
Nishida, S., & Nakagawara, G. (1964) · Journal of Bacteriology · doi:10.1128/jb.88.6.1636-1640.1964 · Cited by 29
Introduction of ade novo bioremediation activity into anaerobic granular sludge using the dechlorinating bacterium DCB-2
Christiansen, N. M., & Ahring, B. K. (1996) · Antonie van Leeuwenhoek · doi:10.1007/bf00641612 · Cited by 29
Escherichia coli variants for gas and indole production at elevated incubation temperatures
Bueschkens, D. H., & Stiles, M. E. (1984) · Applied and Environmental Microbiology · doi:10.1128/aem.48.3.601-605.1984 · Cited by 28
Effect of growth conditions on production of violacein by Chromobacterium violaceum (BB-78 strain).
Maidana, R. L. B. R., Haun, M., & Durán, N. (1989) · PubMed · Cited by 28
Methods for identification of flavobacteria
Pickett, M. J. (1989) · Journal of Clinical Microbiology · doi:10.1128/jcm.27.10.2309-2315.1989 · Cited by 27
Morphological and Biochemical Characteristics of Aeromonas punctata ( hydrophila, liquefaciens ) Isolated from Human Sources
Gilardi, G. L. (1967) · Applied Microbiology · doi:10.1128/am.15.2.417-421.1967 · Cited by 26
Physiological Effects of a Constitutive Tryptophanase in Bacillus alvei
Hoch, J. A., & Demoss, R. D. (1965) · Journal of Bacteriology · doi:10.1128/jb.90.3.604-610.1965 · Cited by 25
Effect of miso soup containing Natto on the composition and metabolic activity of the human faecal flora
Fujisawa, T., Shinohara, K., Kishimoto, Y., & Terada, A. (2006) · Microbial Ecology in Health and Disease · doi:10.1080/08910600600931942 · Cited by 25
A New Group Of Enterobacteria, Possibly A New Citrobacter Sp.
Booth, E. V., & Mcdonald, S. (1971) · Journal of Medical Microbiology · doi:10.1099/00222615-4-3-329 · Cited by 24
Production of 3-Nitrosoindole Derivatives by Escherichia coli during Anaerobic Growth
Kwon, Y.-M., & Weiss, B. (2009) · Journal of Bacteriology · doi:10.1128/jb.00586-09 · Cited by 23
Identification of clinical isolates of indole-positive Klebsiella spp., including Klebsiella planticola, and a genetic and molecular analysis of their beta-lactamases
Liu, Y., Mee, B. J., & Mulgrave, L. (1997) · Journal of Clinical Microbiology · doi:10.1128/jcm.35.9.2365-2369.1997 · Cited by 22
Metabolites as Intercellular Signals for Regulation of Community-Level Traits
Monds, R. D., & O’Toole, G. A. (2014) · ASM Press eBooks · doi:10.1128/9781555815578.ch8 · Cited by 20
Production and Isolation of Thermoviridin, an Antibiotic Produced by Thermoactinomyces viridis n. sp1
Schuurmans, D. M., Olson, B. H., & Clemente, C. L. S. (1956) · Applied Microbiology · doi:10.1128/aem.4.2.61-66.1956 · Cited by 19
Sensitivity of Citrobacter freundii and Citrobacter koseri to cephalosporins and penicillins
Holmes, B., King, A., Phillips, I., & Lapage, S. P. (1974) · Journal of Clinical Pathology · doi:10.1136/jcp.27.9.729 · Cited by 17
The Effects of Acids, Alkalies, and Sugars on the Growth and Indole Formation of Bacillus coli
Wyeth, F. J. S. (1919) · Biochemical Journal · doi:10.1042/bj0130010 · Cited by 16
R/B Enteric Differential System for Identification of Enterobacteriaceae
Smith, P. B., Rhoden, D. L., Tomfohrde, K. M., Dunn, C., Balows, A., & Hermann, G. J. (1971) · Applied Microbiology · doi:10.1128/am.21.6.1036-1039.1971 · Cited by 15
The biochemical and cultural characteristics of Pasteurella pneumotropica.
Dj, S., & Simpson, W. (1977) · PubMed · Cited by 14
Morphological and Biochemical Characteristics of Aeromonas punctata (hydrophila, liquefaciens) Isolated from Human Sources
Gilardi, G. L. (1967) · Applied Microbiology · doi:10.1128/aem.15.2.417-421.1967 · Cited by 14
On the taxonomy, ecology and immunochemistry of genus Citrobacter.
Sedlák, J., Puchmayerová-Slajsová, M., Keleti, J., & Luderitz, O. (1971) · PubMed · Cited by 13
An equilibrium and calorimetric investigation of the hydrolysis of L-tryptophan to (indole + pyruvate + ammonia)
Tewari, Y. B., & Goldberg, R. N. (1994) · Journal of Solution Chemistry · doi:10.1007/bf00973544 · Cited by 13
Effect of miso soup containing Natto on the composition and metabolic activity of the human faecal flora
Fujisawa, T., Shinohara, K., Kishimoto, Y., & Terada, A. (2006) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v18i2.7691 · Cited by 12
Increased indole detection for Pasteurella multocida
Clemons, K. V., & Gadberry, J. L. (1982) · Journal of Clinical Microbiology · doi:10.1128/jcm.15.4.731-732.1982 · Cited by 10
5‐hydroxyoxindole, an indole metabolite, is present at high concentrations in brain
Crumeyrolle‐Arias, M., Tournaire, M., Rabot, S., Malpaux, B., & Thiéry, J. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21475 · Cited by 9
Tryptophan biosynthesis in the marine luminous bacterium Vibrio harveyi
Bieger, C. D., & Crawford, I. P. (1983) · Journal of Bacteriology · doi:10.1128/jb.153.2.884-894.1983 · Cited by 8
Practical Substitution for the Indole, Methyl Red, Voges-Proskauer, Citrate System
von Graevenitz, A. (1971) · Applied Microbiology · doi:10.1128/am.21.6.1107-1109.1971 · Cited by 6
[Isolation of Yersinia enterocolitica from drinking water in South Bavaria].
Pr, S. (1984) · PubMed · Cited by 5
Practical Substitution for the Indole, Methyl Red, Voges-Proskauer, Citrate System
von Graevenitz, A. (1971) · Applied Microbiology · doi:10.1128/aem.21.6.1107-1109.1971 · Cited by 4
Suppressive effects of lactulose and magnesium oxide supplementation on fecal putrefactive metabolites with shortening gastrointestinal transit time
Ishikado, A., Sato, T., & MITSUOKA, T. (2007) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v19i3.7653 · Cited by 3

Research works printed but not linked: 1

Pittard AJ (1996) Biosynthesis of the aromatic amino acids: the tryptophan pathway. Escherichia coli and Salmonella: Cellular and Molecular Biology ( Neidhardt FC , ed), pp. 458–484. ASM Press, Washington, DC.

Sorted by citations

Microbial tryptophan catabolites in health and disease
Roager, H. M., & Licht, T. R. (2018) · Nature Communications · doi:10.1038/s41467-018-05470-4 · Cited by 2,236
Serotonin, tryptophan metabolism and the brain-gut-microbiome axis
O’Mahony, S. M., Clarke, G., Borre, Y. E., Dinan, T. G., & Cryan, J. F. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.027 · Cited by 2,012
Tryptophan metabolism as a common therapeutic target in cancer, neurodegeneration and beyond
Platten, M., Nollen, E. A. A., Röhrig, U. F., Fallarino, F., & Opitz, C. A. (2019) · Nature Reviews Drug Discovery · doi:10.1038/s41573-019-0016-5 · Cited by 1,586
Minireview: Gut microbiota: The neglected endocrine organ
Clarke, G., Stilling, R. M., Kennedy, P. J., Stanton, C., Cryan, J. F., & Dinan, T. G. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1108 · Cited by 1,192
Auxin and Plant-Microbe InteractionsPreprint
Spaepen, S., & Vanderleyden, J. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001438 · Cited by 1,225

See all 1,059

Authors: Lee, J.-H., & Lee, J.
Affiliations: Yeungnam University (KR)
Corresponding author: Lee, Jintae
ORCID: Lee, Jin-Hyung
Lee, Jintae
Venue: FEMS Microbiology Reviews
Publisher: Oxford University Press (OUP)
Published: 2010-07
Volume: 34
Issue: 4
Pages: 426-444
ISSN: 0168-6445 (ISSN-L)
1574-6976
DOI: 10.1111/j.1574-6976.2009.00204.x
OpenAlex: W2049821596
Cited by: 1,059
References: 174
Citations by year: 2026: 82 · 2025: 113 · 2024: 94 · 2023: 115 · 2022: 112 · 2021: 99 · 2020: 89 · 2019: 62 · 2018: 61 · 2017: 42 · 2016: 36 · 2015: 44 · 2014: 42 · 2013: 27 · 2012: 17
FWCI: 1.02
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: FEMS Microbiology Reviews (publishedVersion)
PubMed (publishedVersion)
Funders: Yeungnam University
Directorate for Education and Human Resources
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Life Sciences › Immunology and Microbiology › Microbiology › Escherichia coli research studies
Keywords: intercellular communication, bacterial quorum sensing, microbial communities, sporulation, plasmid stability, drug resistance, biofilm formation, virulence, Gram-positive bacteria, Gram-negative bacteria
MeSH terms: Bacteria, Indoles, Plasmids, Virulence, Signal Transduction, Gene Expression Regulation, Bacterial, Bacterial Physiological Phenomena, Biofilms, Drug Resistance, Bacterial, Quorum Sensing

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Indole as an intercellular signal in microbial communities

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks