KEGG   PATHWAY: sdv02024
Entry
sdv02024                    Pathway                                
Name
Quorum sensing - Streptomyces davaonensis
Description
Quorum sensing (QS) is a regulatory system that allows bacteria to share information about cell density and adjust gene expression accordingly. All QS bacteria produce and release chemical signal molecules called autoinducers (AIs) that increase in concentration as a function of cell density. The most commonly studied AIs belong to one of the following three categories: acylated homoserine lactones, also referred to as AI-1, used by Gram-negative bacteria; peptide signals, used by Gram-positive bacteria; and AI-2, used by both Gram-negative and Gram-positive bacteria. QS can be divided into at least 4 steps: production of AIs by the bacterial cell; release of AIs, either actively or passively, into the surrounding environment; recognition of AIs by specific receptors; and leading to changes in gene regulation once they exceed a threshold concentration. The processes controlled by QS include virulence, competence, conjugation, antibiotic production, motility, sporulation, and biofilm formation.
Class
Cellular Processes; Cellular community - prokaryotes
Pathway map
sdv02024  Quorum sensing
sdv02024

Other DBs
GO: 0009372
Organism
Streptomyces davaonensis [GN:sdv]
Gene
BN159_6401  trpE; Anthranilate synthase component 1 [KO:K01657] [EC:4.1.3.27]
BN159_4437  aroH1; Phospho-2-dehydro-3-deoxyheptonate aldolase [KO:K01626] [EC:2.5.1.54]
BN159_6322  aroH3; Phospho-2-dehydro-3-deoxyheptonate aldolase [KO:K01626] [EC:2.5.1.54]
BN159_6319  phzB; Anthranilate synthase, phenazine specific [KO:K13063] [EC:2.6.1.86]
BN159_2583  kdpE1; KDP operon transcriptional regulatory protein kdpE [KO:K07667]
BN159_7226  kdpE3; KDP operon transcriptional regulatory protein kdpE [KO:K07667]
BN159_4069  Glutamate decarboxylase [KO:K01580] [EC:4.1.1.15]
BN159_7127  substrate-binding transporter [KO:K02055]
BN159_7129  binding-protein-dependent transport system inner membrane component [KO:K02053]
BN159_7128  ABC transporter [KO:K02054]
BN159_7130  potA3; Spermidine/putrescine import ATP-binding protein PotA [KO:K02052]
BN159_6459  periplasmic branched-chain amino acid-binding protein [KO:K01999]
BN159_4966  lipoprotein [KO:K01999]
BN159_0904  branched-chain amino acid ABC transporter [KO:K01997]
BN159_6458  livH; High-affinity branched-chain amino acid transport system permease protein livH [KO:K01997]
BN159_0903  branched-chain amino acid ABC transport permease [KO:K01998]
BN159_6457  branched-chain amino acid ABC transporter permease [KO:K01998]
BN159_0905  high-affinity branched-chain amino acid transport ATP-binding protein [KO:K01995]
BN159_6456  livG; High-affinity branched-chain amino acid transport ATP-binding protein LivG [KO:K01995]
BN159_0906  livF1; High-affinity branched-chain amino acid transport ATP-binding protein LivF [KO:K01996]
BN159_6795  urea ABC transporter, ATP-binding protein UrtE [KO:K01996]
BN159_6455  livF3; High-affinity branched-chain amino acid transport ATP-binding protein LivF [KO:K01996]
BN159_1370  hypothetical protein [KO:K13075] [EC:3.1.1.81]
BN159_6622  pel; Pectate lyase [KO:K01728] [EC:4.2.2.2]
BN159_7504  Pectate lyase/Amb allergen [KO:K01728] [EC:4.2.2.2]
BN159_5850  neutral zinc metalloprotease [KO:K20273]
BN159_4868  preprometalloendoprotease [KO:K20273]
BN159_2956  neutral zinc metalloprotease [KO:K20273]
BN159_7447  hypothetical protein [KO:K20276]
BN159_8165  O-succinylbenzoate-CoA ligase [KO:K01897] [EC:6.2.1.3]
BN159_1879  fadD15; Long-chain-fatty-acid--CoA ligase FadD15 [KO:K01897] [EC:6.2.1.3]
BN159_1255  lcfB; Long-chain-fatty-acid--CoA ligase [KO:K01897] [EC:6.2.1.3]
BN159_5572  fadD15; Long-chain-fatty-acid--CoA ligase FadD15 [KO:K01897] [EC:6.2.1.3]
BN159_6879  dicarboxylate-CoA ligase PimA [KO:K01897] [EC:6.2.1.3]
BN159_3887  fadD15; Long-chain-fatty-acid--CoA ligase FadD15 [KO:K01897] [EC:6.2.1.3]
BN159_8317  long-chain-fatty-acid-CoA ligase [KO:K01897] [EC:6.2.1.3]
BN159_6303  fadD15; Long-chain-fatty-acid--CoA ligase FadD15 [KO:K01897] [EC:6.2.1.3]
BN159_5734  long-chain-fatty-acid-CoA ligase [KO:K01897] [EC:6.2.1.3]
BN159_4141  transcriptional regulator [KO:K10914]
BN159_6591  hypothetical protein [KO:K10914]
BN159_5046  secreted beta-mannosidase [KO:K01218] [EC:3.2.1.78]
BN159_1463  ToxA protein [KO:K20331] [EC:2.1.1.349]
BN159_4727  ribA3; GTP cyclohydrolase II [KO:K01497] [EC:3.5.4.25]
BN159_1827  ribA1; GTP cyclohydrolase-2 [KO:K01497] [EC:3.5.4.25]
BN159_3287  peptide ABC transporter substrate-binding protein [KO:K15580]
BN159_3286  oppB2; oligopeptide ABC transporter substrate-binding protein [KO:K15581]
BN159_3285  peptide ABC transporter, permease [KO:K15582]
BN159_3284  oppD3; Oligopeptide transport ATP-binding protein OppD [KO:K15583]
BN159_3283  appF3; Oligopeptide transport ATP-binding protein AppF [KO:K10823]
BN159_2317  solute-binding protein [KO:K02035]
BN159_3558  oligopeptide binding protein [KO:K02035]
BN159_1837  solute-binding lipoprotein [KO:K02035]
BN159_3235  ABC transporter solute-binding protein [KO:K02035]
BN159_3289  bldKB1; ABC transporter protein BldKB [KO:K02035]
BN159_3297  bldKB2; ABC transporter protein [KO:K02035]
BN159_3300  lipoprotein [KO:K02035]
BN159_2929  ABC transporter solute-binding protein [KO:K02035]
BN159_5785  ABC transporter substrate-binding protein [KO:K02035]
BN159_7258  solute binding transport lipoprotein [KO:K02035]
BN159_6927  lipoprotein oligopeptide binding protein [KO:K02035]
BN159_6928  solute binding transport lipoprotein [KO:K02035]
BN159_7773  ABC transporter, solute-binding protein [KO:K02035]
BN159_2316  glutathione transport system permease gsiC [KO:K02033]
BN159_1836  transport system permease [KO:K02033 K02034]
BN159_3233  nickel ABC transporter, permease subunit NikB [KO:K02033]
BN159_3290  bldKC1; ABC transporter integral membrane protein BldKC [KO:K02033]
BN159_3296  bldKC2; ABC transporter integral membrane protein [KO:K02033]
BN159_2928  dppB; ABC transporter permease protein [KO:K02033]
BN159_5784  nickel ABC transporter, permease subunit NikB [KO:K02033]
BN159_7772  dipeptide/oligopeptide ABC transporter inner membrane subunit [KO:K02033]
BN159_2315  ABC transporter transmembrane protein [KO:K02034]
BN159_3234  nickel ABC transporter, permease subunit NikC [KO:K02034]
BN159_3288  bldKA1; ABC transporter integral membrane protein BldKA [KO:K02034]
BN159_3298  bldKA2; ABC transporter integral membrane protein [KO:K02034]
BN159_2930  appC; ABC transporter permease protein [KO:K02034]
BN159_7771  binding-protein-dependent transporters inner membrane component [KO:K02034]
BN159_5783  ABC transporter permease [KO:K02031 K02034]
BN159_2927  oppD1; Oligopeptide transport ATP-binding protein OppD [KO:K02031]
BN159_3232  gsiA; Glutathione import ATP-binding protein GsiA [KO:K02031 K02032]
BN159_2314  oligopeptide/dipeptide ABC transporter,ATP-binding protein [KO:K02031 K02032]
BN159_3291  oppD5; Oligopeptide transport ATP-binding protein OppD [KO:K02031]
BN159_7770  yejF; putative ABC transporter ATP-binding protein YejF [KO:K02031 K02032]
BN159_3295  dppD; Dipeptide transport ATP-binding protein DppD [KO:K02031]
BN159_2926  appF1; Oligopeptide transport ATP-binding protein AppF [KO:K02032]
BN159_3294  appF7; Oligopeptide transport ATP-binding protein AppF [KO:K02032]
BN159_5782  D-methionine ABC transporter, ATP-binding protein [KO:K02032]
BN159_5415  hypothetical protein [KO:K03217]
BN159_4528  oxaA; Membrane protein oxaA [KO:K03217]
BN159_2282  bprV; Extracellular basic protease [KO:K14645] [EC:3.4.21.-]
BN159_3746  putative membrane protein [KO:K03073]
BN159_6538  putative secreted protein [KO:K03075]
BN159_3704  secY; Preprotein translocase subunit secY [KO:K03076]
BN159_7072  secreted protein [KO:K03210]
BN159_5288  secA; Protein translocase subunit secA [KO:K03070] [EC:7.4.2.8]
BN159_2812  ftsY; Cell division protein [KO:K03110]
BN159_2806  ffh; Signal recognition particle protein [KO:K03106] [EC:3.6.5.4]
BN159_1732  plcN; Non-hemolytic phospholipase C [KO:K01114] [EC:3.1.4.3]
BN159_7742  lantibiotic dehydratase-like protein [KO:K20483] [EC:3.13.2.4]
BN159_7741  lanthionine synthetase C-like protein [KO:K20484] [EC:3.13.2.4]
Compound
C00007  Oxygen
C00009  Orthophosphate
C00059  Sulfate
C00232  Succinate semialdehyde
C00334  4-Aminobutanoate
C00547  L-Noradrenaline
C00788  L-Adrenaline
C01019  L-Fucose
C11837  N-Butyryl-L-homoserine lactone
C11841  N-(3-Oxooctanoyl)homoserine lactone
C11844  N-Heptanoylhomoserine lactone
C11845  N-(3-Hydroxy-7-cis-tetradecenoyl)homoserine lactone
C11848  2-Heptyl-3-hydroxy-quinolone
C16421  AI-2
C16463  3',5'-Cyclic diGMP
C16640  CAI-1
C18049  N-Acyl-L-homoserine lactone
C18206  cis-11-Methyl-2-dodecenoic acid
C20643  2-Heptyl-4(1H)-quinolone
C20677  N-(4-Coumaroyl)-L-homoserine lactone
C20959  (4S)-4-Hydroxy-5-phosphooxypentane-2,3-dione
C21195  N-(3-Hydroxybutanoyl)-L-homoserine lactone
C21197  N-Hexanoyl-L-homoserine lactone
C21198  N-(3-Oxohexanoyl)-L-homoserine lactone
C21199  N-Octanoyl-L-homoserine lactone
C21200  N-3-Hydroxyoctanoyl-L-homoserine lactone
C21201  N-3-Oxo-dodecanoyl-L-homoserine lactone
C21202  cis-2-Dodecenoic acid
C21220  AIP-1
C21221  CSP
C21222  CSP
C21223  Blp
C21224  SHP2
C21225  SHP3
C21226  cCF10
C21227  iCF10
C21228  cAD1
C21229  iAD1
C21230  ComX pheromone
C21231  PhrA pentapeptide
C21232  PhrC pentapeptide
C21233  PhrE pentapeptide
C21234  PhrF pentapeptide
C21235  PhrG pentapeptide
C21236  PhrH pentapeptide
C21237  PhrK pentapeptide
C21238  NprX peptide
C21239  PapR peptide
C21241  AIP-2
C21242  AIP-3
C21243  AIP-4
C21244  AgrD peptide
C21245  AgrD1 peptide
C21246  GBAP
C21382  R-THMF
Reference
  Authors
Pereira CS, Thompson JA, Xavier KB
  Title
AI-2-mediated signalling in bacteria.
  Journal
FEMS Microbiol Rev 37:156-81 (2013)
DOI:10.1111/j.1574-6976.2012.00345.x
Reference
  Authors
Verma SC, Miyashiro T
  Title
Quorum sensing in the squid-Vibrio symbiosis.
  Journal
Int J Mol Sci 14:16386-401 (2013)
DOI:10.3390/ijms140816386
Reference
  Authors
Norsworthy AN, Visick KL
  Title
Gimme shelter: how Vibrio fischeri successfully navigates an animal's multiple environments.
  Journal
Front Microbiol 4:356 (2013)
DOI:10.3389/fmicb.2013.00356
Reference
  Authors
Papaioannou E, Utari PD, Quax WJ
  Title
Choosing an appropriate infection model to study quorum sensing inhibition in Pseudomonas infections.
  Journal
Int J Mol Sci 14:19309-40 (2013)
DOI:10.3390/ijms140919309
Reference
  Authors
Heeb S, Fletcher MP, Chhabra SR, Diggle SP, Williams P, Camara M
  Title
Quinolones: from antibiotics to autoinducers.
  Journal
FEMS Microbiol Rev 35:247-74 (2011)
DOI:10.1111/j.1574-6976.2010.00247.x
Reference
  Authors
Rasamiravaka T, Labtani Q, Duez P, El Jaziri M
  Title
The formation of biofilms by Pseudomonas aeruginosa: a review of the natural and synthetic compounds interfering with control mechanisms.
  Journal
Biomed Res Int 2015:759348 (2015)
DOI:10.1155/2015/759348
Reference
  Authors
Whiteley M, Greenberg EP
  Title
Promoter specificity elements in Pseudomonas aeruginosa quorum-sensing-controlled genes.
  Journal
J Bacteriol 183:5529-34 (2001)
DOI:10.1128/JB.183.19.5529-5534.2001
Reference
  Authors
Chin-A-Woeng TF, van den Broek D, de Voer G, van der Drift KM, Tuinman S, Thomas-Oates JE, Lugtenberg BJ, Bloemberg GV
  Title
Phenazine-1-carboxamide production in the biocontrol strain Pseudomonas chlororaphis PCL1391 is regulated by multiple factors secreted into the growth medium.
  Journal
Mol Plant Microbe Interact 14:969-79 (2001)
DOI:10.1094/MPMI.2001.14.8.969
Reference
  Authors
Hughes DT, Clarke MB, Yamamoto K, Rasko DA, Sperandio V
  Title
The QseC adrenergic signaling cascade in Enterohemorrhagic E. coli (EHEC).
  Journal
PLoS Pathog 5:e1000553 (2009)
DOI:10.1371/journal.ppat.1000553
Reference
  Authors
Njoroge J, Sperandio V
  Title
Enterohemorrhagic Escherichia coli virulence regulation by two bacterial adrenergic kinases, QseC and QseE.
  Journal
Infect Immun 80:688-703 (2012)
DOI:10.1128/IAI.05921-11
Reference
  Authors
Pacheco AR, Curtis MM, Ritchie JM, Munera D, Waldor MK, Moreira CG, Sperandio V
  Title
Fucose sensing regulates bacterial intestinal colonization.
  Journal
Nature 492:113-7 (2012)
DOI:10.1038/nature11623
Reference
  Authors
Hirakawa H, Harwood CS, Pechter KB, Schaefer AL, Greenberg EP
  Title
Antisense RNA that affects Rhodopseudomonas palustris quorum-sensing signal receptor expression.
  Journal
Proc Natl Acad Sci U S A 109:12141-6 (2012)
DOI:10.1073/pnas.1200243109
Reference
  Authors
Danino VE, Wilkinson A, Edwards A, Downie JA
  Title
Recipient-induced transfer of the symbiotic plasmid pRL1JI in Rhizobium leguminosarum bv. viciae is regulated by a quorum-sensing relay.
  Journal
Mol Microbiol 50:511-25 (2003)
DOI:10.1046/j.1365-2958.2003.03699.x
Reference
  Authors
Wisniewski-Dye F, Downie JA
  Title
Quorum-sensing in Rhizobium.
  Journal
Antonie Van Leeuwenhoek 81:397-407 (2002)
DOI:10.1023/A:1020501104051
Reference
  Authors
Rodelas B, Lithgow JK, Wisniewski-Dye F, Hardman A, Wilkinson A, Economou A, Williams P, Downie JA
  Title
Analysis of quorum-sensing-dependent control of rhizosphere-expressed (rhi) genes in Rhizobium leguminosarum bv. viciae.
  Journal
J Bacteriol 181:3816-23 (1999)
DOI:10.1128/JB.181.12.3816-3823.1999
Reference
  Authors
Lang J, Faure D
  Title
Functions and regulation of quorum-sensing in Agrobacterium tumefaciens.
  Journal
Front Plant Sci 5:14 (2014)
DOI:10.3389/fpls.2014.00014
Reference
  Authors
Planamente S, Morera S, Faure D
  Title
In planta fitness-cost of the Atu4232-regulon encoding for a selective GABA-binding sensor in Agrobacterium.
  Journal
Commun Integr Biol 6:e23692 (2013)
DOI:10.4161/cib.23692
Reference
  Authors
Barnard AM, Salmond GP
  Title
Quorum sensing in Erwinia species.
  Journal
Anal Bioanal Chem 387:415-23 (2007)
DOI:10.1007/s00216-006-0701-1
Reference
  Authors
Barnard AM, Bowden SD, Burr T, Coulthurst SJ, Monson RE, Salmond GP
  Title
Quorum sensing, virulence and secondary metabolite production in plant soft-rotting bacteria.
  Journal
Philos Trans R Soc Lond B Biol Sci 362:1165-83 (2007)
DOI:10.1098/rstb.2007.2042
Reference
  Authors
Carlier A, Burbank L, von Bodman SB
  Title
Identification and characterization of three novel EsaI/EsaR quorum-sensing controlled stewartan exopolysaccharide biosynthetic genes in Pantoea stewartii ssp. stewartii.
  Journal
Mol Microbiol 74:903-13 (2009)
DOI:10.1111/j.1365-2958.2009.06906.x
Reference
PMID:7665477
  Authors
Beck von Bodman S, Farrand SK
  Title
Capsular polysaccharide biosynthesis and pathogenicity in Erwinia stewartii require induction by an N-acylhomoserine lactone autoinducer.
  Journal
J Bacteriol 177:5000-8 (1995)
DOI:10.1128/JB.177.17.5000-5008.1995
Reference
  Authors
O'Grady EP, Viteri DF, Malott RJ, Sokol PA
  Title
Reciprocal regulation by the CepIR and CciIR quorum sensing systems in Burkholderia cenocepacia.
  Journal
BMC Genomics 10:441 (2009)
DOI:10.1186/1471-2164-10-441
Reference
  Authors
Malott RJ, Baldwin A, Mahenthiralingam E, Sokol PA
  Title
Characterization of the cciIR quorum-sensing system in Burkholderia cenocepacia.
  Journal
Infect Immun 73:4982-92 (2005)
DOI:10.1128/IAI.73.8.4982-4992.2005
Reference
  Authors
Deng Y, Schmid N, Wang C, Wang J, Pessi G, Wu D, Lee J, Aguilar C, Ahrens CH, Chang C, Song H, Eberl L, Zhang LH
  Title
Cis-2-dodecenoic acid receptor RpfR links quorum-sensing signal perception with regulation of virulence through cyclic dimeric guanosine monophosphate turnover.
  Journal
Proc Natl Acad Sci U S A 109:15479-84 (2012)
DOI:10.1073/pnas.1205037109
Reference
  Authors
Suppiger A, Schmid N, Aguilar C, Pessi G, Eberl L
  Title
Two quorum sensing systems control biofilm formation and virulence in members of the Burkholderia cepacia complex.
  Journal
Virulence 4:400-9 (2013)
DOI:10.4161/viru.25338
Reference
  Authors
Deng Y, Wu J, Tao F, Zhang LH
  Title
Listening to a new language: DSF-based quorum sensing in Gram-negative bacteria.
  Journal
Chem Rev 111:160-73 (2011)
DOI:10.1021/cr100354f
Reference
  Authors
Ryan RP, Dow JM
  Title
Communication with a growing family: diffusible signal factor (DSF) signaling in bacteria.
  Journal
Trends Microbiol 19:145-52 (2011)
DOI:10.1016/j.tim.2010.12.003
Reference
  Authors
Kim J, Kim JG, Kang Y, Jang JY, Jog GJ, Lim JY, Kim S, Suga H, Nagamatsu T, Hwang I
  Title
Quorum sensing and the LysR-type transcriptional activator ToxR regulate toxoflavin biosynthesis and transport in Burkholderia glumae.
  Journal
Mol Microbiol 54:921-34 (2004)
DOI:10.1111/j.1365-2958.2004.04338.x
Reference
  Authors
Kim J, Kang Y, Choi O, Jeong Y, Jeong JE, Lim JY, Kim M, Moon JS, Suga H, Hwang I
  Title
Regulation of polar flagellum genes is mediated by quorum sensing and FlhDC in Burkholderia glumae.
  Journal
Mol Microbiol 64:165-79 (2007)
DOI:10.1111/j.1365-2958.2007.05646.x
Reference
  Authors
Stauff DL, Bassler BL
  Title
Quorum sensing in Chromobacterium violaceum: DNA recognition and gene regulation by the CviR receptor.
  Journal
J Bacteriol 193:3871-8 (2011)
DOI:10.1128/JB.05125-11
Reference
  Authors
Chen G, Swem LR, Swem DL, Stauff DL, O'Loughlin CT, Jeffrey PD, Bassler BL, Hughson FM
  Title
A strategy for antagonizing quorum sensing.
  Journal
Mol Cell 42:199-209 (2011)
DOI:10.1016/j.molcel.2011.04.003
Reference
  Authors
Hao G, Burr TJ
  Title
Regulation of long-chain N-acyl-homoserine lactones in Agrobacterium vitis.
  Journal
J Bacteriol 188:2173-83 (2006)
DOI:10.1128/JB.188.6.2173-2183.2006
Reference
  Authors
Savka MA, Le PT, Burr TJ
  Title
LasR receptor for detection of long-chain quorum-sensing signals: identification of N-acyl-homoserine lactones encoded by the avsI locus of Agrobacterium vitis.
  Journal
Curr Microbiol 62:101-10 (2011)
DOI:10.1007/s00284-010-9679-1
Reference
  Authors
Le KY, Otto M
  Title
Quorum-sensing regulation in staphylococci-an overview.
  Journal
Front Microbiol 6:1174 (2015)
DOI:10.3389/fmicb.2015.01174
Reference
  Authors
Queck SY, Jameson-Lee M, Villaruz AE, Bach TH, Khan BA, Sturdevant DE, Ricklefs SM, Li M, Otto M
  Title
RNAIII-independent target gene control by the agr quorum-sensing system: insight into the evolution of virulence regulation in Staphylococcus aureus.
  Journal
Mol Cell 32:150-8 (2008)
DOI:10.1016/j.molcel.2008.08.005
Reference
  Authors
Darkoh C, DuPont HL, Norris SJ, Kaplan HB
  Title
Toxin synthesis by Clostridium difficile is regulated through quorum signaling.
  Journal
MBio 6:e02569 (2015)
DOI:10.1128/mBio.02569-14
Reference
  Authors
Vidal JE, Shak JR, Canizalez-Roman A
  Title
The CpAL quorum sensing system regulates production of hemolysins CPA and PFO to build Clostridium perfringens biofilms.
  Journal
Infect Immun 83:2430-42 (2015)
DOI:10.1128/IAI.00240-15
Reference
  Authors
Ohtani K, Yuan Y, Hassan S, Wang R, Wang Y, Shimizu T
  Title
Virulence gene regulation by the agr system in Clostridium perfringens.
  Journal
J Bacteriol 191:3919-27 (2009)
DOI:10.1128/JB.01455-08
Reference
  Authors
Li YH, Tian X
  Title
Quorum sensing and bacterial social interactions in biofilms.
  Journal
Sensors (Basel) 12:2519-38 (2012)
DOI:10.3390/s120302519
Reference
  Authors
Berg KH, Biornstad TJ, Johnsborg O, Havarstein LS
  Title
Properties and biological role of streptococcal fratricins.
  Journal
Appl Environ Microbiol 78:3515-22 (2012)
DOI:10.1128/AEM.00098-12
Reference
  Authors
Conrads G, de Soet JJ, Song L, Henne K, Sztajer H, Wagner-Dobler I, Zeng AP
  Title
Comparing the cariogenic species Streptococcus sobrinus and S. mutans on whole genome level.
  Journal
J Oral Microbiol 6:26189 (2014)
DOI:10.3402/jom.v6.26189
Reference
  Authors
Jimenez JC, Federle MJ
  Title
Quorum sensing in group A Streptococcus.
  Journal
Front Cell Infect Microbiol 4:127 (2014)
DOI:10.3389/fcimb.2014.00127
Reference
  Authors
Cook LC, Federle MJ
  Title
Peptide pheromone signaling in Streptococcus and Enterococcus.
  Journal
FEMS Microbiol Rev 38:473-92 (2014)
DOI:10.1111/1574-6976.12046
Reference
PMID:9680220
  Authors
Podbielski A, Leonard BA
  Title
The group A streptococcal dipeptide permease (Dpp) is involved in the uptake of essential amino acids and affects the expression of cysteine protease.
  Journal
Mol Microbiol 28:1323-34 (1998)
DOI:10.1046/j.1365-2958.1998.00898.x
Reference
PMID:8885277
  Authors
Podbielski A, Pohl B, Woischnik M, Korner C, Schmidt KH, Rozdzinski E, Leonard BA
  Title
Molecular characterization of group A streptococcal (GAS) oligopeptide permease (opp) and its effect on cysteine protease production.
  Journal
Mol Microbiol 21:1087-99 (1996)
DOI:10.1046/j.1365-2958.1996.661421.x
Reference
  Authors
Anbalagan S, Dmitriev A, McShan WM, Dunman PM, Chaussee MS
  Title
Growth phase-dependent modulation of Rgg binding specificity in Streptococcus pyogenes.
  Journal
J Bacteriol 194:3961-71 (2012)
DOI:10.1128/JB.06709-11
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  Authors
Clewell DB
  Title
Tales of conjugation and sex pheromones: A plasmid and enterococcal odyssey.
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Mob Genet Elements 1:38-54 (2011)
DOI:10.4161/mge.1.1.15409
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Wardal E, Sadowy E, Hryniewicz W
  Title
Complex nature of enterococcal pheromone-responsive plasmids.
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Pol J Microbiol 59:79-87 (2010)
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Roux A, Payne SM, Gilmore MS
  Title
Microbial telesensing: probing the environment for friends, foes, and food.
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Cell Host Microbe 6:115-24 (2009)
DOI:10.1016/j.chom.2009.07.004
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  Authors
Slamti L, Perchat S, Huillet E, Lereclus D
  Title
Quorum sensing in Bacillus thuringiensis is required for completion of a full infectious cycle in the insect.
  Journal
Toxins (Basel) 6:2239-55 (2014)
DOI:10.3390/toxins6082239
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Lopez D, Kolter R
  Title
Extracellular signals that define distinct and coexisting cell fates in Bacillus subtilis.
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FEMS Microbiol Rev 34:134-49 (2010)
DOI:10.1111/j.1574-6976.2009.00199.x
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Stephenson S, Mueller C, Jiang M, Perego M
  Title
Molecular analysis of Phr peptide processing in Bacillus subtilis.
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J Bacteriol 185:4861-71 (2003)
DOI:10.1128/JB.185.16.4861-4871.2003
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  Authors
Lanigan-Gerdes S, Dooley AN, Faull KF, Lazazzera BA
  Title
Identification of subtilisin, Epr and Vpr as enzymes that produce CSF, an extracellular signalling peptide of Bacillus subtilis.
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Mol Microbiol 65:1321-33 (2007)
DOI:10.1111/j.1365-2958.2007.05869.x
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  Authors
Kleerebezem M
  Title
Quorum sensing control of lantibiotic production; nisin and subtilin autoregulate their own biosynthesis.
  Journal
Peptides 25:1405-14 (2004)
DOI:10.1016/j.peptides.2003.10.021
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  Authors
Rutherford ST, Bassler BL
  Title
Bacterial quorum sensing: its role in virulence and possibilities for its control.
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Cold Spring Harb Perspect Med 2:a012427 (2012)
DOI:10.1101/cshperspect.a012427
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  Authors
LaSarre B, Federle MJ
  Title
Exploiting quorum sensing to confuse bacterial pathogens.
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Microbiol Mol Biol Rev 77:73-111 (2013)
DOI:10.1128/MMBR.00046-12
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  Authors
Sifri CD
  Title
Healthcare epidemiology: quorum sensing: bacteria talk sense.
  Journal
Clin Infect Dis 47:1070-6 (2008)
DOI:10.1086/592072
Related
pathway
sdv00405  Phenazine biosynthesis
sdv02040  Flagellar assembly
KO pathway
ko02024   
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