Autoinducer-2

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Autoinducer-2
Autoinducer-2
Names
Preferred IUPAC name
(3aS,6S,6aR)-2,2,6,6a-Tetrahydroxy-3a-methyltetrahydro-2H-furo[2,3-d][1,3,2]dioxaborol-2-uide
Other names
Dihydroxy[(2S,3R,4S)-2-methyldihydro-
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
  • InChI=1S/C5H10BO7/c1-4-5(8,3(7)2-11-4)13-6(9,10)12-4/h3,7-10H,2H2,1H3/q-1/t3-,4+,5+/m0/s1 checkY
    Key: ACKRRKSNOOISSG-VPENINKCSA-N checkY
  • InChI=1/C5H10BO7/c1-4-5(8,3(7)2-11-4)13-6(9,10)12-4/h3,7-10H,2H2,1H3/q-1/t3-,4+,5+/m0/s1
    Key: ACKRRKSNOOISSG-VPENINKCBL
  • O[C@@H]1[C@]2(O[B-](O[C@]2(OC1)C)(O)O)O
Properties
C5H10BO7
Molar mass 192.940
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Autoinducer-2 (AI-2), a furanosyl borate diester or tetrahydroxy furan (species dependent), is a member of a family of signaling molecules used in quorum sensing.[1] AI-2 is one of only a few known biomolecules incorporating boron. First identified in the marine bacterium Vibrio harveyi, AI-2 is produced and recognized by many Gram-negative and Gram-positive bacteria.[2][3] AI-2 arises by the reaction of 4,5-dihydroxy-2,3-pentanedione, which is produced enzymatically, with boric acid[4] and is recognized by the two-component sensor kinase LuxPQ in Vibrionaceae.

AI-2 is actively transported by the Lsr ABC-type transporter into the cell in Enterobacteriaceae and few other bacterial taxa such as Pasteurella, Photorhabdus, Haemophilus, and Bacillus,[5] where it is phosphorylated by LsrK. Then, Phospho-AI-2 binds the transcriptional repressor protein, LsrR, which subsequently is released from the promoter/operator region of the lsr operon – and transcription of the lsr genes is initiated. AI-2 signalling is also regulated by glucose and cAMP/CRP via the lsr operon. In the presence of glucose, low levels of cAMP/CRP result in almost no lsr operon (lsrABCDFG) expression. Without glucose, cAMP-CRP is needed to stimulate the lsr expression, while LsrR represses its expression in the absence of the inducer, phospho-AI-2. As AI-2 accumulates, more AI-2 is taken in via LsrABCD, phosphorylated via LsrK, and the lsr transcription is de-repressed, enabling even more AI-2 uptake.[6]

Doubts have been expressed regarding AI-2's status as a universal signal. Although the luxS gene, which encodes the protein responsible for AI-2 production is widespread, the latter has mainly a primary metabolic role in the recycling of S-adenosyl-L-methionine, with AI-2 being a by-product of that process.[7] An unequivocally AI-2 related behavior was found to be restricted primarily to organisms bearing known AI-2 receptor genes.[8] Thus, while it is certainly true that some bacteria respond to AI-2, it is doubtful that it is always being produced for purposes of signaling.

References[edit]

  1. ^ Cao, Jie-Gang; Meighen, Edward A. (1989). "Purification and structural identification of an autoinducer for the luminescence system of Vibrio harveyi". Journal of Biological Chemistry. 264 (36): 21670–21676. doi:10.1016/S0021-9258(20)88238-6. PMID 2600086.
  2. ^ Miller, Stephen T.; Xavier, Karina B.; Campagna, Shawn R.; Taga, Michiko E.; Semmelhack, Martin F.; Bassler, Bonnie L.; Hughson, Frederick M. (2004). "Salmonella typhimurium Recognizes a Chemically Distinct Form of the Bacterial Quorum-Sensing Signal AI-2". Molecular Cell. 15 (5): 677–687. doi:10.1016/j.molcel.2004.07.020. PMID 15350213.
  3. ^ Miller, M. B.; Bassler, B. L. (2001). "Quorum sensing in bacteria". Annual Review of Microbiology. 55: 165–199. doi:10.1146/annurev.micro.55.1.165. PMID 11544353.
  4. ^ "Chemistry - Queen Mary University of London".
  5. ^ Rezzonico, F.; Smits, T.H.M.; Duffy, B. (2012). "Detection of AI-2 receptors in genomes of Enterobacteriaceae suggests a role of type-2 quorum sensing in closed ecosystems". Sensors. 12 (5): 6645–6665. Bibcode:2012Senso..12.6645R. doi:10.3390/s120506645. PMC 3386761. PMID 22778662.
  6. ^ Wang, Liang; Hashimoto, Yoshifumi; Tsao, Chen-Yu; Valdes, James J.; Bentley, William E. (2005). "Cyclic AMP (cAMP) and cAMP Receptor Protein Influence both Synthesis and Uptake of Extracellular Autoinducer 2 in Escherichia coli". Journal of Bacteriology. 187 (6): 2066–2076. doi:10.1128/JB.187.6.2066-2076.2005. PMC 1064054. PMID 15743955.
  7. ^ Diggle, S. P.; Gardner, A.; West, S. A.; Griffin, A. S. (2007). "Evolutionary theory of bacterial quorum sensing: when is a signal not a signal?". Philosophical Transactions of the Royal Society B: Biological Sciences. 362 (1483): 1241–1249. doi:10.1098/rstb.2007.2049. PMC 2435587. PMID 17360270.
  8. ^ Rezzonico, F.; Duffy, B. (2008). "Lack of genomic evidence of AI-2 receptors suggests a non-quorum sensing role for luxS in most bacteria". BMC Microbiology. 8: 154. doi:10.1186/1471-2180-8-154. PMC 2561040. PMID 18803868.
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