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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-furodioxaborol-2-uide
Other names Dihydroxy[(2S,3R,4S)-2-methyldihydro-
Identifiers
3D model (JSmol)
Abbreviations AI-2
ChEBI
ChEMBL
ChemSpider
KEGG
PubChem CID
CompTox Dashboard (EPA)
InChI
  • 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/s1Key: ACKRRKSNOOISSG-VPENINKCSA-N
  • 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/s1Key: ACKRRKSNOOISSG-VPENINKCBL
SMILES
  • O12(O(O2(OC1)C)(O)O)O
Properties
Chemical formula C5H10BO7
Molar mass 192.940
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Autoinducer-2 (AI-2) is a furanosyl borate diester or tetrahydroxy furan (species dependent) that—as the name suggests—is an autoinducer, a member of a family of signaling molecules used in quorum sensing. 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. AI-2 arises by the reaction of 4,5-dihydroxy-2,3-pentanedione, which is produced enzymatically, with boric acid 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, 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.

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. An unequivocally AI-2 related behavior was found to be restricted primarily to organisms bearing known AI-2 receptor genes. 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.

Mimicry by host cells

It has been found that in response to bacteria or to disruption of the tight junction, mammalian epithelial cells synthesize an AI-2 mimic that triggers quorum sensing and may play an important role in enlisting gut microbes that are known to assist in epithelial healing. In reporting these findings, the researchers write that their results “suggest that crosskingdom communication occurs between eukaryotic cells and bacteria via the AI-2 bacterial quorum-sensing system.”

References

  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.
  9. Ismail, Anisa S.; Valastyan, Julie S.; Bassler, Bonnie L. (March 17, 2016). "A Host-Produced Autoinducer-2 Mimic Activates Bacterial Quorum Sensing". Cell Host & Microbe. 19 (4): 470–480. doi:10.1016/j.chom.2016.02.020. PMC 4869860. PMID 26996306.
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