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N-Acyl
homoserine lactones (ASLs) as general signaling components of
Gram negatives bacteria
When Nealson et al. (1) and Eberhard (2)
first described the cell density phenomenon of bioluminescence in bacteria
and later identified the signaling component N-(3-oxohexanoyl) homoserine
lactone (3), nobody could foresee that the
family of N-Acyl homoserine lactones (ASL) seem to be an almost universal
signal factor in Gram negatives. When more bacteria producing ASLs became
known it seemed that these were often pathogens to animals and men,
as well as to plants. AHLs are produced e.g. by various opportunistic
pathogens such as Pseudomonas species or phyto-pathogens like Erwinia
species, or specific symbiotic strains as e.g. Rhizobium
species (for recent reviews see 47).
In these organisms AHLs induce the synthesis of compounds interacting
with the host organism, such as toxins, antibiotics or exoenzymes. However,
the observation that N-acyl homoserine lactones are also formed by certain
plankton phototrophic bacteria (8) indicated
that the phenomenon was of a more general nature. Furthermore, AHLs
have been found recently in natural microbial habitats, e.g. biofilms
(9), microbial mats and algal blooms (10).
The term "quorum sensing" is now used to describe a general
cell density dependent population response.
Mechanism
of ASL production
The AHLs known so far are the product of a luxI type gene (AHL synthase)
for the induction of bacterial species specific reactions. AHLs formed
by luxI bind to the product of the adjacent luxR gene; this activates
the transcription of genes responsible for the species specific response,
e.g. in Photo-bacterium fischeri the synthesis of the enzymes for bioluminescence.
All these responses seem to be related so far to the secondary metabolism.
Outlook: the potential role of ASLs
A variety of seemingly phylogenetically unrelated bacteria produce the
same AHL, other bacteria form more than one AHL. How these compounds
inter-play in natural habitats is still completely unknown. Bacterial
intercellular communication may be the basis for the expression of multiple
virulence determinants thus interfering with signal transduction and
may become a new tool to treat human, animal and plant infections (11).
Signaling compounds seem to be important in biofilm formation (12)
and exopolymer synthesis; interaction with the function of the AHL could
open new ways in technical processes where biofilms cause damage by
corrosion and biofouling.
Flukas contribution to quorum sensing research
We are pleased to announce the introduction of six important N-Acyl
homoserine lactones for quorum sensing research. The fact that these
important tools are now easily available will support significantly
your research. Additional ASLs will be added to our product range
later.
| Catalog No. |
Product
Name
|
Add to Cart |
|
09945
|
N-Butyryl-DL-homoserine lactone
BioChemika 25 mg |
|
|
09926
|
N-Hexanoyl-DL-homoserine lactone
BioChemika 25 mg |
|
|
10939
|
N-Heptanoyl-DL-homoserine lactone
BioChemika 25 mg |
|
|
10940
|
N-Octanoyl-DL-homoserine lactone
BioChemika 25 mg |
|
|
10937
|
N-Tetradecanoyl-DL-homoserine lactone
BioChemika 25 mg |
|
|
17248
|
N-Decanoyl-DL-homoserine lactone
BioChemika 25 mg |
|
|
17247
|
N-Dodecanoyl-DL-homoserine
BioChemika 25 mg |
|
|
10942
|
N-Butyryl-DL-homocysteine thiolactone
BioChemika 25 mg |
|
|
K3255
|
N-(beta-Ketocaproyl)-DL-homoserine lactone
(3-Oxo-hexanoyl-DL-homoserine lactone) 25 mg, 50mg |
|
|
O1764
|
N-(3-Oxooctanoyl)-L-homoserine lactone |
|
|
K3007
|
N-(β-Ketocaproyl)-L-homoserine lactone |
|
|
References:
- K.H. Nealson et al., J. Bacteriol. 104, 313322 (1970)
- A. Eberhard, J. Bacteriol. 109, 11011105 (1972)
- A. Eberhard et al., Biochemistry 20, 24442449 (1981)
- S. Swift et al., Trends Microbiol. 2, 193198 (1994)
- S. Swift et al., Trends in Biochem. 21, 214219 (1996)
- P.V. Dunlap, In: Bacteria as multicellular organisms, Oxford
University Press, Oxford, pp. 69106 (1997)
- S. Swift et al., In: Molecular Microbiology Springer, Berlin,
pp. 185207 (1998)
- A. Puskas et al., J. Bact. 179, 75307537 (1997)
- R.J.C. McLean et al., FEMS Microbiol. Lett. 154, 259263
(1997)
- R. Bachofen and A. Schenk, Microbiol. Res. 153, 6163
(1998)
- N.D. Robson et al., TibTech 15, 458464 (1997)
- D.G. Davies et al., Science 280, 295 298 (1998)
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