ABSTRACT
A new synthetic route for the quorum sensing signal Autoinducer-2 (AI-2) is described and used for the preparation of [4-13C]-AI-2 starting from [1-13C]-bromoacetic acid. The key step in this process was the enantioselective reduction of an intermediate ketone. This synthesis provides, selectively, both enantiomers of the labelled or unlabelled parent compound, (R) or (S)-4,5-dihydroxypentane-2,3-dione (DPD) and was used for an improved synthesis of [1-13C]-AI-2.
Subject(s)
Homoserine/analogs & derivatives , Lactones/chemical synthesis , Lactones/pharmacology , Optical Phenomena , Quorum Sensing , Cyclization , Homoserine/chemical synthesis , Homoserine/pharmacology , Quorum Sensing/drug effectsABSTRACT
In processes regulated by quorum sensing (QS) bacteria respond to the concentration of autoinducers in the environment to engage in group behaviours. Autoinducer-2 (AI-2) is unique as it can foster interspecies communication. Currently, two AI-2 receptors are known, LuxP and LsrB, but bacteria lacking these receptors can also respond to AI-2. In this work, we present an efficient and reproducible synthesis of a novel chemical probe, d-desthiobiotin-AI-2. This probe binds both LuxP and LsrB receptors from different species of bacteria. Thus, this probe is able to bind receptors that recognise the two known biologically active forms of AI-2, presenting the plasticity essential for the identification of novel unknown AI-2 receptors. Moreover, a protocol to pull down receptors bound to d-desthiobiotin-AI-2 with anti-biotin antibodies has also been established. Altogether, this work highlights the potential of conjugating chemical signals to biotinylated derivatives to identify and tag signal receptors involved in quorum sensing or other chemical signalling processes.
Subject(s)
Biotin/analogs & derivatives , Escherichia coli Proteins/metabolism , Homoserine/analogs & derivatives , Lactones/chemical synthesis , Quorum Sensing/drug effects , Alkynes/chemistry , Biotin/chemical synthesis , Biotin/chemistry , Biotin/metabolism , Carrier Proteins/metabolism , Escherichia coli/genetics , Homoserine/chemical synthesis , Homoserine/metabolism , Lactones/metabolism , Ligands , Molecular Structure , Signal TransductionABSTRACT
In this study, we have investigated the effects of the newly synthesized analog of Pseudomonas aeruginosa quorum-sensing autoinducer named AIA-1 (autoinducer analog) against antibiotic-resistant bacteria. In vitro susceptibility and killing assays for P. aeruginosa PAO1ΔoprD mutant and clinical isolates were performed by using antibiotics and AIA-1. In an in vivo assay, a luminescent carbapenem-resistant strain derived from PAO1ΔoprD was injected into neutropenic ICR mice and bioluminescence images were acquired after the treatment with antibiotics and AIA-1. Additionally, we investigated the effects of the combination use against carbapenem-resistant Enterobacteriaceae (CRE). Using killing assays in P. aeruginosa, the survival rates in the presence of antibiotics and AIA-1 significantly decreased in comparison with those with antibiotics alone. Furthermore, dual treatment of biapenem and AIA-1 was more effective than biapenem alone in a mouse infection model. AIA-1 did not change the MICs in P. aeruginosa, suggesting that AIA-1 acts on the mechanism of antibiotic tolerance. Conversely, the MICs of antibiotics decreased in the presence of AIA-1 in some CRE strains, indicating that AIA-1 may require additional mechanism to act on CRE. In conclusion, AIA-1 may be a potent drug for clinical treatment of infections caused by antibiotic-resistant bacteria. J. Med. Invest. 64: 101-109, February, 2017.
Subject(s)
Anti-Bacterial Agents/administration & dosage , Homoserine/analogs & derivatives , Lactones/administration & dosage , Pseudomonas aeruginosa/drug effects , Animals , Carbapenems/pharmacology , Drug Synergism , Homoserine/administration & dosage , Homoserine/chemical synthesis , Homoserine/chemistry , Humans , Lactones/chemical synthesis , Lactones/chemistry , Mice , Mice, Inbred ICR , Pseudomonas Infections/drug therapy , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/genetics , Quorum Sensing/drug effects , Thienamycins/administration & dosage , beta-Lactam ResistanceABSTRACT
Indospicine is a non-proteogenic amino acid that accumulates as the free amino acid in livestock grazing Indigofera plant species and causes both reproductive losses and hepatotoxic effects. An efficient synthetic route to l-indospicine from l-homoserine lactone is described. The methodology is applicable for the synthesis of both deuterium labelled isotopomers and structural analogues for utilisation in biological studies. The key steps are a zinc mediated Barbier reaction with acrylonitrile and a Pinner reaction that together introduce the target amidine moiety.
Subject(s)
Indigofera/chemistry , Norleucine/analogs & derivatives , Acrylonitrile/chemical synthesis , Acrylonitrile/chemistry , Copper/chemistry , Homoserine/chemical synthesis , Homoserine/chemistry , Lactones/chemical synthesis , Lactones/chemistry , Norleucine/chemical synthesis , Norleucine/chemistry , Zinc/chemistryABSTRACT
Starting from chiral-protected 4-hydroxymethyl pyrrolidin-2-ones, the otherwise elusive 3,4-trans-3,3,4-trisubstituted isosteres of α-methyl homoserine, tethered on a γ-lactam ring, were prepared exploiting stereoselective electrophilic aminations. These reactions led to the isolation and characterization of a novel type of atropisomers, exceedingly stable at room temperature, that were directly converted to the desired products by a novel non-reductive N-N bond cleavage reaction.
Subject(s)
Homoserine/analogs & derivatives , Homoserine/chemical synthesis , Lactams/chemistry , Amination , Homoserine/chemistry , Molecular Conformation , Molecular Structure , StereoisomerismABSTRACT
We disclose here the synthesis of a series of macrocyclic HCV protease inhibitors, where the homoserine linked together the quinoline P2' motif and the macrocyclic moiety. These compounds exhibit potent inhibitory activity against HCV NS3/4A protease and replicon cell based assay. Their enzymatic and antiviral activities are modulated by substitutions on the quinoline P2' at position 8 by methyl and halogens and by small heterocycles at position 2. The in vitro structure activity relationship (SAR) studies and in vivo pharmacokinetic (PK) evaluations of selected compounds are described herein.
Subject(s)
Antiviral Agents/chemical synthesis , Antiviral Agents/pharmacology , Hepacivirus/drug effects , Homoserine/pharmacology , Serine Proteinase Inhibitors/chemical synthesis , Serine Proteinase Inhibitors/pharmacology , Viral Nonstructural Proteins/antagonists & inhibitors , Antiviral Agents/chemistry , Dose-Response Relationship, Drug , Hepacivirus/enzymology , Homoserine/chemical synthesis , Homoserine/chemistry , Microbial Sensitivity Tests , Molecular Structure , Serine Proteinase Inhibitors/chemistry , Structure-Activity Relationship , Viral Nonstructural Proteins/metabolismABSTRACT
Autoinducer-2 (AI-2) has been suggested to serve as a ubiquitous quorum sensing (QS) signal that mediates intra- and interspecies cross-talk between bacteria. To add tools for the study of its function in bacterial communication, we present a new and an improved synthetic route to AI-2 and aromatic analogues. We used this strategy to prepare naphthyl-DPD, and observed remarkably high synergistic activity at low nanomolar concentrations for this analogue in Vibrio harveyi.
Subject(s)
Homoserine/analogs & derivatives , Lactones/pharmacology , Quorum Sensing/drug effects , Vibrio/drug effects , Homoserine/chemical synthesis , Homoserine/chemistry , Homoserine/metabolism , Homoserine/pharmacology , Lactones/chemical synthesis , Lactones/chemistry , Lactones/metabolism , Molecular Structure , Vibrio/metabolismABSTRACT
We report methods for the synthesis of polypeptides that are fully functionalized with desirable phosphorylcholine, PC, groups. Because of the inherent challenges in the direct incorporation of the PC group into α-amino acid N-carboxyanhydride (NCA) monomers, we developed a synthetic approach that combined functional NCA polymerization with efficient postpolymerization modification. While poly(L-phosphorylcholine serine) was found to be unstable upon synthesis, we successfully prepared poly(L-phosphorylcholine homoserine) with controlled chain lengths and found these to be water-soluble with disordered chain conformations.
Subject(s)
Homoserine/analogs & derivatives , Peptides/chemical synthesis , Phosphorylcholine/analogs & derivatives , Serine/analogs & derivatives , Homoserine/chemical synthesis , Peptides/chemistry , Phosphorylcholine/chemical synthesis , Polymerization , Serine/chemical synthesisABSTRACT
The straightforward syntheses of enantiopure (2R)-2-trifluoromethyl-2-carboxyazetidine and (R)- and (S)-trifluoromethylhomoserines are reported. The key step is a Strecker-type reaction on a common chiral CF3-containing bicyclic oxazolidine intermediate obtained by a condensation reaction of (R)-phenylglycinol and ethyl-4,4,4-trifluoroacetoacetate (ETFAA).
Subject(s)
Acetoacetates/chemistry , Amino Alcohols/chemical synthesis , Azetidinecarboxylic Acid/chemical synthesis , Azetidines/chemical synthesis , Homoserine/chemical synthesis , Amino Alcohols/chemistry , Azetidinecarboxylic Acid/chemistry , Azetidines/chemistry , Catalysis , Homoserine/chemistry , Molecular Structure , Oxazoles/chemistry , StereoisomerismABSTRACT
Starting from a chiral 4-hydroxymethyl pyrrolidin-2-one, an isostere of α-methyl homoserine tethered on a γ-lactam ring was prepared exploiting a stereoselective acylation-methylation sequence, followed by Curtius rearrangement, and structural assignment was confirmed by n.O.e. experiments. By reverting the sequence, the 3-carboxy-3-methyl derivative having the opposite configuration at C-3 was obtained with total stereoselection, but Curtius rearrangement invariably afforded only inseparable mixtures of decomposition products.
Subject(s)
Homoserine/chemistry , Lactams/chemistry , Peptides, Cyclic/chemical synthesis , Acylation , Alkylation , Homoserine/chemical synthesis , Methylation , Molecular Structure , Peptides, Cyclic/chemistry , StereoisomerismABSTRACT
The primary quorum sensing system in the opportunistic pathogen Pseudomonas aeruginosa is regulated through the synthesis and secretion of N-3-oxo-dodecanoyl-L-homoserine lactone (C12) which binds the transcriptional activator LasR. In this study we report the design, synthesis and biological evaluation of new analogs of C12. Analysis of the autoinducer binding site cavity of LasR revealed a positively charged cavity near the center of bound C12. Accordingly, we synthesized two piperidine-C12 diastereoisomers and tested their biological activity. Both analogs proved to be strong LasR agonists that showed a synergistic effect when presented together with the natural ligand. Moreover, binding of the analogs resulted in phenotypic changes characteristic of QS controlled receptor activation.
Subject(s)
4-Butyrolactone/analogs & derivatives , Bacterial Proteins/agonists , Homoserine/analogs & derivatives , Pseudomonas aeruginosa/drug effects , Quorum Sensing/drug effects , Trans-Activators/agonists , 4-Butyrolactone/chemical synthesis , 4-Butyrolactone/chemistry , 4-Butyrolactone/pharmacology , Dose-Response Relationship, Drug , Homoserine/chemical synthesis , Homoserine/chemistry , Homoserine/pharmacology , Models, Molecular , Molecular Dynamics Simulation , Molecular Structure , Structure-Activity RelationshipABSTRACT
Fluorine ((19)F) NMR is a valuable tool for studying dynamic biological processes. However, increasing the sensitivity of fluorinated reporter molecules is a key to reducing acquisition times and accessing transient biological interactions. Here, we evaluate the utility a novel amino acid, L-O-(perfluoro-t-butyl)-homoserine (pFtBSer), that can easily be synthesized and incorporated into peptides and provides greatly enhanced sensitivity over currently used (19)F biomolecular NMR probes. Incorporation of pFtBSer into the potent antimicrobial peptide MSI-78 results in a sharp (19)F NMR singlet that can be readily detected at concentrations of 5 µm and lower. We demonstrate that pFtBSer incorporation into MSI-78 provides a sensitive tool to study binding through (19)F NMR chemical shift and nuclear relaxation changes. These results establish future potential for pFtBSer to be incorporated into various proteins where NMR signal sensitivity is paramount, such as in-cell investigations.
Subject(s)
Fluorine/chemistry , Homoserine/chemical synthesis , Nuclear Magnetic Resonance, Biomolecular , Peptides/chemical synthesis , Circular Dichroism , Fluorocarbons/chemical synthesis , Fluorocarbons/chemistry , Homoserine/analogs & derivatives , Homoserine/chemistry , Humans , Indicators and Reagents/chemistry , Indicators and Reagents/isolation & purification , Peptides/chemistry , Peptides/isolation & purification , Protein Conformation , Solutions/chemistry , tert-Butyl Alcohol/analogs & derivatives , tert-Butyl Alcohol/chemical synthesis , tert-Butyl Alcohol/chemistryABSTRACT
As a guide for chemical probe design, focused analogue synthetic studies were undertaken upon the lactone ring of 3-oxo-C(12)-homoserine lactone. We have concluded that hydrolytic instability of the heterocyclic ring is pivotal for its ability to modulate immune signaling and probe preparation was aligned with these findings.
Subject(s)
4-Butyrolactone/analogs & derivatives , Homoserine/analogs & derivatives , Quorum Sensing/physiology , 4-Butyrolactone/chemical synthesis , 4-Butyrolactone/chemistry , 4-Butyrolactone/metabolism , Animals , Bone Marrow Cells/cytology , Endoplasmic Reticulum Stress , Homoserine/chemical synthesis , Homoserine/chemistry , Homoserine/metabolism , Immunomodulation , Macrophages/immunology , Macrophages/metabolism , Mice , NF-kappa B/metabolism , Oxidation-Reduction , Poly(ADP-ribose) Polymerases/metabolism , Pseudomonas aeruginosa/physiologyABSTRACT
Pseudomonas aeruginosa is a notorious human pathogen associated with a range of life-threatening nosocomial infections. There is an increasing problem of antibiotic resistance in P. aeruginosa, highlighted by the emergence of multi-drug resistant strains. Thus the exploration of new strategies for the treatment of P. aeruginosa infections is clearly warranted. P. aeruginosa is known to produce a range of virulence factors that enhance its ability to damage the host tissue and cause disease. One of the most important virulence factors is pyocyanin. P. aeruginosa regulates pyocyanin production using an intercellular communication mechanism called quorum sensing, which is mediated by small signalling molecules termed autoinducers. One native autoinducer is N-(3-oxododecanoyl)-L-homoserine lactone (OdDHL). Herein we report the synthesis of a collection of abiotic OdDHL-mimics. A number of novel compounds capable of competing with the endogenous OdDHL and consequently, inhibiting the production of pyocyanin in cultures of wild type P. aeruginosa were identified. We present evidence suggesting that compounds of this general structural type act as direct antagonists of quorum sensing in P. aeruginosa and as such may find value as molecular tools for the study and manipulation of this signalling pathway. A direct quantitative comparison of the pyocyanin suppressive activities of the most active OdDHL-mimics with some previously-reported inhibitors (based around different general structural frameworks) of quorum sensing from the literature, was also made.
Subject(s)
4-Butyrolactone/analogs & derivatives , Homoserine/analogs & derivatives , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/drug effects , Pyocyanine/metabolism , Quorum Sensing/drug effects , Virulence Factors/metabolism , 4-Butyrolactone/chemical synthesis , 4-Butyrolactone/chemistry , 4-Butyrolactone/pharmacology , Homoserine/chemical synthesis , Homoserine/chemistry , Homoserine/pharmacology , Humans , Pseudomonas Infections/drug therapy , Pseudomonas aeruginosa/metabolism , Pseudomonas aeruginosa/pathogenicity , Small Molecule Libraries/chemical synthesis , Small Molecule Libraries/chemistry , Small Molecule Libraries/pharmacologyABSTRACT
There have been intensive efforts to find small molecule antagonists for bacterial quorum sensing (QS) mediated by the "universal" QS autoinducer, AI-2. Previous work has shown that linear and branched acyl analogues of AI-2 can selectively modulate AI-2 signaling in bacteria. Additionally, LsrK-dependent phosphorylated analogues have been implicated as the active inhibitory form against AI-2 signaling. We used these observations to synthesize an expanded and diverse array of AI-2 analogues, which included aromatic as well as cyclic C-1-alkyl analogues. Species-specific analogues that disrupted AI-2 signaling in Escherichia coli and Salmonella typhimurium were identified. Similarly, analogues that disrupted QS behaviors in Pseudomonas aeruginosa were found. Moreover, we observed a strong correlation between LsrK-dependent phosphorylation of these acyl analogues and their ability to suppress QS. Significantly, we demonstrate that these analogues can selectively antagonize QS in single bacterial strains in a physiologically relevant polymicrobial culture.
Subject(s)
Escherichia coli/metabolism , Homoserine/analogs & derivatives , Lactones/chemistry , Lactones/metabolism , Pseudomonas aeruginosa/metabolism , Quorum Sensing , Salmonella typhimurium/metabolism , Escherichia coli/enzymology , Escherichia coli Proteins/metabolism , Homoserine/chemical synthesis , Homoserine/chemistry , Homoserine/metabolism , Lactones/chemical synthesis , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Repressor Proteins/metabolism , Salmonella typhimurium/enzymology , Signal Transduction , beta-Galactosidase/metabolismABSTRACT
Quorum sensing (QS) is a communication procedure that predominates gene expression in response to cell density and fluctuations in the neighboring environment as a result of discerning molecules termed autoinducers (AIs). It has been embroiled that QS can govern bacterial behaviors such as the secretion of virulence factors, biofilm formation, bioluminescence production, conjugation, sporulation and swarming motility. Autoinducer 2 (AI-2), a QS signaling molecule brought up to be involved in interspecies communication, exists in both gram-negative and -positive bacteria. Therefore, novel approaches to interrupt AI-2 quorum sensing are being recognized as next generation antimicrobials. In the present review article, we summarized recent progresses on AI-2 bacterial quorum sensing inhibitors and discussed their potential as the antibacterial agents.
Subject(s)
Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Bacteria/drug effects , Bacteria/metabolism , Bacterial Proteins/antagonists & inhibitors , Homoserine/analogs & derivatives , Lactones/chemistry , Quorum Sensing/drug effects , Anti-Bacterial Agents/chemical synthesis , Bacterial Proteins/metabolism , Carbon-Sulfur Lyases/antagonists & inhibitors , Carbon-Sulfur Lyases/metabolism , Carrier Proteins/antagonists & inhibitors , Carrier Proteins/metabolism , Escherichia coli Proteins/antagonists & inhibitors , Escherichia coli Proteins/metabolism , Homoserine/chemical synthesis , Homoserine/chemistry , Homoserine/pharmacology , Lactones/chemical synthesis , Lactones/pharmacology , N-Glycosyl Hydrolases/metabolism , Pentanes/chemical synthesis , Pentanes/chemistry , Pentanes/pharmacologyABSTRACT
Quorum sensing is defined as the ability of microorganisms to sense their population density via the release of signaling molecules composed of acyl-homoserine lactone (AHL), which is a type of autoinducer (AI). Previous structure-activity relationship (SAR) studies demonstrated that the 3-oxo group, homoserine lactone of L-form, and long acyl side chain have crucial roles in apoptosis induction. Various types of synthetic AI analogs of Pseudomonas aeruginosa were prepared, and SAR study was conducted to determine their effects against human oral squamous carcinoma cells derived from gingival carcinoma Ca9-22 cells and tongue cancer SAS cells. Not only the antiproliferative potential but also the radiation-sensitizing effects against these cells were examined. It was found that antiproliferative activity partly depended on HSL structure and acyl side chain length. Moreover, a few compounds, compound 5 and 87, showed antiproliferative effects against both Ca9-22 and SAS cells, and also induced radiation-sensitizing effects against Ca9-22 cells. Compound 5 alone induced apoptotic cell death accompanied by sub-G1 phase accumulation in cell cycle and caspase-3 activation, and radiation-sensitizing effects of compound 5 could be attributed to enhanced apoptosis induction. In contrast, there were no remarkable alterations in cell cycle distribution in Ca9-22 treated with compound 87 alone or in combination. However, both compounds lack 3-oxo and their acyl side chain lengths are not necessarily long. This SAR study demonstrated that HSL analogs, which lacked the recommended characteristics for apoptosis induction clearly showed antiproliferative and radiation-sensitizing activity in Ca9-22 cells.
Subject(s)
Acyl-Butyrolactones/pharmacology , Antineoplastic Agents/pharmacology , Carcinoma, Squamous Cell/pathology , Cell Proliferation/drug effects , Homoserine/analogs & derivatives , Lactones/pharmacology , Mouth Neoplasms/pathology , Pseudomonas aeruginosa/metabolism , Quorum Sensing , Radiation-Sensitizing Agents/pharmacology , Acyl-Butyrolactones/chemical synthesis , Antineoplastic Agents/chemical synthesis , Apoptosis/drug effects , Cell Cycle/drug effects , Cell Line, Tumor , Dose-Response Relationship, Drug , Dose-Response Relationship, Radiation , Homoserine/chemical synthesis , Homoserine/pharmacology , Humans , Inhibitory Concentration 50 , Lactones/chemical synthesis , Molecular Structure , Radiation-Sensitizing Agents/chemical synthesis , Structure-Activity Relationship , Time FactorsABSTRACT
Bacteria coordinate population-dependent behaviors such as virulence by intra- and inter-species communication (quorum sensing). Autoinducer-2 (AI-2) regulates inter-species quorum sensing. AI-2 derives from the spontaneous cyclisation of linear (S)-4,5-dihydroxypentanedione (DPD) into two isomeric forms in dynamic equilibrium. Different species of bacteria have different classes of AI-2 receptors (LsrB and LuxP) which bind to different cyclic forms. In the present work, DPD analogs with a new stereocenter at C-5 (4,5-dihydroxyhexanediones (DHDs)) have been synthesized and their biological activity tested in two bacteria. (4S,5R)-DHD is a synergistic agonist in Escherichia coli (which contains the LsrB receptor), while it is an agonist in Vibrio harveyi (LuxP), displaying the strongest agonistic activity reported so far (EC(50)=0.65µM) in this organism. Thus, modification at C-5 opens the way to novel methods to manipulate quorum sensing as a method for controlling bacteria.
Subject(s)
Escherichia coli/drug effects , Escherichia coli/metabolism , Homoserine/analogs & derivatives , Lactones/chemistry , Lactones/pharmacology , Quorum Sensing/drug effects , Vibrio/drug effects , Vibrio/metabolism , Bacterial Proteins/agonists , Bacterial Proteins/metabolism , Cyclization , Escherichia coli Proteins/agonists , Escherichia coli Proteins/metabolism , Hexanes/chemistry , Homoserine/chemical synthesis , Homoserine/chemistry , Homoserine/pharmacology , Lactones/chemical synthesis , Pentanes/chemistry , Repressor Proteins/agonists , Repressor Proteins/metabolism , StereoisomerismABSTRACT
Bacteria have developed a cell-to-cell communication system, termed quorum sensing (QS), which allows for the population-dependent coordination of their behavior via the exchange of chemical signals. Autoinducer-2 (AI-2), a class of QS signals derived from 4,5-dihydroxy-2,3-pentandione (DPD), has been revealed as a universal signaling molecule in a variety of bacterial species. In spite of considerable interest, the study of putative AI-2 based QS systems remains a challenging topic in part due to the rapid interconversion between the linear and cyclic forms of DPD. Herein, we report the design and development of efficient syntheses of carbocyclic analogues of DPD, which are locked in the cyclic form. The synthetic analogues were evaluated for the modulation of AI-2-based QS in Vibrio harveyi and Salmonella typhimurium. No agonists were uncovered in either V. harveyi or S. typhimurium assay, whereas weak to moderate antagonists were found against V. harveyi. On the basis of NMR analyses and DFT calculations, the heterocyclic oxygen atom within DPD appears necessary to promote hydration at the C3 position of cyclic DPD to afford the active tetrahydroxy species. These results also shed light on the interaction between the heterocyclic oxygen atom and receptor proteins as well as the importance of the linear form and dynamic equilibrium of DPD as crucial requirements for activation of AI-2 based QS circuits.
Subject(s)
Homoserine/analogs & derivatives , Lactones/chemistry , Quorum Sensing , Homoserine/chemical synthesis , Homoserine/chemistry , Lactones/chemical synthesis , Magnetic Resonance Spectroscopy , Molecular Structure , Pentanones/chemical synthesis , Pentanones/chemistry , Quantum Theory , Salmonella typhimurium/chemistry , Salmonella typhimurium/metabolism , Vibrio/chemistry , Vibrio/metabolismABSTRACT
The Pseudomonas aeruginosa quorum-sensing molecule N-(3-oxododecanoyl)-l-homoserine lactone (1) is involved not only in bacterial activation but also in subversion of the host immune system, and this compound might thus be used as a template to design immunosuppressive agents, provided derivatives devoid of quorum-sensing activity could be discovered. By use of a leukocyte proliferation assay and a newly developed bioluminescent P. aeruginosa reporter assay, systematic modification of 1 allowed us to delineate the bacterial LasR-induction and host immunosuppressive activities. The main determinant is replacement of the methylene group proximal to the ß-ketoamide in the acyl chain of 1 with functions containing heteroatoms, especially an NH group. This modification can be combined with replacement of the homoserine lactone system in 1 with stable cyclic groups. For example, we found the simple compound N(1)-(5-chloro-2-hydroxyphenyl)-N(3)-octylmalonamide (25d) to be over twice as potent as 1 as an immune suppressor while displaying LasR-induction antagonist activity.