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Search for "Pseudomonas aeruginosa" in Full Text gives 57 result(s) in Beilstein Journal of Organic Chemistry.

Efficient synthesis of phenylene-ethynylene rods and their use as rigid spacers in divalent inhibitors

  • Francesca Pertici,
  • Norbert Varga,
  • Arnoud van Duijn,
  • Matias Rey-Carrizo,
  • Anna Bernardi and
  • Roland J. Pieters

Beilstein J. Org. Chem. 2013, 9, 215–222, doi:10.3762/bjoc.9.25

Graphical Abstract
  • phenylene units. Preliminary applications of these rods in divalent systems are shown. Inhibition studies with Pseudomonas Aeruginosa lectin LecA showed that the rigid spacer proved greatly beneficial for the inhibitory potency. Keywords: multivalent carbohydrates; LecA inhibition; phenylene ethynylene
  • of aromatic rings. One of the spacers was incorporated into the structure of a divalent galactoside ligand and was used to inhibit the virulence-linked lectin LecA of Pseudomonas aeruginosa [27][28]. Results and Discussion Synthetic strategies Depending on the number of units in the spacer, two
  • obtained after deprotection of the alkyne moieties with K2CO3. Preliminary application As part of our program on bacterial adhesion inhibition by multivalent carbohydrates, the bacterial lectin LecA, a virulence factor of the problematic pathogen Pseudomonas aeruginosa is a target of interest [30][31
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Published 31 Jan 2013

Modulating the activity of short arginine-tryptophan containing antibacterial peptides with N-terminal metallocenoyl groups

  • H. Bauke Albada,
  • Alina-Iulia Chiriac,
  • Michaela Wenzel,
  • Maya Penkova,
  • Julia E. Bandow,
  • Hans-Georg Sahl and
  • Nils Metzler-Nolte

Beilstein J. Org. Chem. 2012, 8, 1753–1764, doi:10.3762/bjoc.8.200

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  • pathogens. Even if differences can be seen in the Gram-negative values, none of the RW-peptides was very active. Unfortunately, none of the peptides showed significant activity against Pseudomonas aeruginosa, a prominent pathogen that causes infections in e.g., cystic fibrosis patients. However, activities
  • in Table 2) The minimal inhibitory concentrations (MIC) were tested against Escherichia coli DSM 30083, Acinetobacter baumannii DSM 30007, Pseudomonas aeruginosa DSM 50071, Bacillus subtilis DSM 402, Staphylococcus aureus DSM 20231 (type strain), and Staphylococcus aureus ATCC 43300 (MRSA) in a
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Published 15 Oct 2012

Partial thioamide scan on the lipopeptaibiotic trichogin GA IV. Effects on folding and bioactivity

  • Marta De Zotti,
  • Barbara Biondi,
  • Cristina Peggion,
  • Matteo De Poli,
  • Haleh Fathi,
  • Simona Oancea,
  • Claudio Toniolo and
  • Fernando Formaggio

Beilstein J. Org. Chem. 2012, 8, 1161–1171, doi:10.3762/bjoc.8.129

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  • , Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Klebsiella pneumoniae ATCC 13883, Salmonella entereditis 13076, and Proteus mirabilis ATCC 10975. The well-known antibiotics bacitracin and tetracyclin (10 μg/disk) were used as controls. List of primary structures and abbreviations for the
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Published 24 Jul 2012

Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics

  • Marco Marradi,
  • Stefano Cicchi,
  • Francesco Sansone,
  • Alessandro Casnati and
  • Andrea Goti

Beilstein J. Org. Chem. 2012, 8, 951–957, doi:10.3762/bjoc.8.107

Graphical Abstract
  • enhance the avidity of interactions between glycans and lectins [15]. Some glycocalixarenes have shown remarkable inhibition properties towards galectins [21][22] or Pseudomonas Aeruginosa lectin [23], the inhibition ability being dependent on the macrocyclic conformation and presentation of the glycoside
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Published 26 Jun 2012

Synthetic glycopeptides and glycoproteins with applications in biological research

  • Ulrika Westerlind

Beilstein J. Org. Chem. 2012, 8, 804–818, doi:10.3762/bjoc.8.90

Graphical Abstract
  • distance (Figure 2) [140][141][142]. In another study, a combinatorial library of fucosyl-peptide dendrimers was synthesized and screened for binding to the fucose-specific lectin (LecB) from Pseudomonas aeruginosa, a pathogen causing severe infections in patients leading to chronic inflammation in the
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Published 30 May 2012

Mutational analysis of a phenazine biosynthetic gene cluster in Streptomyces anulatus 9663

  • Orwah Saleh,
  • Katrin Flinspach,
  • Lucia Westrich,
  • Andreas Kulik,
  • Bertolt Gust,
  • Hans-Peter Fiedler and
  • Lutz Heide

Beilstein J. Org. Chem. 2012, 8, 501–513, doi:10.3762/bjoc.8.57

Graphical Abstract
  • the center of the endophenazine cluster In between the mevalonate pathway genes and the dihydro-PCA biosynthesis genes, four further genes are situated, i.e., ppzTUVM (Figure 1). The gene ppzM (1023 bp) shows similarities to PhzM from Pseudomonas aeruginosa PAO1, a putative phenazine-specific
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Published 04 Apr 2012

Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues

  • Lucie Brulikova and
  • Jan Hlavac

Beilstein J. Org. Chem. 2011, 7, 678–698, doi:10.3762/bjoc.7.80

Graphical Abstract
  • tested for their antimicrobial activity against standard reference gram-positive and gram-negative bacterial strains such as Enterococcus faecalis CCM 4224, Staphylococcus aureus CCM 3953, Escherichia coli CCM 3954 and Pseudomonas aeruginosa CCM 3955 and against gram-positive and gram-negative bacteria
  • obtained from clinical material of patients treated at the University Hospital in Olomouc (methicillin resistant Staphylococcus aureus - MRSA, Staphylococcus haemolyticus, Escherichia coli and Pseudomonas aeruginosa) with resistance to currently used fluoroquinolones. Only the octyl and nonyl derivatives
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Published 26 May 2011
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