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1.
J Am Chem Soc ; 133(15): 5966-75, 2011 Apr 20.
Article in English | MEDLINE | ID: mdl-21434644

ABSTRACT

This manuscript describes the fabrication of arrays of spatially confined chambers embossed in a layer of poly(ethylene glycol) diacrylate (PEGDA) and their application to studying quorum sensing between communities of Pseudomonas aeruginosa. We hypothesized that biofilms may produce stable chemical signaling gradients in close proximity to surfaces, which influence the growth and development of nearby microcolonies into biofilms. To test this hypothesis, we embossed a layer of PEGDA with 1.5-mm wide chambers in which P. aeruginosa biofilms grew, secreted homoserine lactones (HSLs, small molecule regulators of quorum sensing), and formed spatial and temporal gradients of these compounds. In static growth conditions (i.e., no flow), nascent biofilms secreted N-(3-oxododecanoyl) HSL that formed a gradient in the hydrogel and was detected by P. aeruginosa cells that were ≤8 mm away. Diffusing HSLs increased the growth rate of cells in communities that were <3 mm away from the biofilm, where the concentration of HSL was >1 µM, and had little effect on communities farther away. The HSL gradient had no observable influence on biofilm structure. Surprisingly, 0.1-10 µM of N-(3-oxododecanoyl) HSL had no effect on cell growth in liquid culture. The results suggest that the secretion of HSLs from a biofilm enhances the growth of neighboring cells in contact with surfaces into communities and may influence their composition, organization, and diversity.


Subject(s)
Pseudomonas aeruginosa/physiology , Quorum Sensing , 4-Butyrolactone/analogs & derivatives , 4-Butyrolactone/metabolism , Biofilms/growth & development , Hydrogels/metabolism , Polyethylene Glycols/metabolism , Pseudomonas aeruginosa/growth & development
2.
Appl Environ Microbiol ; 76(4): 1241-50, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20023074

ABSTRACT

This paper describes a new approach for labeling intact flagella using the biarsenical dyes FlAsH and ReAsH and imaging their spatial and temporal dynamics on live Escherichia coli cells in swarming communities of bacteria by using epifluorescence microscopy. Using this approach, we observed that (i) bundles of flagella on swarmer cells remain cohesive during frequent collisions with neighboring cells, (ii) flagella on nonmotile swarmer cells at the leading edge of the colony protrude in the direction of the uncolonized agar surface and are actively rotated in a thin layer of fluid that extends outward from the colony, and (iii) flagella form transient interactions with the flagella of other swarmer cells that are in close proximity. This approach opens a window for observing the dynamics of cells in communities that are relevant to ecology, industry, and biomedicine.


Subject(s)
Arsenicals , Escherichia coli/physiology , Escherichia coli/ultrastructure , Flagella/physiology , Flagella/ultrastructure , Fluorescent Dyes , Base Sequence , Binding Sites/genetics , Biophysical Phenomena , DNA Primers/genetics , DNA, Bacterial/genetics , Ecosystem , Escherichia coli/genetics , Flagella/genetics , Genes, Bacterial , Genetic Engineering , Microscopy, Fluorescence , Movement/physiology , Recombination, Genetic
3.
Org Lett ; 8(11): 2357-60, 2006 May 25.
Article in English | MEDLINE | ID: mdl-16706525

ABSTRACT

[reaction: see text] We report the development of a safety-catch photolabile linker that allows the light-directed synthesis and spatially selective photorelease of oligonucleotides from microarrays. The linker remains stable to light during DNA synthesis, and is activated for photorelease after acidic hydrolysis. We demonstrate that the photoreleased oligonucleotides can be amplified by PCR to produce double stranded DNA. The advantages offered by this linker could aid the development of an automated gene synthesis platform.


Subject(s)
DNA/chemical synthesis , Oligonucleotides/chemical synthesis , Photolysis , DNA/chemistry , Molecular Structure , Oligonucleotides/chemistry
4.
J Am Chem Soc ; 126(51): 16704-5, 2004 Dec 29.
Article in English | MEDLINE | ID: mdl-15612691

ABSTRACT

We describe the development of photolabile protecting groups based on the 3,4,5-trimethoxyphenacyl group (TMP). Orthogonal safety-catches were created by introducing an acid-activatible dimethyl ketal (AA-TMP) and an oxidatively activatible 1,3-dithiane (OA-TMP) into the photolabile TMP group. We demonstrate the application of these protecting groups in light-directed synthesis of small molecule microarrays with diversity elements radially attached to a hydroxyproline scaffold.


Subject(s)
Acetophenones/chemistry , Combinatorial Chemistry Techniques/methods , Microarray Analysis/methods , Benzoin/chemistry , Hydroxyproline/chemistry , Photolysis
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