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71.
Xiao Chen Katharina Buddrus-Schiemann Michael Rothballer Petra M. Kr?mer Anton Hartmann 《Analytical and bioanalytical chemistry》2010,398(6):2669-2676
The Burkholderia cepacia complex (Bcc) employs a quorum sensing (QS) mechanism which is a cell density-dependent bacterial communication system to
regulate certain gene expressions. As with many other Gram-negative bacteria, Burkholderia cepacia species use (N-acyl-)homoserine lactones (AHLs or HSLs) as signalling molecules. Because of the essential role of QS in bacterial behavior,
the aim of this study was to demonstrate the applicability of our in-house-developed enzyme-linked immunosorbent assays (ELISAs)
for the detection of bacterial activities via HSLs in B. cepacia strain LA3 culture supernatants. For this purpose the previously developed monoclonal antibodies (mAbs) HSL1/2-2C10 and HSL1/2-4H5
were exploited. N-3-Oxo-decanoyl-L-homoserine lactone (3-oxo-C10-HSL) was used as main analyte throughout all experiments. With the bacterial
culture medium (named ABC medium) a matrix effect in both ELISAs was visible (slight increase in optical density, shift in
test midpoints (IC50) and working ranges). For example, ELISA with mAb HSL1/2-2C10 and enzyme tracer HSL3-HRP (HSL derivative conjugated to horseradish
peroxidase) had an IC50 of 120 μg L−1 for 3-oxo-C10-HSL in phosphate-buffered saline versus 372 μg L−1 in ABC medium. A significant increase of HSLs in B. cepacia strain LA3 culture supernatants after 12 h to 48 h of growth was observed. Although the analytical result of these immunoassays
cannot distinguish HSLs from homoserines (HSs), the appearance of these compounds can be easily followed. Hydrolysis and spiking
experiments were carried out with these biological samples. According to our knowledge, these are the first immunoassays for
the detection of quorum sensing molecules in biological culture supernatants. This study provides a cost-effective, fast,
and sensitive analytical method for detection of HSLs/HSs in biological samples without complex sample preparation and will
offer a quick idea about B. cepacia activities. The low sample amount requirement (less than 1 mL) constitutes a tremendous advantage for many analytical questions
with biological samples. 相似文献
72.
73.
Schrade A Cao Z Landfester K Ziener U 《Langmuir : the ACS journal of surfaces and colloids》2011,27(11):6689-6700
Well-defined raspberry-like nanocapsules were prepared by the combination of Pickering emulsification and solvent displacement technique by using silica particles as stabilizer and hexadecane (HD) as soft template. The formation of the capsule morphology is caused by the phase separation of poly(styrene-co-4-vinyl pyridine) (poly(St-co-4-VP)) in the droplets due to the diffusion of good solvent for the (co)polymer to the aqueous continuous phase. The size of capsules was successfully reduced from tens of micrometers in the dispersion by simply stirring to the nanorange by the employment of sonication and Ostwald ripening. The formation of silica-particles-armored nanocapsules was confirmed by transmission electron microscopy (TEM), high-resolution scanning electron microscopy (HRSEM), dynamic light scattering (DLS), and zeta potential measurement. The colloidal stability and particle properties, including size and morphology, depend on the amount of HD, and copolymers, the sonication time, the dispersion pH value, the type of solvent, and the copolymer composition. 相似文献
74.
Katharina K. Strelau Thomas Schüler Dr. Robert Möller Dr. Wolfgang Fritzsche Dr. habil. Jürgen Popp Prof. Dr. 《Chemphyschem》2010,11(2):394-398
Surface‐enhanced Raman spectroscopy (SERS) is an emerging technology in the field of analytics. Due to the high sensitivity in connection with specific Raman molecular fingerprint information SERS can be used in a variety of analytical, bioanalytical, and biosensing applications. However, for the SERS effect substrates with metal nanostructures are needed. The broad application of this technology is greatly hampered by the lack of reliable and reproducible substrates. Usually the activity of a given substrate has to be determined by time‐consuming experiments such as calibration or ultramicroscopic studies. To use SERS as a standard analytical tool, cheap and reproducible substrates are required, preferably with a characterization technique that does not interfere with the subsequent measurements. Herein we introduce an innovative approach to produce low‐cost and large‐scale reproducible substrates for SERS applications, which allows easy and economical production of micropatterned SERS active surfaces on a large scale. This approach is based on an enzyme‐induced growth of silver nanostructures. The special structural feature of the enzymatically deposited silver nanoparticles prevents the breakdown of SERS activity even at high particle densities (particle density >60 %) that lead to a conductive layer. In contrast to other approaches, this substrate exhibits a relationship between electrical conductivity and the resulting SERS activity of a given spot. This enables the prediction of the SERS activity of the nanostructure ensemble and therewith the controllable and reproducible production of SERS substrates of enzymatic silver nanoparticles on a large scale, utilizing a simple measurement of the electrical conductivity. Furthermore, through a correlation between the conductivity and the SERS activity of the substrates it is possible to quantify SERS measurements with these substrates. 相似文献
75.
(NH4)2[Mo6Cl14] · H2O ( 1 ) was prepared from reactions of MoCl2 in ethanol with aqueous NH4Cl solution. It crystallizes in the monoclinic space group I2/a (no. 15), Z = 4 with a = 912.3(1), b = 1491.2(2), c = 1724.8(2) pm, β = 92.25(1)°; R1 = 0.023 (based on F values) and wR2 = 0.059 (based on F2 values), for all measured X‐ray reflections. The structure of the cluster anion can be given as [(Mo6Cl)Cl]2– (i = inner, a = outer ligands). Thermal stability studies show that 1 loses crystal water followed by the loss of NH4Cl above 350 °C to yield MoCl2. The water‐free compound (NH4)2[Mo6Cl14] ( 2 ) was synthesized by solid state reaction of MoCl2 and NH4Cl in a sealed quartz ampoule at 270 °C. No single‐crystals could be obtained. Decompositions of 1 and 2 under nitrogen and argon exhibited the loss of NH4Cl at about 350 °C. Decomposition under NH3 resulted in the formation of MoN and Mo2N at 540 °C and 720 °C, respectively. 相似文献
76.
77.
78.
Maria-Verena Kohnle Ulrich Ziener Katharina Landfester 《Colloid and polymer science》2009,287(3):259-268
High-butadiene-level styrene–butadiene rubber latexes up to high solid-contents are synthesized using the miniemulsion process.
It is shown that the miniemulsion polymerization approach offers an efficient heterophase route synthesizing styrene–butadiene
copolymer latexes with flexible copolymer composition and narrow size distribution of the resulting latex particles. Secondary
nucleation was successfully prevented by using a hydrophobic initiator. Due to the nanoreactor situation, even at high conversions,
a low crosslinking degree and, therefore, low gel contents are obtained. The microstructure of the polymers obtained in miniemulsion
is independent of the synthesis parameters, especially the temperature. The molecular weight can be easily adjusted by the
application of transfer agents while the insoluble gel content is substantially reduced. An up-scaling of the procedure is
easily possible. 相似文献
79.
Regioselective Ring‐Opening Polymerization of a Polyhydroxycarboxylic Acid for the Synthesis of a Nanoscale Carrier Material with pH‐Dependent Stability and Sustained Drug Release 下载免费PDF全文
Dipl.‐Chem. Alexander Ewe Dr. Anita Jansen de Salazar Dipl.‐Phys. Katharina Lemmnitzer Michael Marsch Prof. Dr. Achim Aigner Prof. Dr. Armin Geyer 《Angewandte Chemie (International ed. in English)》2015,54(21):6364-6369
Synthetic polyesters are usually composed of monohydroxycarboxylic acids to avoid the problem of regioselectivity during ring‐opening polymerization. In contrast, the linear polyester BICpoly contains four secondary OH groups and is nevertheless esterified regioselectively at only one of these positions. Neither the synthesis of the tricyclic monomers nor the ring‐opening polymerization requires protecting groups, making BICpoly an attractive novel and biocompatible polymer. BICpoly nanoparticles can be loaded with low‐molecular weight drugs or coated onto surfaces as thin films. The release of loaded compounds makes BICpoly an attractive depot for drug release, as shown herein by loading BICpoly with dyes or the cytostatic drug doxorubicin. BICpoly is distinguishable from other polymers by its characteristic pH‐dependent degradation. 相似文献
80.
M.Sc. Katharina Heller M.Sc. Philipp Ochtrop M.Sc. Michael F. Albers Florian B. Zauner Prof. Dr. Aymelt Itzen Prof. Dr. Christian Hedberg 《Angewandte Chemie (International ed. in English)》2015,54(35):10327-10330
We present a new protein labeling method based on the covalent enzymatic phosphocholination of a specific octapeptide amino acid sequence in intact proteins. The bacterial enzyme AnkX from Legionella pneumophila has been established to transfer functional phosphocholine moieties from synthetically produced CDP‐choline derivatives to N‐termini, C‐termini, and internal loop regions in proteins of interest. Furthermore, the covalent modification can be hydrolytically removed by the action of the Legionella enzyme Lem3. Only a short peptide sequence (eight amino acids) is required for efficient protein labeling and a small linker group (PEG‐phosphocholine) is introduced to attach the conjugated cargo. 相似文献