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Holger Kühn

Publications and source records attributed to Holger Kühn.

5 recordsLinked to original sources

Mobile high resolution xenon nuclear magnetic resonance spectroscopy in the earth's magnetic field.

Conventional high resolution nuclear magnetic resonance (NMR) spectra are usually measured in homogeneous, high magnetic fields (>1 T), which are produced by expensive and immobile superconducting magnets. We show that chemically resolved xenon (Xe) NMR spectroscopy of liquid samples can be measured in the Earth's magnetic field (5 x 10(-5) T) with a continuous flow of hyperpolarized Xe gas. It was found that the measured normalized Xe frequency shifts are significantly modified by the Xe polarization density, which causes different dipolar magnetic fields in the liquid and in the gas phases.

Journal Article↗

Investigation on the chemical structure of nonextractable residues of the fungicide cyprodinil in spring wheat using 13C-C1-phenyl-cyprodinil on 13C-depleted plants-an alternative approach to investigate nonextractable residues.

13C-labelled cyprodinil was applied on 13C-depleted wheat plants with 27-fold field application rate. A control experiment applying same amounts of 14C-cyprodinil showed that main portions of the residues were detected in the cellulose (15% NER), hemicellulose (28.3% NER), and lignin fraction (23.3% NER). 16.7% were detected in water soluble polymers, 6% in both, pectin and protein fraction, and 4% in the starch containing fraction. Free cyprodinil was detectable by TLC in all fractions except lignin. A direct characterization of the residues in vivo by CP-MAS was not successful. Cell wall fractions were further analysed by liquid state NMR to determine the structure of the mobilized highly polymer/polar residues: Within lignin, where most of the residues were located at field application rate, neither intact cyprodinil nor its metabolites could not be detected. The 13C-label introduced was probably incorporated in the polymer as natural lignin monomers and thus are not considered as bound residues according to IUPAC definition.

Carbon Isotopes↗

The pre-ribosomal network.

Recent achievements in yeast functional proteomics have significantly advanced our knowledge about ribosome biogenesis. Here, we present a program developed to integrate data from various proteome analyses with cell biological data on components present in the ribosome producing factories. This program allows users to attribute factors to certain complexes and to specific steps of ribosome biogenesis. Thus, it helps to gain novel insights into the complex network involved in maturation of ribosomal subunits. The database can be accessed at the URL http://www.pre-ribosome.de.

Biomarkers↗

A Noc complex specifically involved in the formation and nuclear export of ribosomal 40 S subunits.

Formation and nuclear export of 60 S pre-ribosomes requires many factors including the heterodimeric Noc1-Noc2 and Noc2-Noc3 complexes. Here, we report another Noc complex with a specific role in 40 S subunit biogenesis. This complex consists of Noc4p, which exhibits the conserved Noc domain and is homologous to Noc1p, and Nop14p, a nucleolar protein with a role in 40 S subunit formation. Moreover, noc4 thermosensitive mutants are defective in 40 S biogenesis, and rRNA processing is inhibited at early cleavage sites A(0), A(1), and A(2). Using a fluorescence-based visual assay for 40 S subunit export, we observe a strong nucleolar accumulation of the Rps2p-green fluorescent protein reporter in noc4 ts mutants, but 60 S subunit export was normal. Thus, Noc4p and Nop14p form a novel Noc complex with a specific role in nucleolar 40 S subunit formation and subsequent export to the cytoplasm.

Amino Acid Sequence↗

Molecular mobility in fixed-bed reactors investigated by multiscale NMR techniques.

The complex problem of a fixed-bed reactor consisting of catalytically active particles provides an exceptional opportunity of combining a wide range of NMR methods which have become available over time as tools to probe porous media. This work demonstrates the feasibility of different NMR techniques for the investigation of the intra- and interparticle pore space over length scales from nanometers up to centimeters. Many industrially relevant cracking reactions leave a coke residue on the inner surface of the porous catalyst particles so that the active sites become inaccessible to the reactants. Moreover, the pore space shrinks due to the formation of coke, thereby hindering molecular transport. The presence of the coke residue and its influence on the mobility of adsorbed fluid molecules are probed by 129Xe spectroscopy, NMR cryoporometry, relaxation dispersion measurements, and investigations of the reduced diffusivity in the intraporous space. The voids surrounding the random arrangement of catalyst pellets represent another pore space of much larger dimensions, the properties of which can be more directly investigated by mapping the fluid density and the velocity distribution from velocity-encoded imaging. Propagator representations averaged over large sample volumes are discussed and compared to velocity images obtained in selected axial slices of the reactor.

Alkanes↗