Theoretical aspects of 13C metabolic flux analysis with sole quantification of carbon dioxide labeling

The potential of using sole respirometric CO2 labeling measurement for 13C metabolic flux analysis was investigated by metabolic simulations. For this purpose a model was created, considering all CO2 forming and consuming reactions in the central catabolic and anabolic pathways. To facilitate the interpretation of the simulation results, the underlying metabolic network was parameterized by physiologically meaningful flux parameters such as flux partitioning ratios at metabolic branch points and reaction reversibilities. For real case flux scenarios of the industrial amino acid producer Corynebacterium glutamicum and different commercially available (13)C-labeled tracer substrates, observability and output sensitivity towards key flux parameters was investigated. Metabolic net fluxes in the central metabolism, involving, e.g. glycolysis, pentose phosphate pathway, tricarboxylic acid cycle, anaplerotic carboxylation, and glyoxylate pathway were found to be determinable by the respirometric approach using a combination of [1-13C] and [6-13C] glucose in two parallel studies. The reversibilities of bidirectional reactions influence the isotopic labeling of CO2 only to a negligible degree. On one hand, they therefore cannot be determined. On the other hand, their precise values are not required for the quantification of net fluxes. Computer-aided optimal experimental design was carried out to predict the quality of the information from the respirometric tracer experiments and identify suitable tracer substrates. A combination of [1-13C] and [6-13C] glucose in two parallel studies was found to yield a similar quality of information as compared to an approach with mass spectrometric labeling analysis of secreted products. The quality of information can be further increased by additional studies with [1,2-13C2] or [1,6-13C2] glucose. Respirometric tracer studies with sole labeling analysis of CO2 are therefore promising for 13C metabolic flux analysis.     

Electronic noise-free measurements of squeezed light

We study the implementation of a correlation measurement technique for the characterization of squeezed light. We show that the sign of the covariance coefficient revealed from the time-resolved correlation data allow us to distinguish among squeezed, coherent, and thermal states. In contrast to the traditional method of characterizing squeezed light, involving measurement of the variation of the difference photocurrent, the correlation measurement method allows one to eliminate the contribution of the electronic noise, which becomes a crucial issue in experiments with dim sources of squeezed light.     

Polymer and organic molecules ordered via epitaxy: geometrical and molecular interactions

Control of structural order at the molecular level for both conventional linear polymers and conjugated polymers with valuable opto‐electronic properties has major consequence on the macroscopic properties of these polymers. Though the traditional means of orientation of polymer was mechanical deformation, presently extensive works are concerned with a more controlled way of orientation: epitaxial crystallisation. Most of the first documented examples of epitaxial growth of conventional polymers on single crystals followed the well‐established geometrical rules of best matching. However, recent examples show off more subtle rules of selection. Analogous cases, following or breaking the matching rules, have been observed for diacetylenes ordered via epipolymerisation on single crystals. Hereafter, representative examples of the structural matching rules are depicted first, and then recent examples, which depart from the simple geometrical fitting, are described. The analysis of the former leads to define the subtle matching rules applying for polymers linked to their conformational adaptability. The analysis of the latter gives the opportunity to discuss the relative influence of geometrical and molecular interactions between the deposit and the substrate.     

Epitaxial crystallization of aliphatic polyesters on trioxane and various aromatic hydrocarbons

Linear polyesters of the diacid-dialcohol type are observed to crystallize epitaxially onto substrate crystals of trioxane, condensed aromatic hydrocarbons, and linear polyphenyls. In line with results previously reported for PE, lattice matching requirements for epitaxy lead to a change in the polymer contact plane on the different substrates. The highly oriented, sometimes single-crystal-like polymer films are formed of stacks of lamellae seen edge on which appear well suited to investigations of the lamellar structure.     

Kerr lens effects in a folded-cavity four-mirror linear resonator

The Kerr-lens model locking of a folded-cavity four-mirror linear Ti: sapphire laser is simulated by applying the ABCD ray-tracing technique for a Gaussian beam. The intensity dependent Kerr-lens ABCD matrix of the Brewster-plate shaped active medium is derived. A split-step parabolic refractive index model is used. the astigmatism compensation condition is derived from the ABCD ray-tracing. Simulations are carried out for a symmetric resonator and an asymmetric resonator design. Hard-aperture loss mode locking and soft-aperture gain mode locking are discussed. The optimum design parameters (slit position for hard-aperture loss mode locking, pump beam focusing for soft-aperture gain mode locking, gain cavity spacing, gain medium position) for Kerr-lens mode locking are determined.     

Polymer decoration study in chain folding behavior of solution-grown poly(ethylene oxide) crystals

The polymer decoration method based on the vaporization and condensation-crystallization of polyethylene (PE) upon the fold surface of polymer crystals has been widely used to study the chain folding behavior of the crystals. When this method was utilized to study solution-grown high molecular weight poly (ethylene oxide) (PEO) lamellar crystals, the highly anisotropic, low molecular weight fragment PE decorated become oriented parallel to the fold direction and form rods, which can be observed by transmission electron microscopy (TEM) and electron diffraction (ED). The growth sectors were clearly observed. From the ED patterns the {200} planes of the orthorhombic low molecular weight PE rod crystals can be observed, and the c-axis of these crystals is aligned parallel to the {120} growth planes of the PEO crystals. The decoration results indicate that the major fold orientation of high molecular weight PEO single crystals grown from dilute solution is along the {120} planes. © 1995 John Wiley & Sons, Inc.     

Umsetzungen einiger Malonester-enolbetaine mit Phenylisocyanat Über Reaktionen mit Betain, 7. Mitt.

Zusammenfassung Bis-alkoxycarbonylmethyl-pyridiniumenolbetaine, die als mesomere Enolbetaine vorliegen, reagieren mit Phenylisocyanat unter Abspaltung von Alkohol zu Pyrido-pyraziniumbetainen. Bis-phenoxymalonesterbetaine setzen sich dagegen, entsprechend ihrem Ylidcharakter, mit dem genannten Reagens unter Eliminierung von Diphenylcarbonat zu Derivaten des Pyridino-1.2.3.4-tetrahydro-pyrimidin-6-olates um.

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Reactions with betaine, VII: reactions of ethyl malonate-enolbetaines with phenyl isocyanate

Bis-alkoxycarbonylmethyl-pyridinium enolbetaines, which exist as mesomeric enolbetaines, react with phenyl isocyanate under the loss of ethanol to give pyrido-pyraziniumbetaines. However, phenyl malonate betaines react with phenyl isocyanate, according to their ylid character, to yield derivatives of 1.2.3.4-tetrahydro-pyrimidin-6-olates.

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Herrn Prof. Dr.M. Pailer, Wien, mit besten Wünschen zum 60. Geburtstag gewidmet.     

Elastic and inelastic diffraction of Mössbauer γ-rays from KCN

Mössbauer γ-ray diffraction was used to discriminate between the elastic and inelastic scattering intensities from the (1 1 1) to (5 5 5) Bragg reflections of a single crystal of KCN. The energy resolution of our experiment was 28 neV. We observe pronounced inelastic peaks at each Bragg point, while the elastic scattering dies out rapidly due to a large Debye-Waller factor. Thus in case of (4 4 4) and (5 5 5) the inelastic scattering is larger in magnitude than the elastic one.     

Nicht-tangentiales Randverhalten von harmonischen Funktionen in irregulären Randpunkten

Ohne Zusammenfassung