Determining the binding affinities of phenolic compounds to proteins by quenching of the intrinsic tryptophan fluorescence

The noncovalent binding of selected phenolic compounds (chlorogenic-, ferulic-, gallic acid, quercetin, rutin, and isoquercetin) to proteins (HSA, BSA, soy glycinin, and lysozyme) was studied by an indirect method applying the quenching of intrinsic tryptophan fluorescence. From the data obtained, the binding constants were calculated by nonlinear regression (one site binding; y = Bx/k + x). It has been reported that tannins inhibit human salivary amylase and that these complexes may reduce the development of cariogenic plaques. Further, amylase contains two tryptophan residues in its active site. Therefore, in a second part of the study involving 31 human subjects, evidence was sought for noncovalent interactions between the phenols of green tea and saliva proteins as measured by the fluorescence intensity. Amylase activity was determined before and after the addition of green tea to saliva of 31 subjects. Forty percent of the subjects showed an increase in amylase activity contrary to studies reporting only a decrease in activity. The interactions of tannin with amylase result in a decrease of its activity. It still remains to be elucidated why amylase does not react uniformly under conditions of applying green tea to saliva. Further, in terms of using phenols as caries inhibitors this finding should be of importance.     

Numerical parametric lens for shifting, magnification, and complete aberration compensation in digital holographic microscopy

The concept of numerical parametric lenses (NPL) is introduced to achieve wavefront reconstruction in digital holography. It is shown that operations usually performed by optical components and described in ray geometrical optics, such as image shifting, magnification, and especially complete aberration compensation (phase aberrations and image distortion), can be mimicked by numerical computation of a NPL. Furthermore, we demonstrate that automatic one-dimensional or two-dimensional fitting procedures allow adjustment of the NPL parameters as expressed in terms of standard or Zernike polynomial coefficients. These coefficients can provide a quantitative evaluation of the aberrations generated by the specimen. Demonstration is given of the reconstruction of the topology of a microlens.     

Submicrometer optical tomography by multiple-wavelength digital holographic microscopy

We present a method for submicrometer tomographic imaging using multiple wavelengths in digital holographic microscopy. This method is based on the recording, at different wavelengths equally separated in the k domain, in off-axis geometry, of the interference between a reference wave and an object wave reflected by a microscopic specimen and magnified by a microscope objective. A CCD camera records the holograms consecutively, which are then numerically reconstructed following the convolution formulation to obtain each corresponding complex object wavefront. Their relative phases are adjusted to be equal in a given plane of interest and the resulting complex wavefronts are summed. The result of this operation is a constructive addition of complex waves in the selected plane and destructive addition in the others. Tomography is thus obtained by the attenuation of the amplitude out of the plane of interest. Numerical variation of the plane of interest enables one to scan the object in depth. For the presented simulations and experiments, 20 wavelengths are used in the 480-700 nm range. The result is a sectioning of the object in slices 725 nm thick.     

Phase Evolution in and Creep Properties of Nb-Rich Nb-Si-Cr Eutectics

In this work, the Nb-rich ternary eutectic in the Nb-Si-Cr system has been experimentally determined to be Nb-10.9Si-28.4Cr (in at. pct). The eutectic is composed of three main phases: Nb solid solution (Nb_ss), β-Cr₂Nb, and Nb₉(Si,Cr)₅. The ternary eutectic microstructure remains stable for several hundred hours at a temperature up to 1473 K (1200 °C). At 1573 K (1300 °C) and above, the silicide phase Nb₉(Si,Cr)₅ decomposes into α-Nb₅Si₃, Nb_ss, and β-Cr₂Nb. Under creep conditions at 1473 K (1200 °C), the alloy deforms by dislocation creep while the major creep resistance is provided by the silicide matrix. If the silicide phase is fragmented and, thus, its matrix character is destroyed by prior heat treatment [e.g., at 1773 K (1500 °C) for 100 hours], creep is mainly controlled by the Laves phase β-Cr₂Nb, resulting in increased minimum strain rates. Compared to state of the art Ni-based superalloys, the creep resistance of this three-phase eutectic alloy is significantly higher.     

Carbon‐Carbon Double Bond versus Carbonyl Group Hydrogenation: Controlling the Intramolecular Selectivity with Polyaniline‐Supported Platinum Catalysts

The use of polyaniline (PANI) as catalyst support for heterogeneous catalysts and their application in chemical catalysis is hitherto rather poorly known. We report the successful synthesis of highly dispersed PANI‐supported platinum catalysts (particle sizes between 1.7 and 3.7 nm as revealed by transmission electron microscopy, TEM) choosing two different approaches, namely (i) deposition‐precipitation of H₂PtCl₆ onto polyaniline, suspended in basic medium (DP method) and, (ii) immobilization of a preformed nanoscale platinum colloid on polyaniline (sol‐method). The PANI‐supported platinum catalysts were applied in the selective hydrogenation of the α,β‐unsaturated aldehyde citral. In order to benchmark their catalytic performance, citral hydrogenation was also carried out by using platinum supported on the classical support materials silica (SiO₂), alumina (Al₂O₃), active carbon and graphite. The relations of the structural characteristics and surface state of the catalysts with respect to their hydrogenation properties have been probed by EXAFS and XPS. It is found that the DP method yields chemically prepared PtO₂ on polyaniline and, thus, produces a highly dispersed and immobilized Adams catalyst (in the β‐PtO₂ form) which is able to efficiently hydrogenate the conjugated CC bond of citral (selectivity to citronellal=87%), whereas reduction of the CO group occurs with polyaniline‐supported platinum (selectivity to geraniol/nerol=78%) prepared via the sol‐method. The complete reversal of the selectivity between the preferred hydrogenation of the conjugated CC or CO group is not only particularly useful for the selective hydrogenation of α,β‐unsaturated aldehydes but also unveils the great potential of conducting polymer‐supported precious metals in the field of hitherto barely investigated chemical catalysis.     

TUM–WelChem cell model for the prediction of liquid distribution in random packed columns

Liquid maldistribution is one of the main deficiencies in random packed column design. Therefore, the knowledge of liquid distribution and its model-based prediction is of great interest. This work aims to further develop and validate the TUM–WelChem Cell Model for random packed columns. First, cell dimension calculations and the determination of random packing element orientations are standardized. The original WelChem Cell Model applies a liquid distribution mechanism based on liquid spread factors derived by virtual 3D irrigation experiments. An extension of the model involves the implementation of liquid and gas load related distribution mechanisms, considering dispersion effects caused by liquid loading and the countercurrent gas flow. The wall flow is refined by an increase of packing porosity at the column wall. Liquid distribution profiles provided by the TUM–WelChem Cell Model are validated against experimental data and show good agreement for both uniform and point source initial liquid distribution.