Pathways of hydrogen photoproduction by immobilized Chlamydomonas reinhardtii cells deprived of sulfur

The green algae Сhlamydomonas reinhardtii entrapped in a thin alginate film have been shown to sustain elevated rates of hydrogen photoproduction under anaerobic incubation in sulfur/phosphorus depleted tris-acetate medium. In the present work we studied mechanisms, underlying hydrogen photoproduction by the immobilized culture, particularly, the roles of PSII and starch accumulation/breakdown. DCMU, a specific inhibitor of electron transport in PSII, is known to suppress hydrogen evolution by circa 80% in suspension cultures of S-deprived C. reinhardtii. In immobilized cells DCMU caused successive stimulatory and inhibitory effects on hydrogen photoproduction, both depending on the deprivation status of the algal cell. The inhibitory effect of DCMU was 25% at 70 h of S deficiency when maximal rates of hydrogen photoproduction were observed. Measurements of the light-induced prompt and delayed chlorophyll fluorescence transients and reflectance at 820 nm (P₇₀₀ redox transitions) revealed very rapid decline of PSII activity in the entrapped S-deprived cells as compared with the suspension culture, whereas PSI suffered less. The immobilized culture showed a high capacity to accumulate starch during early stages of S deprivation and relatively high rates of anaerobic starch degradation during the following hydrogen evolution period. DCMU partly inhibited starch breakdown. Results of the present work brought us to the conclusion that PSII-independent pathway of hydrogen evolution is elevated in the immobilized S-deprived cells rather due to the rapid inactivation of PSII, efficient starch catabolism and non-photochemical PQ reduction.     

Monomolecular enzyme films stabilized by amphiphilic polyelectrolytes for biosensor devices

This paper describes the use of new amphiphilic polyelectrolytes for protein immobilization. Monomolecular films of glucose oxidase (GO) and monoamine oxidase (MAO) stabilized by amphiphilic polyelectrolytes (polyethyleneimine and poly-4-vinylpyridine derivatives modified by lauryl chains) were formed on a water surface in a Langmuir-Blodgett trough. The compressed films containing the enzymes were transferred onto the surface of a polypropylene membrane of a Clark electrode according to the Langmuir-Schaefer method. The analytical responses of the resulting biosensors were linear over the range 1–10 mM of glucose and 8–100 μM of tyramine. Furthermore, direct functional coupling of GO and ferrocenecarboxylic acid in multilayer films stabilized by amphiphilic polyelectrolytes was demonstrated. The amperometric response of such a sensor was linear over the range 1–20 mM of glucose. The dependence of the kinetic parameters of the enzymes on the amphiphilic polyelectrolyte structures is discussed.     

Precursor synthesis and properties of iron and lithium co-doped cadmium oxide

Journal of Electroceramics - Lithium and iron co-doped cadmium oxide Cd0.9(Li1-xFex)0.1O (x?=?0.1, 0.3, 0.5, 0.7) with NaCl structure has been synthesized using formate of the...     

Biological sensing and interface design in gold island film based localized plasmon transducers

Discontinuous, island-type gold films (typically < or = 10 nm nominal thickness) prepared by evaporation of the metal on transparent substrates show a localized surface plasmon resonance (LSPR) extinction in the visible-to-NIR range and can be used as optical transducers for monitoring local refractive index change. Such transducers, operated in the transmission configuration, provide an effective scheme for label-free biological sensing using basic spectrophotometric equipment. Optimization of the sensitivity of LPSR transducers requires consideration of the distance between the metal island surface and the bound analyte, strongly affecting the optical response due to the fast decay of the evanescent field of localized plasmons. In the present work Au island based LSPR transducers were used to monitor antibody-antigen interactions, demonstrating the effect of the biorecognition interface thickness. Evaporated Au island films derivatized with IgG or hCG antigens were used as biological recognition elements for selective sensing of antibody binding, distinguishing between specific and nonspecific interactions. The LSPR results are supported by XPS and ellipsometry data as well as by AFM and HRSEM imaging, the latter providing actual visualization of the two protein binding steps. Increase of the recognition interface thickness leads to a concomitant decrease in the extinction and wavelength sensitivity, generally conforming to a model of an exponentially decaying surface plasmon (SP) evanescent field.     

Shedding new light on the molecular architecture of oocytes using a combination of synchrotron Fourier transform-infrared and Raman spectroscopic mapping

Synchrotron Fourier transform-infrared (FT-IR) and Raman microspectroscopy were applied to investigate changes in the molecular architecture of mouse oocytes and demonstrate the overall morphology of the maturing oocyte. Here we show that differences were identified between immature mouse oocytes at the germinal vesicle (GV) and mature metaphase II (MII) stage when using this technology, without the introduction of any extrinsic markers, labels, or dyes. GV mouse oocytes were found to have a small, centrally located lipid deposit and another larger polar deposit of similar composition. MII oocytes have very large, centrally located lipid deposits. Each lipid deposit for both cell types contains an inner and outer lipid environment that differs in composition. To assess interoocyte variability, line scans were recorded across the diameter of the oocytes and compared from three independent trials (GV, n = 91; MII, n = 172), and the data were analyzed with principal component analysis (PCA). The average spectra and PCA loading plots show distinct and reproducible changes in the CH stretching region that can be used as molecular maturation markers. The method paves the way for developing an independent assay to assess oocyte status during maturation providing new insights into lipid distribution at the single cell level.     

Quadrefringence of optical vortices in a uniaxial crystal

The splitting of a single optical vortex into four separate ones in a singular beam is theoretically and experimentally described for the propagation of obliquely incident light in a uniaxial crystal. We also find the condition under which the generated vortices in each of the four individual beams propagate independently without changing their structure and have different locations in all beams for any crystal lengths.     

New and Uncommon Fatty Acids in Lipids of Deep-Sea Foraminifera

Fatty acids (FA) of agglutinating foraminifera of two genera, Bathysiphon and Rhabdammina, collected from a depth of 3307–3377 m in the Kuril Basin, Sea of Okhotsk, and adjacent deep‐sea waters of the Pacific Ocean, were analyzed. In lipids of two Bathysiphon species, in addition to common FA typical for marine organisms, the uncommon ?4 and ?7 monoenoic acids and ?4,7‐dienoic acid were found in noticeable amounts. FA of two Rhabdammina species included also such uncommon acids as ?5,8,11,14–21:4, ?5,8,11,14–22:4, and ?5,8,11,14–23:4, which are homologues to arachidonic acid. High levels of cis‐vaccenic and arachidonic acids were typical for lipids of all the studied species. At the same time, we observed a substantial difference in FA composition between members of these two genera. Using GC and GC–MS of FAME, pyrrolidide and DMOX derivatives, the structures of 10 new FA were confirmed: ?4‐i‐16:1 (1.1–0.6%), ?7‐i‐21:1 (0.4%), ?7‐ai‐21:1 (0.3–0.8%), ?4,11–18:2 (0.3–0.9%), ?4,7–20:2 (8.8%), ?7,12–20:2 (0.4–0.6%), ?4,7–21:2 (0.6%), ?7,12–22:2 (6.4–2.1%); ?5,8,11,14–22:4 (1.2–2.0%), and ?5,8,11,14–23:4 (1.7–2.3%). The origin of the new FA and the role of foraminifera FA in deep‐sea communities are discussed.     

Structure and mechanical properties of the compositions of polyisocyanurate polymers with low molecular weight rubbers

The structure and properties of the compositions of polyisocyanurates modified with low molecular weight rubber networks have been investigated by means of dynamical mechanical analysis (DMA), electron microscopy, and stress-relaxation experiments. The network compositions consist of two different polymeric networks. The first component (macrodi-isocyanate based on low molecular weight polybutadiene or copolymers of tetrahydrofuran and propylene oxide) has bulky cross-linked points connected by short flexible chains. The second component (diphenylmethanediisocyanate) also has bulky cross-linked points of the same structure, but the linear fragments between them in this case are very small and rigid. These compositions result in the formation of the heterophase system. As a result, transparent samples were prepared, which differ from the mechanical properties of both the glassy and rubbery polymers. These materials have a modulus of elasticity (from 10³ to 10 MPa) that is usual for the transition zone between the glassy and rubbery states; nevertheless, these materials show elastic (and not viscoelastic) properties. For the materials investigated, the modulus is decreased not more than 10 times in the wide temperature interval from 200 to 500 K. A new state of the polymer, which differs from both the glassy and rubbery states, has been identified in the present case. © 1995 John Wiley & Sons, Inc.