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[Electronic structures of organometallic complexes of f elements. Part 54. Electronic Raman and f-f transitions in the low temperature vibrational spectra of Cp3Ce(NCCH3)2].

A comparison of the low temperature Raman spectra of Cp(3)Ce(NCCH(3))(2) (1), Cp(3)La(NCCH(3))(2) (2), Cp(3)La(NCCH(3))(2):Pr(3+) (3), Cp(3)La x NCCH(3) (4), Cp(3)Ce x NCCH(3) (5) and Cp(3)Tb x NCCH(3) (6) shows that the former compound exhibits three additional bands at 320, 2129 and 2154 cm(-1), which we ascribe to electronic Raman transitions. The two latter signals also appear in the low temperature IR spectrum of complex 1, but not in those of compounds 2-6. By performing crystal field (CF) calculations, the terminal states of the observed electronic Raman transitions could be identified. On the basis of both experimental and calculated CF energies as well as calculated wave functions the observed temperature dependence of mu(2)(eff) of complex 1 could be simulated in a satisfactory manner. A comparison of the low temperature Raman spectrum of compound 1 with the low temperature FIR spectrum of complex 2 shows that the selection rules for trigonal-bipyramidal coordination do not hold strictly for the skeletal vibrations. If the additional criterion of allowed vibronic side bands is applied to the transitions Gamma(1)-->Gamma(1, 4, 5, 6) of compound 3, the observed vibrational energies may be partly classified according to their symmetry.

Cerium↗

Structural changes in the Schiff base region of squid rhodopsin upon photoisomerization studied by low-temperature FTIR spectroscopy.

Low-temperature Fourier transform infrared (FTIR) spectroscopy is used to study squid rhodopsin at 77 K in investigating structural changes in the Schiff base region upon photoisomerization. The analysis of O-D stretching vibrations in D(2)O revealed that there are more internal water molecules near the retinal chromophore in squid rhodopsin than in bovine rhodopsin. Among nine O-D stretching vibrations of water in squid rhodopsin, eight peaks are identical between rhodopsin and 9-cis-rhodopsin (Iso). On the other hand, the isomer-specific O-D stretch of water was observed for rhodopsin (2451 cm(-)(1)) and Iso (2382 cm(-)(1)). Low frequencies of these bands suggest that the water forms a strong hydrogen bond with a negatively charged counterion. In addition, it was suggested that the hydrogen bond of the Schiff base is weaker in squid rhodopsin than in bacteriorhodopsin and bovine rhodopsin, and squid rhodopsin possessed similar hydrogen bonding strength for the Schiff base among rhodopsin, Iso, and bathorhodopsin. Most vibrational bands in the X-D stretch region originate from water O-D or the Schiff base N-D stretches, suggesting that the hydrogen bonding network in the Schiff base region of squid rhodopsin is composed of only water molecules. On the basis of these results, we propose that squid rhodopsin possesses a "bridge" water between the Schiff base and its counterion as well as squid retinochrome [Furutani, Y., Terakita, A., Shichida, Y., and Kandori, H. (2005) Biochemistry 44, 7988-7997], which is absent in vertebrate rhodopsin [Furutani, Y., Shichida, Y., and Kandori, H. (2003) Biochemistry 42, 9619-9625].

Animals↗

Effects of molybdenum on antioxidative defense system and membrane lipid peroxidation in winter wheat under low temperature stress.

Effects of molybdenum (Mo) on antioxidative defense system and membrane lipid peroxidation in leaves of winter wheat (Triticum aestivum H. var. Huamai 8) were investigated under low temperature stress. Results of experiments indicate that Mo application in winter wheat induced a dramatic decrease in electrolyte leakage and malondialdehyde content under low temperature stress. The activities of antioxidative enzymes such as superoxide dismutase (SOD, EC 1.15.1.1), peroxidase (POX, EC 1.11.1.7) and catalase (CAT, EC 1.11.1.6) were increased by Mo application and the extents of increase at low temperature were higher than those at normal temperature. Mo application also caused a significant increase in the ascorbic acid (AsA) and proline contents both at normal and low temperature and following the low temperature stress the increases in ascorbic acid and proline contents in Mo-treated winter wheat were higher. There was no significant difference in carotenoid (CAR) content between with and without Mo treatment under normal temperature, while there was a significant increase in Mo treatment under low temperature stress. It could be speculated that Mo application enhanced cold resistance by increasing the capacity to scavenge active oxygen species and alleviating membrane damage in winter wheat under low temperature stress.

Ascorbic Acid↗

[Changes in the cuticle of a keratin fiber under the action of a low-temperature plasma].

Oxygen and air low-temperature plasma treatment leads to significant changes in fibre cuticle cell membrane (skin flakes). Both lipids and proteins were destroyed. The processes of intensive lipid oxidation resulted from low-temperature plasma action. This factor seems to change critical surface tension, wetting and increasing penetration of dyes through the cuticle.

Air↗

Adreno- and cholinoreactivity of the vascular system under the influence of low temperature.

The influence of low temperature results in the activation of a sympathetic division of the vegetative nervous system (mostly alpha2-artery adrenoreceptors). The data concerning the tone of the parasympathetic department are inconsistent. In studies carried out in experimental animals (rabbits), the cholinoreactivity of arterial vessels was investigated. After a single cooling the depressing action of acetylcholin on arterial vessels grows only because of an increase of the quantity of active (Pm) M-cholinoreceptors of vessels (by 66.6%) with a decrease of their sensitivity (1/K = 4) by 33.3%. By day 30 of cold depressing adaptation the action of acetylcholin grows (with doses 0.02-0.1 mkg/kg) only because of an increase of M-cholinoreceptors sensitivity by 233%. The reduction of the depressing action on arteries of acetylcholin with dozes of 0.2-0.8 mkg/kg is explained by a decrease of the quantity of active M-cholinoreceptors in these terms of the cold influence (by 41% as compared with a control group). According to the results the efficiency of the interaction (E = (Pm/2)*R)) of acetylcholin with M-cholinoreceptors of vessels grows by 96% (with E = 300 mm/m.c./1 mkg/kg in a control group up to E = 588 after 30 day's adaptation to cold).

Adaptation, Physiological↗

[Photoinduced electron transfer through the hydrocarbon zone of membranes at low temperatures].

The photoinduced electron transfer at low temperatures in phospholipide membranes (liposomes) containing chlorophyll and 3 X 10-docsilpalmitate has been investigated. The reduction of 3 X 10-docsilpalmitate was estimated by ESR spectrometry. When diffusion movement of the molecules in membranes was blocked by low temperatures the photoinduced electron transfer has been found. The mechanism of these phenomena were analyzed on the base of donor-acceptor interaction through sigma bonds in hydrocarbon bridged donor-acceptor complexes. The separation of charges in these complexes is regarded as occurs by the migration of a hole along the hydrocarbon system. An approximate estimate of the charge mobility in the saturated hydrocarbon side chain of chlorophyll and activation energy of these movement was obtained.

Chlorophyll↗

[Various approaches to studying molecular-genetic mechanisms of low-temperature adaptation of microbial populations].

The effect of biologically low temperature (12 degrees C) on the parameters of microbial population such as survival, catalase activity and its isoenzyme spectrum have been investigated on the models of Escherichia coli and Yersinia pseudotuberculosis. The quantity of nucleic acids, plasmid spectrum and temperature effect on the level of plasmid DNA spiralization were studied under these conditions. The process of molecular genetic adaptation of bacterial populations having the broad temperature limits of growth and demonstrating the increased genetical expression when affected by the biologically low temperature has been found to be regulated on the transcriptional level. The inducible catalase isoenzymes participate in adaptation. The effect of biologically low temperature on the level of the plasmid DNA superhelicity and DNA quantity during the short period of poststress was not demonstrated.

Adaptation, Physiological↗

On-block UV light polymerization of LR Gold-embedded flat-mounted tissue using low temperature modules.

A problem associated with low temperature embedding is due to the fact that suitable resins have to be polymerized under oxygen-free atmosphere, thus making the complete filling and tight sealing of vials or capsules essential. Particularly with thin tissue sections or retinal flat-mounts it is rather difficult to obtain flat-embedded specimens under these conditions. To overcome this problem, we have designed a low temperature module (LTM) that allows the polymerization of flat tissue probes on faced resin blocks using UV light, thus instantly creating ready specimens with an almost planar surface. To test the device, vibratome sections of the rat superior colliculus were embedded in LR Gold and UV-cured in LTMs. Electron microscopy revealed a good preservation of the fine structure. The new UV light polymerization technique proved to be highly suitable to obtain ultrathin sections being cut parallel to the surface of the embedded material, an advantageous feature for applications which necessitate the examination of specifically oriented or laminated structures. Detailed and dimensioned drawings of the LTM can be downloaded as a PDF file at: http://www.uni-leipzig.de/-vetana.

Animals↗

Low-temperature studies of encapsulated proteins.

Water-soluble proteins encapsulated within reverse micelles may be studied under a variety of conditions, including low temperature and a wide range of buffer conditions. Direct high-resolution detection of information relating to protein folding intermediates and pathways can be monitored by low-temperature solution NMR. Ubiquitin encapsulated within AOT reverse micelles was studied using multidimensional multinuclear solution NMR to determine the relationship between protein structure, temperature, and ionic strength. Ubiquitin resonances were monitored by 15N HSQC NMR experiments at varying temperatures and salt concentrations. Our results indicate that the structure of the encapsulated protein at low temperature experiences perturbation arising from two major influences, which are reverse micelle-protein interactions and low-temperature effects (e.g., cold denaturation). These two effects are impossible to distinguish under conditions of low ionic strength. Elevated concentrations of nondenaturing salt solutions defeat the effects of reverse micelle-protein interactions and reveal low-temperature protein unfolding. High ionic strength shielding stabilizes the reverse micelle at low temperatures, which reduces the electrostatic interaction between the protein and reverse micelle surfaces, allowing the phenomenon of cold denaturation to be explored.

Cold Temperature↗

The BtpA protein stabilizes the reaction center proteins of photosystem I in the cyanobacterium Synechocystis sp. PCC 6803 at low temperature.

Specific inhibition of photosystem I (PSI) was observed under low-temperature conditions in the cyanobacterium Synechocystis sp. strain PCC 6803. Growth at 20 degrees C caused inhibition of PSI activity and increased degradation of the PSI reaction center proteins PsaA and PsaB, while no significant changes were found in the level and activity of photosystem II (PSII). BtpA, a recently identified extrinsic thylakoid membrane protein, was found to be a necessary regulatory factor for stabilization of the PsaA and PsaB proteins under such low-temperature conditions. At normal growth temperature (30 degrees C), the BtpA protein was present in the cell, and its genetic deletion caused an increase in the degradation of the PSI reaction center proteins. However, growth of Synechocystis cells at 20 degrees C or shifting of cultures grown at 30 degrees C to 20 degrees C led to a rapid accumulation of the BtpA protein, presumably to stabilize the PSI complex, by lowering the rates of degradation of the PsaA and PsaB proteins. A btpA deletion mutant strain could not grow photoautotrophically at low temperature, and exhibited rapid degradation of the PSI complex after transfer of the cells from normal to low temperature.

Bacterial Proteins↗

Integration of transcriptomic and metabolic analyses for understanding the global responses of low-temperature winemaking fermentations.

Wine produced at low temperature is often considered to have improved sensory qualities. To investigate the effects of temperature on winemaking, the expression patterns during the industrial fermentation process carried out at 13 degrees C and 25 degrees C were compared, and correlated with physiological and biochemical data, including viability, fermentation byproducts and lipid content of the cells. From a total of 535 ORFs that were significantly differentially expressed between the 13 degrees C and 25 degrees C fermentations, two significant transcription programmes were identified. A cold-stress response was expressed at the initial stage of the fermentation, and this was followed by a transcription pattern of upregulated genes concerned with the cell cycle, growth control and maintenance in the middle and late stages of the process at 13 degrees C with respect to 25 degrees C. These expression patterns were correlated with higher cell viability at low temperature. The other relevant transcriptomic difference was that several genes implicated in cytosolic fatty acid synthesis were downregulated, while those involved in mitochondrial short-chain fatty acid synthesis were upregulated in the fermentation process conducted at 13 degrees C with respect to that at 25 degrees C. These transcriptional changes were qualitatively correlated with improved resistance to ethanol and increased production of short-chain (C(4)-C(8)) fatty acids and their corresponding esters at 13 degrees C as compared to 25 degrees C. While this increase of ethyl esters may account in part for the improved sensory quality of wine fermented at 13 degrees C, it is still unclear how the esterification of the short-chain fatty acids takes place. On the basis of its strong upregulation at 13 degrees C, we propose a possible role of IAH1 encoding an esterase/ester synthase in this process.

Cold Temperature↗

Metallurgy in a beaker: nanoparticle toolkit for the rapid low-temperature solution synthesis of functional multimetallic solid-state materials.

Intermetallic compounds and alloys are traditionally synthesized by heating mixtures of metal powders to high temperatures for long periods of time. A low-temperature solution-based alternative has been developed, and this strategy exploits the enhanced reactivity of nanoparticles and the nanometer diffusion distances afforded by binary nanocomposite precursors. Prereduced metal nanoparticles are combined in known ratios, and they form nanomodulated composites that rapidly transform into intermetallics and alloys upon heating at low temperatures. The approach is general in terms of accessible compositions, structures, and morphologies. Multiple compounds in the same binary system can be readily accessed; e.g., AuCu, AuCu3, Au3Cu, and the AuCu-II superlattice are all accessible in the Au-Cu system. This concept can be extended to other binary systems, including the intermetallics FePt3, CoPt, CuPt, and Cu3Pt and the alloys Ag-Pt, Au-Pd, and Ni-Pt. The ternary intermetallic Ag2Pd3S can also be rapidly synthesized at low temperatures from a nanocomposite precursor comprised of Ag2S and Pd nanoparticles. Using this low-temperature solution-based approach, a variety of morphologically diverse nanomaterials are accessible: surface-confined thin films (planar and nonplanar supports), free-standing monoliths, nanomesh materials, inverse opals, and dense gram-scale nanocrystalline powders of intermetallic AuCu. Importantly, the multimetallic materials synthesized using this approach are functional, yielding a room-temperature Fe-Pt ferromagnet, a superconducting sample of Ag2Pd3S (Tc = 1.10 K), and a AuPd4 alloy that selectively catalyzes the formation of H2O2 from H2 and O2. Such flexibility in the synthesis and processing of functional intermetallic and alloy materials is unprecedented.

Journal Article↗

Use of low temperatures for glutathione histochemical stain.

We performed glutathione (GSH) staining at a low temperature to prevent GSH release from the section and, hence, improve morphology. Fresh frozen sections of liver, lung, kidney, heart, and stomach were incubated for GSH activity in an ice bath (2-5 degrees C) for 5-10 min. Low temperature incubation prevented GSH diffusion out of cells and minimized migration of granules into vessels and outside of tissue. Incubation at low temperature generally reduced the intensity of the stain compared to the standard method. We conclude that low temperature incubation improves GSH localization in cells, probably by regulating the rate, formation, and the size of GSH-mercury orange complexes.

Animals↗

Monounsaturated but not polyunsaturated fatty acids are required for growth of the deep-sea bacterium Photobacterium profundum SS9 at high pressure and low temperature.

There is considerable evidence correlating the production of increased proportions of membrane unsaturated fatty acids (UFAs) with bacterial growth at low temperatures or high pressures. In order to assess the importance of UFAs to microbial growth under these conditions, the effects of conditions altering UFA levels in the psychrotolerant piezophilic deep-sea bacterium Photobacterium profundum SS9 were investigated. The fatty acids produced by P. profundum SS9 grown at various temperatures and pressures were characterized, and differences in fatty acid composition as a function of phase growth, and between inner and outer membranes, were noted. P. profundum SS9 was found to exhibit enhanced proportions of both monounsaturated (MUFAs) and polyunsaturated (PUFAs) fatty acids when grown at a decreased temperature or elevated pressure. Treatment of cells with cerulenin inhibited MUFA but not PUFA synthesis and led to a decreased growth rate and yield at low temperature and high pressure. In addition, oleic acid-auxotrophic mutants were isolated. One of these mutants, strain EA3, was deficient in the production of MUFAs and was both low-temperature sensitive and high-pressure sensitive in the absence of exogenous 18:1 fatty acid. Another mutant, strain EA2, produced little MUFA but elevated levels of the PUFA species eicosapentaenoic acid (EPA; 20:5n-3). This mutant grew slowly but was not low-temperature sensitive or high-pressure sensitive. Finally, reverse genetics was employed to construct a mutant unable to produce EPA. This mutant, strain EA10, was also not low-temperature sensitive or high-pressure sensitive. The significance of these results to the understanding of the role of UFAs in growth under low-temperature or high-pressure conditions is discussed.

Cell Membrane↗

Studies on the adaptation of influenza virus replicated at low temperature. III. Biochemical studies.

Five strains of influenza viruses A(H3N2) replicated at low temperature passaged in cotton rats were reisolated. The properties of these strains replicated at low temperature were compared before and after passage in susceptible animals to check the stability of some its markers. At the same time original viruses replicated at 37 degrees C--which are different in epidemiological potency--were compared. The following parameters being tested: NA activity, HA titers, heat inactivation NA and Ha, Michaelis constants and optimum pH. We observed some differences between strains both replicated at low temperature after passage in the susceptible animal organism and original viruses from 37 degrees C. Viruses replicated at low temperature from original epidemiostrain are really cold adapted and remained stable after passage in the animals when the others derived from no epidemic strain are not stable.

Adaptation, Physiological↗

Induction of the acrosome reaction in sperm by exposure to low temperature increases their rate of fusion with zona-free hamster oocytes.

The fusion rate of human sperm with zona-free hamster ova was investigated after induction of the acrosome reaction by exposure to a low temperature (4 degrees C). Sperm were collected from 14 patients, and selected by the 'swim-up' method. The sperm were incubated for 24 h at either room temperature (control group) or at 4 degrees C (low temperature group), followed by additional incubation at 37 degrees C for 3 h. The mean sperm penetration rate, number of swollen sperm heads as well as the number of sperm attached to the oocyte increased significantly after exposing sperm to low temperature. The sperm penetration rate showed a significant correlation (Spearman test, r = 0.572, n = 28, P less than 0.0035) with the acrosome reaction in the low temperature group. These results were associated with an increase in the rate of penetration of hamster ova observed in this study, presumably due to the increase in induction of the acrosome reaction by low temperature. Incubation of sperm at low temperature might be useful in the evaluation of so-called false negative results in the zona-free hamster test.

Acrosome↗

Comprehensive expression analysis of time-dependent genetic responses in yeast cells to low temperature.

We performed genome-wide expression analysis to determine genetic responses in Saccharomyces cerevisiae to a low temperature environment using a cDNA microarray. Approximately 25% of the genes in the yeast genome were found to be involved in the response of yeast to low temperature. This finding of a large number of genes being involved in the response to low temperature enabled us to give a functional interpretation to the genetic responses to the stimulus. Functional and clustering analyses of temporal changes in gene expression revealed that global states of the expressions of up-regulated genes could be characterized as having three phases (the early, middle, and late phases). In each phase, genes related to rRNA synthesis, ribosomal proteins, or several stress responses are time-dependently up-regulated, respectively. Through these phases, yeast cells may improve reduced efficiency of translation and enhance cell protection mechanisms to survive under a low temperature condition. Furthermore, these time-dependent regulations of these genes would be controlled by the cAMP-protein kinase A pathway. The results of our study provide a global description of transcriptional response for adaptation to low temperature in yeast cells.

Cyclic AMP↗

Mechanism of enhanced positronium formation in low-temperature polymers.

An enhanced positronium (Ps) formation in low-temperature polymers has been widely observed. The additional positronium formation is due to shallow trapped electrons in them. Positron annihilation lifetime spectroscopy was applied to investigate the Ps formation in a series of polymers, such as low-density polyethylene, ethylene-methyl methacrylate copolymers with various methyl methacrylate contents, and pure poly(methyl methacrylate) at low temperature. An analysis of the experimental data based on simple kinetic equations enables one to understand the Ps formation mechanism in polymers during low-temperature positron annihilation experiments as functions of the temperature and elapsed time. Good fittings of the experimental data were obtained. The fitting parameters seemed to show clear physical meanings.

Journal Article↗