Effect of treatment with electrolyzed NaCl solutions and essential oil compounds on the proximate composition,amino acid and fatty acid composition of carp fillets

This investigation was undertaken to evaluate the effect of treatment with electrolyzed NaCl solutions and 1% essential oil (0.5% carvacrol + 0.5% thymol) on the proximate composition and nutritional components (amino acids and fatty acids) of carp fillets at room temperature (25 °C). Carp fillet samples were treated with anodic electrolyzed NaCl solution [EW (+)], cathodic electrolyzed NaCl solution [EW (−)] followed by EW (+) [EW (−)/EW (+)], 1% essential oil (0.5% carvacrol + 0.5% thymol) [1% (Cv + Ty)], EW (+) followed by 1% (Cv + Ty) [EW (+)/1% (Cv + Ty)] and EW (−) followed by EW (+) and finally with 1% (Cv + Ty) [EW (−)/EW (+)/1% (Cv + Ty)]. Proximate composition, SDS–PAGE, amino acid composition, digestibility and fatty acid composition were used to determine the changes in carp fillet composition. Moisture, total lipid, total protein, ash and carbohydrate contents of the carp fillets were approximately 76%, 3.9%, 17.5%, 1.0% and 0.40%, respectively. The dominant amino acid was glutamic acid, and the composition ranged from 14.2 to 14.5 mol%. Protein digestibility of the carp fillets was approximately 85%. Oleic acid was the major monounsaturated acid in the carp fillets (41.0–41.9%). These results show that our method of fish preservation, using electrolyzed NaCl solutions and 1% (Cv + Ty), did not affect the quality (nutritional components) of carp fillets, and could be a good alternative to synthetic preservatives routinely used in the food industry.     

Overexpression of the Bcl-2 protein increases the half-life of p21Bax

Bcl-2 and Bax are homologous proteins which can heterodimerize with each other. These proteins have opposing effects on cell survival when overexpressed in cells, with Bcl-2 blocking and Bax promoting apoptosis. Here we demonstrate that gene transfer-mediated elevations in Bcl-2 protein levels result in a marked increase in the steady-state levels of endogenous p21Bax protein as determined by immunoblotting in the Jurkat T-cell and 697 pre-B-cell leukemia cell lines, but not in several other cell lines including CEM T-cell leukemia, 32D.3 myeloid progenitor, PC12 pheochromocytoma, and NIH-3T3 fibroblasts. Steady-state levels of p21Bax protein were also elevated in the lymph nodes of Bcl-2 transgenic mice in which a BCL-2 transgene is expressed at high levels in B-cells. Northern blot analysis of BCL-2-transfected and control-transfected Jurkat and 697 leukemia cells revealed no Bcl-2-induced alterations in the steady-state levels of BAX mRNAs. In contrast, L-[35S]methionine pulse-chase analysis indicated a marked increase in the half-life (t1/2) of the p21Bax protein in BCL-2-transfected 697 cells compared to control-transfected cells (t1/2 > 24 h versus approximately 4 h), whereas the rate of Bax degradation was unaltered in Bcl-2-transfected CEM cells. The results demonstrate that levels of the proapoptotic p21Bax protein can be post-translationally regulated by Bcl-2, probably in a tissue-specific fashion, and suggest the existence of a feedback mechanism that may help to maintain the ratio of Bcl-2 to Bax protein in physiologically appropriate ranges.     

Spreading behavior of polymerizable monolayers of acrylamides with double alkyl chains and polymerization of the LB films

The spreading behavior of N,N'-dialkylacrylamide (dAAs) monomers on a water surface is investigated by measurement of surface pressure-area isotherms as a function of alkyl chain length and temperature. The monolayers of dAAs can be classified into three types. (I) N,N'-dioctadecylacrylamide (dODA) shows a rapid increase in surface pressure indicating formation of a rigid condensed monolayer; (II) the isotherm of N,N'-dihexadecylacrylamide (dHDA) has a plateau region in surface pressure corresponding to a phase transition from a expanded form to a condensed form, which corresponds to gel-liquid crystal phase transition often observed in biomembranes; and (III) the dialkylacrylamides with alkyl chain length shorter than the hexadecyl group form expanded monolayers with no condensed monolayer at any temperature. The similar three kinds of monolayers are also observed in the isotherms for dHDA monolayer as a function of temperature. It is found that two carbon elongation in double alkyl chains causes the same effect on the monolayer induced by about 10 °C cooling. Under various conditions, only liquid condensed monolayers are transferred on to a solid support, yielding the monomer LB films, practically, of dODA at any temperature and dHDA at low temperature. The polymerization of those LB films by UV irradiation was ascertained by the electronic absorption spectra.     

Plasmon analyses of Triticum (wheat) and Aegilops: PCR-single-strand conformational polymorphism (PCR-SSCP) analyses of organellar DNAs

To investigate phylogenetic relationships among plasmons in Triticum and Aegilops, PCR-single-strand conformational polymorphism (PCR-SSCP) analyses were made of 14.0-kb chloroplast (ct) and 13. 7-kb mitochondrial (mt)DNA regions that were isolated from 46 alloplasmic wheat lines and one euplasmic line. These plasmons represent 31 species of the two genera. The ct and mtDNA regions included 10 and 9 structural genes, respectively. A total of 177 bands were detected, of which 40.6% were variable. The proportion of variable bands in ctDNA (51.1%) was higher than that of mtDNA (28. 9%). The phylogenetic trees of plasmons, derived by two different models, indicate a common picture of plasmon divergence in the two genera and suggest three major groups of plasmons (Einkorn, Triticum, and Aegilops). Because of uniparental plasmon transmission, the maternal parents of all but one polyploid species were identified. Only one Aegilops species, Ae. speltoides, was included in the Triticum group, suggesting that this species is the plasmon and B and G genome donor of all polyploid wheats. ctDNA variations were more intimately correlated with vegetative characters, whereas mtDNA variations were more closely correlated with reproductive characters. Plasmon divergence among the diploids of the two genera largely paralleled genome divergence. The relative times of origin of the polyploid species were inferred from genetic distances from their putative maternal parents.     

A new technology for fish preservation by combined treatment with electrolyzed NaCl solutions and essential oil compounds

This study was undertaken to establish a new technology, using pre-treatment with electrolyzed NaCl solutions and essential oil compounds, to extend the shelf-life of carp fillets. Samples of skinless carp fillets were treated with 100-fold (by weight) of electrolyzed NaCl solutions [cathodic solution, EW(−) and/or anodic solution, EW(+)] and 1% oil (0.5% carvacrol + 0.5% thymol) [1%(C + T)]. Then chemical [pH, volatile basic nitrogen, peroxide value, and thiobarbituric acid], microbiological (total viable count) and sensory analyses were used to evaluate the preservative effect of this new technology during storage at 5 and 25 °C. Our results from the chemical assays indicated that EW(−), followed by EW(+) and subsequently 1%(C + T) [EW(−)/EW(+)/1%(C + T)], significantly suppressed the lipid oxidation compared with other treatments. Data from sensory evaluation and microbiological assay showed that treatment with EW(−)/EW(+)/1%(C + T) extended the shelf-life of carp fillets to 16 and 1.3 days compared with 4 and 0.3 days for the control samples during storage at 5 and 25 °C, respectively.     

Bcl-2 relieves the trans-repressive function of the glucocorticoid receptor and inhibits the activation of CPP32-like cysteine proteases

Glucocorticoid induces apoptosis in immature lymphocytes which is inhibitable by Bcl-2. Although glucocorticoid-mediated signal transduction is well understood, the mechanism of the induction of apoptosis by the activated glucocorticoid receptor as well as the inhibition of apoptosis by Bcl-2 remains enigmatic. Here we report that overexpressed Bcl-2 relieves the glucocorticoid receptor-mediated repressive function on the AP-1 activity and completely inhibits the activation of CPP32-like cysteine proteases. In contrast, glucocorticoid receptor-mediated transactivation was not affected by Bcl-2. This suggests that glucocorticoid may induce apoptosis by repressing transactivation by AP-1 which is relieved by Bcl-2. Furthermore, we report evidence that, in contrast with CPP32-like proteases, ICE-like proteases are not involved in this apoptotic pathway.     

Fabricating high performance a-Si solar cells by alternately repeating deposition and hydrogen plasma treatment method

The performance of a p-i buffer layer in pin amorphous silicon solar cell was improved by the “alternately repeating deposition and hydrogen plasma treatment method (ADHT)”. The optical bandgap of the a-Si film was increased by hydrogen plasma treatement. The wide optical bandgap and the high photoconductive a-Si:H films without carbon could be fabricated by the ADHT method. The conversion efficiency of the solar cell with a-Si:H buffer layer was almost the same as that using an a-SiC:H buffer layer. Second, the a-Si (ADHT) films were applied to the n-i buffer layer. The insertion of a-Si (ADHT) films between the i-layer and the n-layer was effective to improve the cell performance, especially the fill factor. With the use of high performance a-Si p-i and n-i buffer layer deposited by ADHT method, a cell conversion efficiency of 12.9% was obtained.     

Self-organized dendritic patterns in the polymer Langmuir-Blodgett film

We report the formation of a self-organized dendritic pattern of nanometer thickness in polymer Langmuir-Blodgett (LB) films. Poly(N-dodecylacrylamide) (pDDA)/chloroform solution was spread on a water surface to form a stable polymer monolayer. A pDDA monolayer was deposited onto a hydrophilic silicon substrate by upward deposition from a water subphase, and a second layer was then deposited by downward deposition. The substrate with the two layers was withdrawn from a clean water surface at a high speed to form the dendritic pattern, which was imaged by atomic force microscopy. The height of the pattern, 3.5 nm, corresponds to the height of a bilayer pDDA LB film, suggesting that the pattern forms when the deposited outermost layer overturns by meniscus oscillation. A similar dendritic structure of narrower width and lower height was fabricated on a hydrophobic silicon substrate.