Influence of death struggle on the structural changes in chub mackerel muscle during chilled storage

ABSTRACT: Chub mackerel (34–35 cm, approximately 500 g), which were caught by fishing with a rod and line at the Bungo Channel, Oita prefecture, were rested overnight in a fish preserve and either killed by decapitation (control group) or allowed to struggle in air for 30 min (struggled group). Muscle samples were excised every 4 h, and measurements on breaking strength and histological observations were done for both groups. The breaking strength of muscle in the control group was significantly higher than that in the struggled group, whereby a decrease in breaking strength was delayed for 12 h compared to the struggled group. Light microscopy showed space extension among muscle cells in association with a decrease in breaking strength. Especially in the struggled group, the extended area was larger and the difference in area was significant at the time when breaking strength showed a significant difference. Using electron microscopy, the extended area showed cut and/or disappeared collagen fibrils. From these results, it was demonstrated that struggling to death promoted the degradation of collagen fibrils and the weakening of connective tissue and, resultantly, led to the faster softening of muscle of chub mackerel.     

A short discussion on the chemical composition of allophane based on the data of Yoshinaga in 1966

Many scientists have attempted to discern the chemical composition and the structure of allophane (2, 4–6). Yoshinaga (7) presented the chemical composition of eighteen samples of pure allophane in detail, and concluded as follows: All samples consisted principally of silica, alumina, and water. The silica-alumina molecular ratio ranged from about 1.3 to 2. Molecular ratios of ignition loss (+H₂0) and total water (±H₂O) to alumina were nearly constant, with the averages about 2.5 and 5.7, respectively. The chemical composition of soil allophane fell into a relatively narrow range, and the change in the percentage composition of the three major elements had a regularity.     

Autoimmune disease and impaired uptake of apoptotic cells in MFG-E8-deficient mice

Apoptotic cells expose phosphatidylserine and are swiftly engulfed by macrophages. Milk fat globule epidermal growth factor (EGF) factor 8 (MFG-E8) is a protein that binds to apoptotic cells by recognizing phosphatidylserine and that enhances the engulfment of apoptotic cells by macrophages. We report that tingible body macrophages in the germinal centers of the spleen and lymph nodes strongly express MFG-E8. Many apoptotic lymphocytes were found on the MFG-E8-/- tingible body macrophages, but they were not efficiently engulfed. The MFG-E8-/- mice developed splenomegaly, with the formation of numerous germinal centers, and suffered from glomerulonephritis as a result of autoantibody production. These data demonstrate that MFG-E8 has a critical role in removing apoptotic B cells in the germinal centers and that its failure can lead to autoimmune diseases.     

Formation of methyl mercaptan in paddy soils I

It is well known that methyl mercaptan is porduced by the microbiological decomposition of methionine1),2),3). According to Kondo ⁴⁾ and Onitake ¹⁾not only hydrogen sulfide, but also methyl mercaptan were produced from cystine by E. coli and Proteus vulgaris in the medium containing one of glucose, lactose, sucrose, glycerin or histidine. Moreover, Onitake ¹⁾ found that methyl mercaptan was produced by the action of E. coli in the medium containing hydrogen sulfide and a trace of ethyl alcohol, and that evolution of methyl mercaptan began only 5 minutes after the start of experiment in the medium containing methionine, but it began after 12hrs in the medium containing 1-cystine and glucose. According to Birkinshaw, Findlay and Webb⁵⁾ methyl mercaptan was found in the medium containing glucose, sulfate and other mineral salts, inoculated by Schizophyllum commune. In the same cultural condition as given above, methyl mercaptan, dimethyl sulfide, and dimethyl disulfide were detected by Challenger and Chartons ⁵⁾ from the data presented above, in addition to microbiological formation of methyl mercaptan from methionine, the possibility cannot be excluded of methyl mercaptan formation by microbes from cystine, sulfate or hydrogen sulfide in the medium containing one of organic compounds such as sugars, glycerin, histidine and ethyl alcohol, etc.     

Photoautotrophic cultivation of oleaginous microalgae and co-pelletization with filamentous fungi for cost-effective harvesting process and improved lipid yield

Oleaginous microalga Scenedesmus obliquus SIT06 was selected as potential biodiesel feedstocks due to its high lipid content and suitable fatty acid composition for production of biodiesel with high oxidative stability and high cetane number. The important factors for cultivating microalgae in photoautotrophic mode were optimized through response surface methodology (RSM). The highest microalgal biomass obtained was 1.99?±?0.12 g L^?1 with a high lipid content of 40.86?±?0.32%. To simplify harvesting process of microalgal cells, pellet-forming filamentous fungi were inoculated into the late log-phase of microalgae culture. Among the fungi tested, Cunninghamella echinulata TPU 4652 most effectively harvested the microalgal cells with the highest flocculation efficiency of 92.7%. Moreover, the biomass and lipids of microalgae-fungi pellets were as high as 4.45?±?0.06 and 1.21?±?0.08 g L^?1, respectively. The extracted lipids were mainly composed of C16:0, C18:0, and C18:1, and their estimated fuel properties meet with the international standards indicating their potential use as biodiesel feedstocks. This study has shown the strategies not only to simplify the harvesting process but also to increase the lipid yield and tailor the lipid composition.     

The effectiveness of a new physical property evaluation method of kamaboko which applied the principal component analysis to the puncture and stress relaxation tests

ABSTRACT:   The physical properties of 49 commercial kamabokos were measured by the puncture and stress relaxation tests. The principal component analysis was applied to the physical parameters of both tests, and their cumulative contribution ratios were over 90% with the first and second principal components, respectively. The comparison among the kamabokos was carried out using the synthetic physical parameters. The kamabokos produced in same area showed the peculiar distribution. The relative positional relation of kamabokos measured by the stress relaxation test was different from that by the puncture test for many of the kamabokos. Physical property evaluation using a principal component analysis is very effective for intensiveness of many measurement parameters. If much more kamabokos were measured by this method, regional characteristics of kamabokos would be clarified.     

Evaluation of coral bleaching condition <Emphasis Type="Italic">in situ</Emphasis> using an underwater pulse amplitude modulated fluorometer

ABSTRACT:   Photosynthetic activities of hermatypic corals (28 genera, c . 68 species and c. 92 specimen) were measured in November 2000 at Sekisei lagoon, Okinawa, Japan, using an underwater pulse amplitude modulated fluorometer. Maximum quantum yield (Fv/Fm) ranged from 0.61 to 0.70 and had an average value of 0.664 (standard deviation [SD], 0.0289). Following the measurement of Fv/Fm, quantum yield (Fm'-F)/Fm' at eight-leveled actinic-light intensities were obtained from all specimens. Values of electronic transport rates (ETR) were nearly the same under low photosynthetic active radiation (PAR; µmol quanta/m² per s) condition and varied with increasing PAR. The value of ETR at 100 µmol quanta/m² per s ranged from 21.3 to 30.0 and had an average of 27.8 (SD, 2.09). In August 2001, a coral bleaching event was observed in Sekisei Lagoon. During the event, photosynthetic activities of 21 specimens of eight species (seven genera) were measured. By applying two indicators, Fv/Fm and ETR at 100 µmol quanta/m² per s obtained in August 2000, 18 of 21 specimens were suggested under the bleaching process. In case of Porites lutea , seven colonies were visually evaluated for their condition of bleaching and were found to have two 'normal', three 'slightly bleached' and two 'heavily bleached'. From the density of zooxanthellae, colonies evaluated 'normal' or 'slightly bleached' did not show an apparent difference. However, they were clearly identified by Fm/Fv and ETR at 100 µmol quanta/m² per s.     

Extended glucuronidation is another major path of cyanidin 3-O-beta-D-glucopyranoside metabolism in rats

We previously determined that five rather hydrophobic metabolites appeared in blood plasma after oral administration of cyanidin 3-O-beta-D-glucopyranoside, but a group of hydrophilic metabolites still remained unidentified. In the present study, 12 hydrophilic metabolites found were collected from urine and plasma samples by high-performance liquid chromatography (HPLC) and then analyzed by tandem MS spectrometry. From the MS spectra, four metabolites out of 12 were assigned as glucuronides of cyanidin 3-O-beta-D-glucopyranoside and six out of 12 were glucuronides of the primary metabolites of cyanidin 3-O-beta-D-glucopyranoside (O-methyl cyanidin 3-O-beta-D-glucopyranoside). Extended glucuronides of cyanidin 3-O-beta-D-glucopyranoside and O-methyl cyanidin 3-O-beta-D-glucopyranoside showed their maximum plasma concentrations at 15 and 60 min (or 30 min) after oral administration, respectively. Their maximum plasma concentrations ranged from 15 to 70 nM. From the profile of urinary-excreted anthocyanins after intravenous administration, it was deduced that extended glucuronides of cyanidin 3-O-beta-D-glucopyranoside and O-methyl cyanidin 3-O-beta-D-glucopyranoside were mainly produced in the liver rather than by intestinal flora. The area under the plasma concentration curve was 0.25 micromol min/L for extended glucuronides of cyanidin 3-O-beta-D-glucopyranoside and 0.14 micromol min/L for O-methyl cyanidin 3-O-beta-D-glucopyranoside, respectively, when evaluated as cyanidin 3-O-beta-D-glucopyranoside equivalent, indicating that extended glucuronidation is a critical pathway in cyanidin 3-O-beta-D-glucopyranoside metabolism in rats.     

Cadmium contamination of soils and rice plants caused by zinc mining IV. Use of soil amendment materials for the control of Cd uptake by plants

In view of the difficulty in practicing water management as a measure to prevent the production of high Cd rice, alkaline or calcareous soil amendment materials were examined, concerning their pH effect on the availability of soil heavy metals.

1. In the experiment conducted on the contaminated paddy field, the essential Cd uptake by the plant occurred after the ear-forming stage and was reduced remarkably by a basal application of the amendment materials followed by top application, depending on the activity of raising the soil pH. Combined use of calcium silicate and fused magnesium phosphate for a basal dressing was most effective on Cd uptake, producing rice of the lowest Cd content, one fifth of the control.

2. The content of Cu in rice also decreased with the treatment to an extent second to Cd, while that of Zn and Pb decreased in straw but hardly changed in rice. Cu seemed fastest in the straw-to-grain movement which was also promoted by the treatments.

3. Soil Cd and Cu were less soluble in 0.1 N HCl solutions than were Zn and Pb, with the application of fused phosphate. Soil Cd became more insoluble in the incubated soil in a submerged condition and its solubility appeared to be depressed by the addition of ammonium sulfate.

4. Based on the good results for the control of high Cd rice obtained through three years' survey in the problem area, it was recommended that these materials be used in sufficient quantity to raise soil pH, taking care not to cause delay in the first growth.     

Studies on organic acids in paddy field soils with reference to their inhibitory effects on the growth of rice plants

Many Studies (1) have been made on the physiological diseases of rice plants caused by root rot which develops during the plant growth. The view that organic acids; accumulatted in rice paddy soil may be one of the factors impeding the function of roots began only recently to be expressed concerning the low productive paddy fidds. However, studies on the metabolism of these organic acids, especially of saturated lower fatty acids, are mostly fragmental except for a series of studies made by Takai and others (2). To deal with the problem of root injuries and diseases of rice plants, we must establish the magnitude of the organic acid production in relation to the differences in character of soils.