An experiment was conducted to study effects of abomasal infusions of casein, glucose or starch on milk production and blood metabolites in dairy cows. Four lactating cows (559±41.9kg) fitted with 100 mm ruminal cannulas were used in a 4 × 4 Latin square experiment. The cows were given access ad libitum to grass silage and received 6.2 kg dry matter (DM) of a mixture of rapeseed meal (5.3kg/d DM) and barley grain (0.9kg/d DM) as a basal diet (CON), the basal diet plus intra-abomasal infusions of 270 g sodium caseinate (CAS), 300 g of glucose (GLU) or 243 g of starch (STA) starting at 09:00 h each day. Abomasal infusion of different nutrients did not affect (p>0.05) grass silage intake and rumen fermentation parameters (rumen pH, ammonia N and volatile fatty acids). As unexpected, milk yield and composition data did not differ between CON and the treated groups (p>0.05). Most of plasma amino acids were not significantly (p>0.05) affected by the abomasal infusions of CAS, GLU or STA except for histidine, tryptophan and glycine. Although histidine, known as the first limiting amino acid in dairy cows fed grass silage based diets, was significantly (p=0.003) increased by CAS, we failed to result in a clear increase in milk yield and protein yield. This discrepancy between plasma AA profiles and milk production could be presumably explained by relatively high concentration of total amino acids in the present study (2,039μmol/l).

The demand of energy is increasing around the world due to the high dependency of our society on energy. So the worldwide recognition of the limited supply of fuels has led to a large scale effort in search of alternative energy sources. Biodiesel has been considered as an alternative fuel to the petroleum diesel in compression ignition engines and is receiving more and more attention. Biodiesel can be obtained by the transesterification of methanol with triglycerides, with glycerin as by- product. This paper introduces the transesterification reaction of lard oil with methanol in the presence of hexane as solvent and potassium hydroxides as catalyst. Different from other researches, a new method to analyze the reaction process in this research was developed by starting with the by-product, crude glycerin. This new method was verified and the effects of various parameters such as solvent, molar ratio of methanol to oil (3:1-12:1), catalyst concentration (0.5-4 wt%) on the traneseterification process were investigated. Molar ratio of methanol to oil was optimized and identified to be 8:1, catalyst concentration of 2 wt% with hexane as solvent and at a temperature of 57℃ were found to be optimum for the reactions. Under this condition for 4 hours, the production yield can be 96.95%.

A survey project of TRAO with the fifteen beam array receiver system is presented. A multibeam array receiver system has been purchased from FCRAO, and is being installed on TRAO 14m telescope. The target region of the survey is from ι=120° ~137°, b=-1°~+1°, and velocity resolution would be 1 km/sec after smoothing from the original resolution of 0.64km s-1in the transition of J = 1-0 of 13CO The survey region is a part of the 12CO Outer Galaxy Survey(OGS), and would be an extension of the Bell Laboratories 13CO Galactic Plane Survey. By combining with the existing 12CO database of the Outer Galaxy Survey, we will derive physical properties of identified molecular clouds and will conduct and statistical analysis of the Outer Galalxy molecular clouds. Reduction process and analysis methods will be introduced.

The objective of this study was to examine the effect of EGF on meiotic maturation and pronuclear (PN) formation of porcine oocytes. Prepubertal gilt cumulus-oocyte-complexes (COCs) aspirated from 2~6mm follicles of abbatoir ovaries were matured in TCM199 containing 0.1mg/ml cysteine, 0.5㎍/ml FSH and LH, and EGF (0, 5, 10, 20, 40 ng/ml) for 22 hr at 39℃ in a humidified atmosphere of 5% CO2 in air. They were then cultured for an additional 22hr without hormones. In Experiment 1, to examine the nuclear maturation at 44hr of culture, the expanded cumulus cells were removed by vortexing for 1 min in 3 mg/ml hyaluronidase. The oocytes were fixed in acetic acid: methanol (1:3, v/v) at least for 48 hr and stained with 1% orcein solution for 5 min. Nuclear status was classified as germinal vesicle (GV), germinal vesicle breakdown (GVBD), prophase-metaphase I (PI-MI), and PII-MII under microscope. In Experiment 2, to investigate PN formation, oocytes were fertilized with Percoll-treated freshly ejaculated sperm (1 x10 5 cells/ml) in mTBM with 0.3% BSA and 2mM caffeine for 5hr, and cultured in NCSU-23 medium with 0.4% BSA. At 6hr of culture, the embryos were fixed in 3.7% formaldehyde for 48hr and stained with 10ug/ml propidium iodide for 30 min. PN status was classified as no or one PN (unfertilized), 2 PN (normal fertilized) and ≥3 PN (polyspermy). Differences between groups were analyzed using one-way ANOVA after arc-sine transformation of the proportional data. The rate of oocytes that had reached to PII-MII were significantly (P<0.05) higher in all groups added EGF than that of non-treated group (67%), but it did not differ among the all added groups (86%, 85%, 79% and 81%, in 5, 10, 20 and 40 ng/ml EGF, respectively). No differences on the incidence of 2PN were observed in all treated groups (25%, 30%, 33%, 29% and 29%, in 0, 5, 10, 20 and 40 ng/ml EGF, respectively), however, in non-treated group, polyspermy tended to be increased (66% vs 58%, 54%, 52% and 55%, 0 vs. 5, 10, 20, 40 ng/ml EGF, respectively). These results suggest that EGF can be effectively used as an additive for enhancing oocyte maturation and reducing the incidence of polyspermy in pig.

This study were examined whether plasminogen activators (PAs) are produced by porcine fresh or frozen-thawed cumulus-oocytes complexes (COCs) and cumulus cell free-oocytes. In fresh or frozen-thawed COCs and oocytes for 0 hour cultured, no activity of PAs was detected. However, at 24 hours of culture urokinase-type plasminogen activator (uPA) was detected in COCs and denuded oocytes. In the frozen-thawed COCs and cumulus cell free-oocytes cultured for 24 hours, no PAs were observed. After COCs were cultured for 48 hours, tissue-type plasminogen activator (tPA) and tPA-PAI were observed in COCs only. In the frozen-thawed COCs and cumulus cell free-oocytes cultured for 48 hours, no PAs were observed. These results suggest that uPA, tPA and tPA-PAI are produced by porcine COCs, but only uPA by oocytes during maturation for 24 hours. Only tPA, and tPA-PAI are produced by COCs cultured for 48 hours, and no PAs are produced by denuded-oocytes cultured for 48 hours. In all of the frozen-thawed groups, no PAs are observed by COCs and denuded-oocytes.

A characterization of the permeation and separation using single salt solution was carried out with charged composite membranes. Various charged composite membranes were fabricated by blending an ionic polymer with a nonionic polymer in different ratios. In this study, sodium alginate, chitosan and poly(vinyl alcohol) were employed as anionic, cationic and nonionic polymers, respectively. The permeation and separation behaviors of the aqueous salt solutions have been investigated through the charged composite membranes with various charge densities. As the content of the ionic polymer increased in the membrane, the hydrophilicity of the membrane increased, and pure water flux and the solution flux increased correspondingly, indicating that the permeation performance through the membrane is determined mainly by its hydrophilicity. Electrostatic interaction between the charged membrane and ionic solute molecules, that is, Donnan exclusion, was observed to be attributed to salt rejection to a greater extent, and molecular sieve mechanism was effective for the separation of salts under a similar electrostatic circumstance of solutes.

그라디오러스에 발생하는 바이러스병을 포장에서 조사한 결과 이 병율이 이었다. BYMV는 명아주에 엽맥괴사병징, 강남콩에 심한 모자익 병징 그리고 잠두에 모자익 병길을 일으켰다. CMV는 명아주에 국부병반, 담배와 오이에 모자익 병징을 일으켰다. 분류 동정된 두 바이러스는 모두 복숭아 혹진딧물에 의하여 전염되었다. 바이러스를 순화하여 흡광도를 측정한 결과 두 바이러스 모두 260nm에서 최고의 흡광도를 나타내었다. 한천내확산법을 이용한 항혈청과의 반응 결과 SDS를 처리한 BYMY와 CMV는 각각 그 바이러스의 항혈청과 뚜렷한 반응대를 형성하였다. 바이러스 입자의 진자현미경검경 과파 BYMV는 길이가 750nm였으며, CMV는 직경이 30nm이었다.