전국 4개 대도시(서울, 부산, 대전, 광주)를 중심으로 시중에서 유통되는 김밥 중 황색포도상구균의 오염도 자료와 환경조건별 미생물 변화를 예측하는 Food MicroModel^R을 활용하여 김밥 중 황색포도상구균으로 인해 식중독이 발생하지 않을 유효기간을 산정하였다. 분식점(n=79), 백화점(n=10), 편의점(n=20)으로 구분하여 분석한 여름철 평균 황색포도상구균 모니터링자료(검출률 각각 39.2%, 30%, 15%)를 시중에서 유통되는 김밥 중 황색포도상구균의 최대 섭취유효시간 산정에 활용하였으며, 모델 운영 시 김밥 중 황색포도상구균으로부터 enterotoxin이 생성되는 균수인 2×^7에 도달하는데 ℃~ 요되는 시간을 최대섭취유효시간으로 추정하였다. 하절기의 환경조건을 고려하기 위하여 ℃ 온도 조건하에서, pH, NaCl %, aw 0.99의 조건을 적용하였다. 추정된 최대섭취유효시간은 일반적인 성인이 김밥 1인분(171 g)을 섭취하는 것을 기준으로 하였을 때 구입 이후 28~30℃에서 방치할 경우 분식점은 3.9~4.6시간, 백화점 6.7~7.9시간, 편의점은 7.4~8.7시간이었다. 또한 구매한 김밥이 황색포도상구균에 기인한 식중독으로부터 안전할 최대섭취 유효시간은 99% 안전 확률에서 여름철 분식점 자료를 근거하여 30℃에서 1.9시간이었으며 15℃인 경우는 17.7시간이었다.

본 논문은 사각형 연료 탱크 내 비점성, 비압축성, 비회전 유동에 대한 슬로싱 주파수 응답의 유한요소 해석을 다룬다. 지배방정식으로 포텐셜 이론을 기반으로 한 라플라스 방정식을 적용한다. 슬로싱 운동이 작다고 가정하여 선형화된 자유표면 조건을 적용하였고, 변수분리기법을 이용하여 이론해를 구하였다. 점성 감쇠에 따른- 에너지 소산의 영향을 구현하기 위해 가상치 점성 계수를 도입하였으며, 이고 인해 공진 주파수에서 응답의 발산을 방지할 수 있나. 슬로싱 응답의 최대 진폭을 예측하기 위해 9절점 요소를 사용한 유한요소법을 이용하여 해석하였다. 슬로싱 높이, 유체 내부 동수압 및 내부 유체력의 수치 결과는 이론해와 잘 일치하였다. 유한요소 시험 프로그램을 검증한 후, 유체높이에 따른 슬로싱 주파수 응답 특성을 분석하였다.

본 논문에서는 2차원 사각탱크내 비압축성, 비점성, 비회전 유동에 대한 비선형 슬로실 해석을 다룬다. 유체영역의 지배방정식으로 포텐셜 이론에 기반을 둔 라플라스 방정식을 사용한다. 대변형의 슬로싱 거동을 표현하기 위하여 베르누이 방정식으로부터 유도된 운동 및 동역학적 자유표면 경계조건을 적용한다. 이러한 비선형 슬로싱 문제는 9결점 요소를 사용한 유한요소법에 의하여 해석되어 진다. 경계조건에 대한 시간적분과 정확한 속도계산을 위하여 각각 예측자-수정자 기법 및 최소자승법을 도입하였다. 또한, 자유표면 추적에서 야기되는 안정성 문제는 시간변동에 대한 자유표면 위치를 직접 계산함으로써 확보할 수 있었다. 외부 조화가진에 대한 본 논문의 결과는 선형이론해 또는 참고문헌의 결과와 비교하여 매우 정확하고 안정적이었다. 프로그램 검증 후, 유체높이와 가진크기에 대한 슬로싱 응답특성을 분석하였다.

본 논문은 배플을 설치한 수평으로 놓인 원통형 탱크내 슬로싱 고유진동에 대한 유한요소 해석을 다룬다. 지배방정식으로 포텐셜 이론을 기반으로 한 라플라스 방정식을 적용한다. 이 문제를 선형의 등매개 요소를 적용한 유한요소법을 이용해 해석한다. 탱크와 배플은 강체로 가정하였으며, 배플의 효과 구현은 배플의 설치 위치에 절점을 두 개로 분리함으로써 얻을 수 있다. 고유주파수와 고유모드의 추출을 위하여 Lanczos 변환법 및 Jacobi 반복법을 도입하였다. 종진동과 횡진동 모드에 대한 수치 해석결과가 참고 문헌과 비교해 볼 때 잘 일치함을 알 수 있었다. 또한 유체 높이, 배플 개수, 내공 크기, 배플 위치 등의 파라메트릭 해석을 통하여 슬로싱 특성 및 링형 배플의 영향을 고찰하였다.

2000년 국내 식중독발생 통계에 따르면, 원인식품별 식중독발생건수는 육류 등이 27.9%, 어패류 및 가공품이 26.0%, 복합조리식품(김밥, 도시락)이 24.0%의 비율을 차지하고 있으며, 원인균별 식중독발생건수는 Salmonella spp가 28.8%로 1위, Vibrio parahaemolyticus가 13.5%로 2위, Staphylococcus aureus가 8.7%로 3위를 차지하고 있다. 이에 본 연구에서는 김밥 중 황색포도상구균에 대한 분포도조사 및 오염정도를 분석하여 위해도평가의 기초자료로 활용하고자 하였다. 서울, 부산, 대전, 광주의 백화점, 편의점, 분식점 등에서 구입한 김밥 총 214건에 대한 황색포도상구균의 정량 및 정성실험 결과, 균검출율은 34.1%였고, 평균균량은 623 cfu/g이었다. 분리균에 대한 enterotoxin 실험결과 A type 42.5%(31주/73주), B type 4.1%(3주/73주), D type 2.7%(2주/73주)의 분포를 보였다. 또한 유통·판매형태별로는 분식점의 검출율이 42.8%로 백화점(25.8%) 및 편의점(12.3%)보다 높게 나타났으며, 계절별 평균균검출율은 비슷하였으나, 정량검사결과 여름철(793 cfu/g)에 겨울철(446 cfu/g)보다 균량이 1.8배 높게 나타났다.

Organic Electroluminescent devices(OELD) consisted of multilayer structures have been studied for the application the application to flat-panel display. Metal-chelate complexes, zinc bis(2-(2-hydroxyphenyl)benzoxazolate) (Zn(BOX)2) and zinc bis(2-(2-hydroxyphenyl)benzothiazolate) (Zn(BOX)2), have been intensively investigated as an white-light emitting layer and recognized to have good electroluminescent(EL) properties. In this study, (Zn(BOX)2) and (Zn(BTZ)2) were synthesized and characterized by FT-IR, 1H-NMR, UV-VIS and PL. Their EL properties were also studied and their ionization potential(IP) and electron affinity(EA) were also measured by cyclic voltammetry(CV).

본 연구는 토양근권제한이 멜론의 수량과 품질에 미치는 영향을 구명하고자, 격리상, 간이근권제한시트 및 관행 토양재배의 3가지 재배방법을 적용하여 멜론을 4월19일 부터 7월 17일까지 재배하였다. 지온은 격리상재배가 토양재배와 근권제한시트 재배보다 다소 높게 유지되었고 멜론의 생육은 토양과 근권제한시트재배에 비해 격리상 재배에서 빨랐다. 과실크기는 토양, 격리상 및 근권제한시트재배 순이었으나 당도 및 네트형성은 격리상재배가 토양재배에 비해 우수하였다. 수확기 경엽의 시들음주율은 토양재배 26.7%, 근권제한시트재배 25% 발생한 데 비해 격리상재배는 3.3%로 가장 낮았다 따라서 상품과 수량은토양재배에 비해 격리상재배에서 많았다.

This study was to determine the effect of ionomycin and 6-dimethylaminopurine (6-DMAP) and/or elcetrical stimulation on the oocyte activation and production of rabbit nuclear transplant embryos. The oocytes were collected from the oviduct of superovulated rabbits at 14 h post hCG injection and cultured in TCM-199 containing 10% FBS until 19 h post hCG injection. To determine the optimum concentration and exposure time of 6-DMAP, some oocytes were activated with 5 M ionomycin for 5 min and then in 2.0 mM 6-DMAP for 0.5 to 3.0 h, or in 1.0 to 3.0 mM 6-DMAP for 2.0 h. Other control oocytes were stimulated electrically(3X, 1.25 kV/cm, 60 sec) in 0.3 M mannitol solution supplemented with 100 M CaCl and MgCl. The nuclear donor embryos of 8-cell stage were synchronized to G phase of 16-cell stage, and the recipient cytoplasms were obtained from removal of the first polar body and a portion of membrane bound cytoplasm of the oocytes collected at 15 h post hCG injection. A separated blastomere was injected into the perivitelline space of the enucleated oocytes. The oocytes injected with nucleus were cultured until 19 h post hCG and then electrofused and activated by electrical stimulation with or without ionomycin and 6-DMAP. These nuclear transplant embryos were cultured in TCM-199 containing 10% FBS in 39˚C, 5% CO2 incubator for 120 h. For the oncytes activated parthenogenetically with electrical stimulation with or with-out ionomycin and the various concentration of exposure time of 6-DMAP, the highest cleavage(92.3%) and development to blastocyst stage(41.0%) were resulted from the oocytes activated by ionomycin and 2.0 mM 6-DMAP for 2.0 h, which were found to be significantly(P<0.05) higher than the cleavage(45.2%) and developement to blastocyst stage(14.3%) from the oocytes activated with electrical stimulation. The significantly(P<0.05) more oocytes(71.4%) developed to 4 cell stage at 24 h post activation by ionomycin and 6-DMAP than those by electrical stimulation(18.9%). For the nuclear transplant embryos, the cleavage rate was similarly high in oocyte activation by electrical stimulation with(79.4%) or without ionomycin and 6-DMAP(70.5%). However, the embryo development to blastocyst stage was significantly(P<0.05) higher in oocyte activation by electrical stimulation with ionomycin and 6-DMAP(44.4%) than by electrical stimulation only(25.0%). The significantly(P<0.05) more nuclear transplant embryos(45.6%) developed to 4 cell stage at 18 h post activation by electrical stimulation with ionomycin and 6-DMAP than those by electrical stimulation only(10.6%). These results indicated that the supplemental oocyte activation by ionomycin and 6-DMAP with electrical stimulation enhanced and accelerated the preimplanted in vitro development of the rabbit nuclear transplant embryos.

To improve the efficiency of production of cloned embryos and animals by nuclear transplantation in the rabbit, the effect of cell cycle of donor nuclei and type of recipient cytoplasm on the in vitro developmental potential and production efficiency of offspring was determined. The embryos of 16-cell stage were collected from the mated does at 48h post-hCG injection and they were synchronized to G phase of 32-cell stage. The oocytes collected at 14h post-hCG injection were freed from cumulus cells and then enucleated. One group of the enucleated cytoplasms was activated by electrical stimulation prior to injection of donor nucleus, and the other group was not pre-activated. The separated Gphase blastomeres of 32-cell stage embryos were injected into the perivitelline space of recipient cytoplasms. After culture for 20h post-hCG injection, the nuclear transplant oocytes were electrofused and activated by electrical stimulation and the fused nuclear transplant embryos were co-cultured for 120h and the nuclear transplant embryos developed to blastocyst stage were stained with Hoechst 33342 dye and their blastomeres were counted. Some of the nuclear transplant embryos developed in vitro to 2- to 4-cell stage were transferred into the oviducts of synchronized recipient does. The electrofusion rate was similar between the types of donor nuclei and recipient cytoplasms used. However, the nuclear transplant embryos using G phase donor nuclei were developed to blastocyst at higher rate(60.3%) than those using S phase ones(24.7%). Also, when non-preactivated oocytes were used as recipient cytplasms, the develop-mental rates of nuclear transplant embryos to blastocysts were significantly(P< 0.05) higher(57.1%) than those using preactivated ones(20.8%). The cell counts of nuclear transplant embryos developed to blastosyst stage were increased signficantly(P<0.05) more in the non-preactivated recipient cytoplasm(163.7 cells), as compared whit the preactivated recipient cytoplasm(85.4 cells), A total of 49 nuclear transplant embryos were tranferrid into 5 recipient does, of which two offsprings were produced from a foster mother 31 days after embryo transfer. these results showed that the blastomeres of G1 phase and non-preactivated oocytes might be utillzed efficiently as donor nuclei and recipient cytoplasms in the nuclear transplant procedure, thought the offspring production remained still low.

(1-x)CaTi O3-xLa(Z n12/ Ti12/) O3의 마이크로 유전특성을 조사하였다. x가 증가함에 따라 비유전율과 공진주파수의 온도계수는 감소하였으며, Qㆍ f0는 증가하였다. 그 결과 x=0.5인 (C a0.5L a0.5)( Ti0.75Z n0.25) O3의 조성에서 εr=51, Qㆍ f0=38,000 (at 7 GHz), τf=+5ppm/˚C의 유전특성이 나타났다. (C a0.5L a0.5)( Ti0.75Z n0.25) O3조성의 소결온도를 저하시키기 위하여 B i2 O3를 주조성으로한 소결체를 첨가하여 소결 및 유전특성을 조사하였다. 1wt% 0.76B i2 O3-0.24NiO가 첨가된 경우 소결온도는 150˚C 낮아졌으며, 비유전율 (εr), 공진주파수의 온도계수(τf), Qㆍ f0가 각각 50+5ppm/˚C, 35,000인 마이크로파 유전특성이 얻어졌다. 또한 3wt%의 0.76B i2 O3-0.24NiO가 첨가된 경우 소결온도는 200˚C 저하되었고, 비유전율 (εr)과 공진주파수의 온도계수 (τf)는 변하기 않았으나, Qㆍ f0값이 38,000에서 25,000으로 저하되었다. 25,000으로 저하되었다.되었다.되었다.되었다.

This study was carried out to determine the effect of bovine follicular fluid(bFF), hormones, and fetal bovine serum(FBS) supplemented in the medium on the in vitro fertilization and development of bovine embryos. The ovaries were obtained from a local abattoir and placed in physiological saline kept at 30~32˚C and brought to the laboratory within 3~4 hours. The oocytes and follicular fluid were collected by aspiration from visible follicles, and the oocytes of grades I on the basis of the morphology of cumulus cells attached and the homogeneity of cytoplasmic granules were selected and used for maturation. The basal media used for oocyte maturation, fertilization and embryo development in vitro were Ham' F-10, TALP and TCM-199, respectively. The hormones supplemented in maturation medium were consisted of 35 pg /ml FSH, 10 pg /ml LH and 1 pg/mi estradiol-l7. The bFF collected from 5~9 mm follicles was centrifuged, filtered and inactivated by heat-treatment at 56˚C for 30 min. FBS also was inactivated with the same method and kept at -20˚C until use. The embryos were co-cultured with the monolayer of bovine oviductal epithelial cells at 39˚C under 5% in air for 9 days. The results obtained were summarized as follows: The fertilization rate of oocytes was found 87.4% from 10% FBS and hormones treatment for IVM, and 37.1% of these TVF embryos were developed to blastocyst stage in 10% FBS groups. Compared with this control system, the fertilization rate was decreased significantly(P<0.05) in the maturation without either FBS or hormones. These IVF embryos were developed to morula stage at the similar rate, but to blastocyst at significantly(P<0.05) lower rate in the embryo culture with or without FBS supplementation. The fertilization rate(82.9%) in hormones and 10% inactivated bFF was similar with 10% FBS and hormone groups(87.4%), but decreased significantly(P<0.05) in 20 or 30% bFF (61.0 or 66.0%), respectively. In vitro developmental competence to blastocyst stage in 10% FBS and 20% inactivated bFF(37.1% and 31.4%) was higher than in 10 or 30% inactivated bFF(20.0 or 19.2%) or 10, 20 and 30% fresh bFF(19.1, 21.0 and 17.5%) The results indicated that the in vitro fertillzation and development rate of the embryos should be improved in 10% FBS or 20% inactivated culture system and 20% inactivated bFF might be available economically for bovine oocyte maturation and embryo culture instead of fetal bovine serum.

To improve the efficiency of in vitro production of embryos with follicular oocytes in Korean Native cows, the recovery rates, in vitro maturation, fertilization and development, and the time required for collecting and processing oocytes by aspiration with or without slicing were evaluated comparatively. The ovaries were obtained from a local abattoir and placed in physiological saline at 25~28 and brought to the laboratory within 3 hrs. The oocytes were collected by aspiration of follicles(2~6mm) with or without slicing ovaries after aspiration, and classified into Grade I, Grade II, Denuded, Expanded oocytes by the morphology of cumulus cells attached and the homogeneity of cytoplasmic granules. Also the time required for each step of collecting and processing oocytes were measured. The cumulus cells were removed in some Grade I oocytes to measure their size and nuclear configuration before and after in vitro maturation. The Grade I oocytes were matured in vitro(IVM) for 24 hrs. in TGM-199 supplemented with 35g /ml FSH, 10g /ml LH, 1 g /ml at 39 under 5% C02 in air. They were fertilized in vitro(IVF) by epididymal spermatozoa treated with heparin for 24hrs. and then the zygotes were cocultured in vitro (IVC) with bovine oviductal epithelial cells for 10 days. The results obtained were as follows: The number of oocytes recovered per ovary was averaged 6.6 by aspiration and 11.2 by slicing post aspiration, which summed to 17.8. The number of Grade I oocytes recovered per ovary was averaged 3.1 by aspiration and 3.6 by slicing, which summed to 6.7. The percentage of Grade I to total oocytes recovered was significantly(P<0.05) higher as 48.0 % in aspiration than 31.6% in slicing post aspiration. The time requlred for recovering a Grade I oocyte by aspiration and slicing was 1.1 and 2.5 min, respectively. The mean diameter of Grade I oocytes by aspiration and slicing was similar as 148.7 and 151.5m, respectively. The percentage of Metaphase II stage oocytes after IVM for 24 hours was significantly (P