본 논문에서는 시간에 따라 연속적으로 변하는 3 × 3 행렬의 회전 성분을 효율적으로 추출하는 실용적인 방법을 제안한다. 이는 물리기반 동적 변형을 위하여 널리 사용되는 공회전 유한요소법이나 형상 맞춤 변형에서 매우 중요한 기술이다. 최근 극분해를 사용하는 시간 독립적인기존 방법들과 달리 회전행렬 추출을 물리적으로 공식화한 후, 점진적 회전 표현법을 이용하는반복법이 제안되었다. 본 논문에서는 점진적 회전 벡터의 최대 회전각을 π/2 이내로 제한함으로써 반복 횟수를 줄이는 최적화 기법을 개발한다. 사실적인 동적 변형 시뮬레이션에서는 충분히 작은 시간 간격을 사용하기 때문에 이러한 제한은 실용적으로 문제가 되지 않는다. 다양한실험을 통해 제안된 방법의 효율성 및 실용성을 보인다.

Background : The effective components of Omija(Schisandra chinensis Bailllon) are lignans (schizandrins and gomisins), and this components were contented mostly in seed part on Omija, which have various physiological functionalities such as anti-cancer, anti-inflammatory, and antioxidant activities. Methods and Results : This study was carried out to determine effective condition(CO2, CO2+ethanol) on extraction using supercritical carbon dioxide extraction (SFE) system and to find interrelation on effective components and antioxidant activity of extracts and residues obtained after extraction. Effective components were analysed lignans and phenolic compounds and antioxidant activirty was determined for DPPH radical scavenging ability on methanol extracts of SFE-extract and SFE-residue. On SFE with ethanol, SFE extract was separated two phase, upper(water phase) and lower(oil phase). SFE-extract showed the highest total lignans content(61.36 mg/g, 72.14 mg/g on lower, 50.58 mg/g on upper) and the lowest total phenolic compounds(6.52 mg/100g) and SFE-residue showed the lowest total lignans content(1.45 mg/g) and the highest total phenolic compounds(16.23 mg/100g) by extracted on CO2+ethanol treatment. SFE-residue methanol extract showed the highest DPPH radical scavenging abilities and SFE-extract upper showed the lowest. Conclusion : Thus, this results showed SFE-extract showed the highest total lignans content, but SFE-residue showed the highest DPPH radical scavenging ability although the lowest total lignans content.

It is important that structure's exact damage analysis and decision-making for recovery when natural disasters cause damage on SOC structure. There are many related studies using geo-spatial data like satellite and aerial images. Recently the interest has increasing about utilizing UAV(Unmanned aerial vehicle). But there are little studies related it. Therefore, we present the extraction method of the shape changes of structure damage using UAV images.

A new extraction method-heated ultrasonic extraction was qualitatively and quantitatively analyzed for the extraction of major ginsenosides from ginseng extract; this new high-performance liquid chromatography (HPLC) method was compared with the official extraction method of Korean industrial standards and standard for health functional food. Methods and Results : Ginsenoside compounds were analyzed for 35 minutes by the new HPLC analysis method using a Halo® RP-Amide column. The new HPLC analysis method was validated by the measurement of intra-day and inter-day precision, accuracy, limit of detection (LOD), and limit of quantification (LOQ) of each ginsenoside. The correlation coefficients (r2) for the calibration curves of the ginsenoside compounds were over 0.9997 in terms of linearity. The heated ultrasonic extraction method using ultrasonication for 30 minutes at 50℃ yielded higher amount of ginsenosides than the extraction method of the Korean industrial standards owing to the enhancement of extraction efficiency. Conclusions : Compared to the other extraction methods, the heated ultrasonic extraction method yielded a higher amount of ginsenoside Rb1 than Rg1 index compounds for the quality evaluation of ginseng roots.

본 연구에서는 알칼리 사용에 따른 갈변을 최소화하고 영양적으로 우수한 천마 단백질을 보다 효율적으로 추출하기 위하여 용출 및 침전 pH에 따른 단백질의 갈변도와 함량을 측정함으로써 탈지 천마 단백질 알칼리 추출의 최적pH 조건을 설정하고자 하였다. 천마의 수분은 약 15%로 측정되었으며, 대부분 탄수화물로 구성되어 있었고, 단백질의 함량이 높은 것으로 확인되었다. 이러한 단백질을 다양한 pH에서 용출시킨 결과 pH가 증가함에 따라 용출된 단백질의 양이 증가하였으며, 갈변도 또한 증가함을 보였다. 침전 pH에 따른 단백질 함량은 pH 4에서 침전된 pellet이 가장 많은 함량을 나타내었으며, 상등액의 단백질 함량 또한 대부분 pH 4로 침전시킨 경우 가장 적은 것으로 확인되었다. 뿐만 아니라 단백질의 회수율도 침전 pH가 4일 때 가장 높은 값을 나타내었다. 따라서 갈변도와 단백질 함량을 고려한 탈지 천마 단백질 추출을 위한 최적조건은 용출 pH 9와 침전 pH 4로 결정되었다.

본 연구에서는 다양한 추출방법(열수, 가압가열, 초고압 추출방법)을 통해 톳 추출물을 제조하였으며 품질특성을 실시하여 효과적인 톳 추출방법을 제시하고자 하였다. 추 출 수율은 초고압 추출물, 가압가열 추출물, 열수 추출물 순으로 높은 수율을 확인하였으며 색도의 경우 열수 추출물 에서 높은 명도와 황색도를 나타내었고 가압가열 추출물에 서는 적색도가 높았다. 추출방법에 따른 톳 추출물의 전당 함량을 측정한 결과, 전체적으로 모든 추출물이 40~60%의 높은 전당 함량을 보였으며 특히 가압가열 추출물의 함량이 높았다. 또한 시료별 전당 함량의 경우 가압가열, 열수, 초고 압 추출물의 순으로 높은 함량을 보였으며 이는 환원당과 단백질 함량에서도 동일한 결과를 나타내었다. 그러나 우 론산 및 총 아미노산 함량의 경우 초고압 추출물이 다른 추출물보다 높은 함량을 보였으며, 특히 asparagine의 경우 초고압 추출물에서만 검출되었다. 톳의 다당류 성분을 알 아보고자 에탄올을 이용하여 조다당류를 추출한 결과 수율 의 경우 초고압 추출물에서 4.75%로 높았으며 가압가열, 열수 추출물의 순으로 나타났다. 또한 high performance anion exchange chromatography를 통하여 조다당류의 구성 당을 살펴본 결과 fucose가 주 당성분인 polysaccharide임을 알 수 있었으며 galactose, glucose, xylose가 함유되어 있음 을 알 수 있었다. 이러한 결과를 종합해 볼 때 높은 온도와 압력을 가해 추출할 경우 해조류의 수율 및 유용성분의 추출이 용이해짐을 알 수 있었으며 추후 적절한 압력과 온도 설정관련 연구를 통해 해조 가공산업에 유용할 것으로 판단된다.

서북태평양에서 발생하는 태풍은 돌풍 및 강우를 동반하여 한반도뿐만 아니라 동아시아에 상당한 인적 및 물질피해를 야기함에 따라 이에 대한 수방대책 및 치수정책 수립이 시급한 실정이다. 따라서 본 연구에서는 태풍의 경로 및 규모를 고려한 태풍강우량 추출기법을 제안하고 과거 태풍 감시구역을 이용한 태풍강우 추출기법과 비교하여 적용성을 검토하였다. 태풍규모를 결정하기 위해 본 연구에서는 평균 태풍강우량을 산정하였으며, 산정결과 태풍 규모가 반경 700 km일때 평균 태풍강우량이 최대로 나타났다. 또한, 본 연구에서 제안하는 태풍의 경로 및 규모를 이용한 태풍강우량 추출기법은 과거 태풍 감시구역을 이용한 강우량 추출기법의 한계를 보완할 수 있을 것으로 판단되며, 유역별, 행정구역별로 태풍이 야기한 직접적인 강우를 추출할 수 있으며 주관적인 판단에 의해 발생할 수 있는 태풍강우의 과대 및 과소평가의 위험성을 최소화 할 수 있다. 본 연구의 결과는 향후 태풍과 집중호우의 특성분석과 기상인자를 활용한 강우예측, 수공구조물 설계, 산사태, 토석류에 대한 사전 대비책 등에 활용될 수 있을 것으로 기대된다.

A rapid and simple method for the quantitative determination of volatile fatty acids (VFAs; propionic acid, n-butyric acid, i-valeric acid and n-valeric acid) and indoles (phenol, p-cresol, 4-ethyl phenol, indole and skatole) in pig slurry and dog excrement using solid-phase micro-extraction (SPME) coupled to gas chromatography was evaluated. 50/30 ㎛ DVB/CAR/PDMS (Divinylbenzene/Carboxen/Polydimethylsiloxane) fiber was used to extract the target compounds in aqueous media. Sample amount and adsorption time was standardized for the routine analysis. Detection limits were from 0.11 to 0.15 ㎍/L for VFAs and from 0.12 to 0.28 ㎍/L for indoles and the correlations observed (R2) were 0.975～1.000. This method was applied to the pig slurry, fertilizer, compost and dog excrement. In nearly all cases, the indoles were detected in concentrations of higher than their limits of detection (DOLs). But the VFAs in swine manure were below their DOLs.

This study has been conducted to establish the optimal extraction process and HPLC analysis method for thedetermination of marker compounds as a part of the materials standardization for the development of health functionalfood materials from Astragali radix. Five extraction conditions including the shaking extraction at room temperature andthe reflux extraction at 85℃ with 30%, 50% and 95% ethanol were evaluated. Reflux extraction with 50% ethanol showedthe highest extraction yield as 27.27±2.27%, while the extraction under reflux with 95% ethanol showed significantly thelowest yield of 10.55±0.24%. The quantitative determination methods of calycosin-7-O-β-D-glucoside and calycosin asmarker compounds of Astragali radix extracts were optimized by HPLC analysis using a Thermo Hypersil column(4.6×250㎜, 5㎛) with the gradient elution of water and acetonitrile as the mobile phase at the flow rate of 0.8mL min-¹and a detection wavelength of 230㎚. The HPLC/UV method was applied successfully to the quantification of two markercompounds in Astragali radix extracts after validation of the method with the linearity, accuracy and precision. The con-tents of calycosin-7-O-β-D-glucoside and calycosin in 50% ethanol extracts by reflux extraction were significantly higher as1,700.3±30.4 and 443.6±8.4㎍ g-1, respectively, comparing with those in other extracts. The results indicate that thereflux extraction with 50% ethanol at 85℃ is optimal for the extraction of Astragali radix, and the established HPLCmethod are very useful for the evaluation of marker compounds in Astragali radix extracts to develop the health functionalmaterial from Astragali radix.

Polymerase chain reaction (PCR) is highly utilized for QTL analysis, positional cloning of valuable genes, and molecular breeding in crop science. Usually those experiments handle DNA samples of many genotypes (up to several thousands). However, many DNA extraction protocols require longer time using harmful chemicals such as chloroform, phenol, and liquid nitrogen. Here, we introduce a new DNA extraction method for PCR with agarose/PAGE analysis from a diversity panel of rice genotypes identified with yield enhancing traits. This protocol consists of four steps including injection of extraction buffer (20 mM Tris-HCl pH9.5, 200 mM KCl, 2 mM EDTA) into the tubes containing leaf tissues and steel balls, and crushing tissues using Geno-Grinder without liquid nitrogen, sample incubation at 65°C, and then centrifugation for removing cell debris. After centrifugation the crude extracts directly used as template DNA for PCR. Through this protocol we could complete F1 hybridity test from approximately 2,100 plants that come from 96 cross combinations with 13 SSR markers. In addition, we tested the DNA quality by PCR amplification of high GC-rich region and large target size (-2kb). From these results our DNA extraction method produces enough DNA quality for PCR and is suitable for large scale molecular analysis from rice plants.

This study was conducted to improve the analytical method of siloxanes in biogas. Methanol and hexane were tested as absorption solvents of the impinger absorption method, and also the hexane extraction for pretreatment of sample was evaluated. Manufactured gas contained siloxanes of 50 ppm was completely absorbed by the methanol impinger absorption. The absorption efficiency of biogas containing only 2 ppm, however, was maximum 84%. As the condensate on the first impinger increased, the absorption rate of methanol was decreased. The hexane extraction method of the sample was considered to proper the method of moisture removal. The hexane extraction result showed the high recovery factor and the low relative standard deviation. It is suggested that the suitable choice of solvent and pretreatment is required, as the analysis result of siloxane sample may be differentiated depending on the type of biogas or the sampling point.

This study was conducted to evaluate the quality and anti-oxidant characteristics of different granule tea variants (WSMGT: granule tea prepared from sea mustard hot water extract; ASMGT: granule tea prepared from sea mustard autoclave extract; WSTGT: granule tea prepared from sea tangle hot water extract; and ASTGT: granule tea prepared from sea tangle autoclave extract) from sea tangle and sea mustard powder. The Color of WSTGT showed the highest L*, b* values, and the lowest a* value. The water absorption binding agents in ASMGT were higher than those in WSMGT, WSTGT. and ASTGT. Binding agents on water absorption in ASMGT were higher than those of WSMGT, WSTGT, and ASTGT. The alginic acid content of ASMGT was highest. The total polyphenol and total flavonoid contents of ASMGT and ASTGT were highest. The electron donating ability and ferrous ion chelating activity in WSTGT greatly increased compared to those in the other granules tea variants. These results suggest that pressure extraction can be used in functional foods.

본 논문에서는 동작인식 위한 정확한 배경 분할 및 특징점 추출 방법을 제안한다. 배경 분할 과정에서는 먼저, HSV 입력 이미지를 RGB 색상 공간에서 HSV 색상 공간으로 변환한 뒤, H와 S 값에 대한 두 개의 임계치를 사용하여 살색 영역을 분할, 프레임간의 차영상을 이용하여 움직임이 있는 영역을 추출한다. 차영상에서 발생하는 잔상 영역을 제거하기 위하여 헤시안 어파인 영역 검출기를 적용하고, 잡음이 제거된 차 영상과 살색 영역의 이진화 영상을 이용하여 사람의 동작이 나타나는 영역을 분할한다. 특징점 추출 과정은 전체 영상을 블록 단위로 나눠서 각 블록 안에서 분할된 영상에 포함되는 픽셀들의 중점을 구하여 특징점을 추출한다. 실험결과 복잡한 환경에서도 정확한 배경 분할과 사용자 동작을 대표하는 특징점 추출이 약 12 fps로 가능함을 알 수 있었다.

The study of molecular markers to improve crops largely depends on the availability of rapid and of efficient DNA extraction methods. Here we developed a cheap and convenient method to isolate genomic DNA from rice grains suitable for large-scale microsatellite analysis. We confirmed that the isolated rice DNA is suitable for PCR analysis with STS marker and SNP marker, as well as microsatellite marker. Further, we established high-throughput DNA extraction system in a 96-well plate format which make it possible high-throughput analysis of microsatellite markers with rice grains. This implies that the new method could be a useful tool for other types of marker analysis in large scale.

Traditionally fatty acid composition used to be analysed by a GC and the sample preparation process includes lipid extraction from sample and subsequent methyl esters preparation, which are time-consuming and cumbersome. As an alternative, simultaneous extraction/methylation methods are being developed for rapid and simplified sample preparation. To optimize one-step extraction/methylation method for analysis of fatty acid composition in brown rice, various reaction factors such as sample to reaction solution ratio, reaction time and temperature, shaking intensity were changed and resultant fatty acid composition data were evaluated in comparison with previous reports. The ratio of sample weight to reaction solution volume was the most critical factor in that higher sample to reaction solution ratio caused overestimation of palmitic acid and linoleic acid composition, resulting in underestimation of oleic acid. Lower reaction temperature also induced overestimation of linoleic acid and underestimation of oleic acid. Reaction duration and the intensity of shaking prior to and during the reaction, however, caused no significant changes in analysis results. In conclusion, the optimum condition was mixing 5 grains (about 0.2 g) of brown rice with 680~muL of extraction/methylation mixture and 400~muL of heptane, followed by reaction at 80~circC for 2 hours.