• 분석과학
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• 제30권4호
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• pp.205-212
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• 2017

Rice endosperm, the portion that remains after milling, is the part of the rice seed that is primarily consumed as a source of nutrients. There have been many studies on polysaccharides, such as hemicellulose, cellulose, and pectins, derived from the cell walls of various plant groups. It has been reported that the acidic polysaccharide fractions, which contain water-soluble pectins that have been shown to have pharmacological effects in vivo and in vitro, have common chemical structures that include galacturonic acid polymers, rhamnose, arabinose, and galactose. However, few studies have been conducted on the acidic polysaccharides contained in the endosperm of rice. In this study, we quantitatively compared the differences in the acidic polysaccharide contents from samples from two of the main varieties of rice consumed as staple foods, japonica and indica, using a colorimetric method. Rice samples were collected from 39 different regions in Korea, China, Thailand and Vietnam. Acidic polysaccharide fractions were obtained by precipitation of the alcohol-insoluble residue (AIR) and enzyme treatment of each sample. The total amount of carbohydrates and uronic acid in each acidic polysaccharide fraction were measured using the phenol-sulfuric acid method and the carbazole-sulfuric acid method, respectively. The differences in the total polysaccharide contents in the acidic polysaccharide fractions were not statistically significant (p = 0.07), but the uronic acid contents were significantly different between the two groups (p = 0.04).

• 대한화장품학회:학술대회논문집
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• 대한화장품학회 2003년도 IFSCC Conference Proceeding Book I
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• pp.590-600
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• 2003

The matrix metalloproteinases (MMPs) are a family of enzymes responsible for degrading connective tissue. MMPs catalyze the breakdown of collagen from the extracellular matrix, leading to wrinkle formation and accelerated skin aging. Furthermore, ultraviolet irradiation causes increased expression of certain MMPs. In the extracellular matrix turnover, MMPs are interacting with endogenous regulators named tissue inhibitors of metalloproteinases (TIMPs). Using peptide substrate assays, it has been demonstrated that TIMP-MMP complexes interact highly specifically with $K_{i}$ values of 10$^{-9}$ -10$^{-16}$ M. Therefore applications for TIMP as inhibitor of collagen degradation are suggested for cosmetic anti-aging products to prevent wrinkle formation and loss of elasticity. To date four TIMP proteins (TIMP-1, TIMP-2, TIMP-3 and TIMP-4) have been identified which show a high degree in sequence similarity. The production of human TIMP-2, a 194-residue nonglycosylated protein, was performed by fed-batch culture of Escherichia coli. TIMP-2 accumulated in the bacterial cells in an insoluble form as inclusion bodies. The inclusion bodies were solubilized and the protein refolded to yield the native TIMP-2 in the active form. The integrity of the protein was confirmed by mass analysis, Edman sequencing and gel shift experiments with authentic samples. The inhibitory activity of the refolded and purified TIMP-2 was demonstrated with MMP-1 and MMP-2 assays using synthetic fluorogenic peptide substrates.s.

• 약학회지
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• 제1권1호
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• pp.2-4
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• 1948

Syringa oblata var dilatata (Nakai) Rehder is a oleaceous, deciduous shrub indigenous in the calcareous zones of Korea. The author researched the constituents of the leaves of the plant, especially the bitter principles which may be used as amara. According to the literature a bitter principle Syringin and Mannitol were isolated from the leaves of S. vulgaris L. And later on B. Power indicated that syringin and mannitol were widely distributed in oleaceous plants. The fresh leaves of the plant wer extracted with hot water, the filtered clear liquid was mixed with solution of lead acetate. The lead precipitate was filtered off and the filtered liquid was freed from lead by H$_{4}$S. The filtrate thus obtained was evaporated, and from the residue colorless needles, M. P. 166.deg., were obtained. It was soluble in water, in hot alcohol, and insoluble in ether and had a sweet taste. The results of the elementar analysis, M. P. and other characteristics agreed with that of d-mannitol. Finally it was proved to be identical with d-mannitol through conversion of it into Hexaacetyl mannitol, M. P. 124.deg., Triformal mannitol, M. P. 227.deg., Tribenzal mannitol, M. P. 224.deg., which exhibited no depression, when mixed with authentic specimens. The experiments to isolate bitter principles of the plant are in progress.

• Preventive Nutrition and Food Science
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• 제11권1호
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• pp.10-16
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• 2006

Radical scavenging and antioxidant activities of Laminaria japonica and fermented its extracts were evaluated. Freeze-dried L. japonica was fermented by Aspergillus oryzae and extracted with distilled water. The extract solution was mixed with ethanol and centrifuged. The supernatant was ethanol soluble fraction, non-polysaccharide fraction (ESF), and residue was ethanol insoluble precipitation, polysaccharide fraction (EIP). ESF was subjected to sequential fractionation with dichloromethane, ethyl acetate, butanol and water. To determine the radical scavenging and antioxidant activities of these, DPPH radical, hydroxyl radical, superoxide anion radical scavenging activities and linoleic acid oxidation were tested. Among the extracts, ESF of fermented L. japonica showed the highest radical scavenging activity. The ESF showed DPPH radical scavenging activity of 64.33% at concentration of $50{\mu}g/mL$. It was higher than 57.70% of vit. C. Ethyl acetate and butanol fraction had high value of radical scavenging and antioxidant activities, especially butanol fraction of fermented L. japonica was 79.48 % of hydroxyl radical scavenging activity at concentration of $50{\mu}g/mL$. The fermented L japonica had radical scavenging and antioxidant activities higher than L. japonica. These results suggest that fermented L japonica is healthy food having radical scavenging and antioxidant activities.

• BMB Reports
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• 제28권6호
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• pp.477-483
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• 1995

The recombinant human interferon alpha 2a ($rhIFN-{\alpha}2a$), expressed in Saccharomyces cerevtsiae, was purified from insoluble aggregates. The inclusion body of $rhIFN-{\alpha}$ was solubilized by guanidine salt in the presence of disulfide reducing agent. The refolding of denatured $rhIFN-{\alpha}2a$ was achieved by simple dilution. The authentic interferon alpha, which has two correctly matched disulfide bonds, was seperated from incompletely oxidized $IFN-{\alpha}$ and dimeric $IFN-{\alpha}$ by use of a CM-Sepharose column, followed by size exclusion columns at two different pH conditions. The purified protein has been subjected to detailed physicochemical characterization including sequence determination. Unlike other $rhIFN-{\alpha}2a$ from E. coli reported, the $rhIFN-{\alpha}2a$ from S. cerevisiae has no methionine residue at its N-terminus originating from the start codon, ATG. The pI of the protein was determined to be 6.05 with a single band in the pI gel, which demonstrated that the purified $rhIFN-{\alpha}$ was homogeneous. The structural study using circular dichroism showed that the protein retains its three dimensional structure in the wide range of pH conditions between pH 3 and 9, and only minor strucural deformation was observed at pH 1.0.

• 한국식품과학회지
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• 제29권4호
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• pp.648-656
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• 1997

두유박을 수용성 식이섬유의 원료로 활용하기 위하여 $140^{\circ}C,\;150^{\circ}C$ 및 $160^{\circ}C$에서 각각 열처리를 통해 두유박 식이섬유의 대부분을 차지하는 불용성 식이섬유를 수용성 식이섬유로 변환시킨 후 이를 추출하여 각추출물의 이화학적 특성을 분석하였다. 각 온도별로 pH와 열처리 시간을 달리하여 추출하였을 때 최대 가용화 조건에서 수용성 식이섬유 함량은 $30.3{\sim}32.2%$이었다. 두유박 식이섬유 고온 추출물의 당 조성을 HPLC로 분석한 결과 glucose > galactose > arabinose + fucose > mannose의 순으로 많이 함유되어 있었다. 추출물을 high performance size exclusion chromatography로써 평균 분자량에 따라 3가지 획분으로 나누어 분석하였는데, 추출 온도가 증가함에 따라 고분자량 획분이 줄어들고 중간분자량 획분이 증가하는 경향을 보였다. 추출물을 함유한 용액의 점도는 추출 온도의 상승에 따라 감소하였으나, pH에 따른 변화 경향은 뚜렷하지 않았다. 추출물의 용해도는 온도가 상승함에 따라 급격하게 증가하였으며 추출 온도가 높을수록 증가하는 경향을 나타내었다. Ca-binding capacity는 $140^{\circ}C$ 추출물이 다른 시료에 비해 월등히 높았다.

• 분석과학
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• 제11권3호
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• pp.189-193
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• 1998

조사후 핵연료의 용해실험 다음에 잔류된 불용성 잔유물을 구성하는 Mo, Ru, Rh 등의 원소로 이루어진 이성분계 합금인 $MoRu_3$와 $MoRh_3$을 아르곤 아아크로를 이용하여 $1700^{\circ}C$ 이상의 고온에서 합성하였다. 이들 합금의 정확한 구조와 결정격자상수는 ICDD(International Centre for Diffraction Data)에서 제작되는 분말회절수집철(JCPDS files) 등에 수록된 바가 없다. X선 회절분석결과 이들 두 합금은 육방밀집구조와 $P6_3/mmc$의 공간군을 갖는 $WRh_3$의 구조와 매우 유사한 것으로 나타났다. 이 화합물들의 격자상수, a와 c는 최소자승법을 이용하여 구하였다. 또한 XPS로 분석을 통하여 이들의 표면을 조사한 결과 금속 표면이 실온에서 공기와 접촉하였을 때 여러 구성성분 중에서 Mo(0)가 Mo(6+)로 산화되는 것을 확인하였는데, 아르곤이온으로 표면을 15분 정도 sputtering 하여 Mo(6+)층을 제거할 수 있었다. 합금의 구성성분 중, Mo, Ru, Rh 원소에서 내부 전자들의 결합에너지에는 커다란 변화가 없는 것으로 나타났다. 이들 화합물들의 자화율을 측정해 본 결과 2~300 K 범위에서 전형적인 Pauli-paramagnetic 행동을 보여주었다.

• 한국미생물·생명공학회지
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• 제2권2호
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• pp.83-88
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• 1974

1) 폐액을 여과했을 때 잔사부분엔 조단백질 33.08%, 총당 19.96%, 회분 2.06% 이었으며, 여액부분은 환원당 1.54%, 조단백진 2.48%, 회분이 0.43%이었으며 1kg/㎤에서 15분간 2차 살균한 결과 그의 pH가 3.15이었다. 2) 여액을 기본배지로 하여 flask 상에서 Saccharomyces cerevisiae YF-1 의 최적배양조건을 구한 결과 배지 100m1 당 Urea 0.428g, KH$_2$PO$_4$ 0.439g, MgSO$_4$ㆍ5$H_2O$ 0.21g을 첨가한 뒤 pH 4.0, 3$0^{\circ}C$ 에서 24~28시간 배양함이 가장 좋았다. 이때 배지 100m1당 1.38g의 건조효모균체 (35$^{\circ}C$에서 24시간 진공건조)를 얻을 수 있었다. 3) 건조효모의 조성은 조단백질 56.96%, 지방 1.30%, 탄수화물6.53%. 회분 9.62%이었다. 본 연구는 문교부 학술연구조성비로 행한 것이다.

• 한국식품과학회지
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• 제41권3호
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• pp.345-349
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• 2009

더덕의 육질과 껍질의 부위별 세포벽 물질(CWM)로부터 uronic acid, 총 당, 비섬유성 중성당, 페놀성 화합물 함량 및 항산화 활성을 측정하였다. 더덕의 육질과 껍질의 uronic acid와 중성당의 비는 4, 6이었다. 총 당 함량은 육질과 껍질에서 각각 788.6, 824.9 ${mu}g/g$ CWM이었다. 주요 비섬유성 중성당은 galactose와 arabinose였다. 더덕 CWM으로부터 분석된 주요 페놀성 화합물은 vanillic acid, p-OH-benzaldehyde, vanillin, ferulic acid 및 8-O-4' diferulic acid 였다. 이들 중 p-OH-benzaldehyde, vanillin, 8-O-4' diferulic acid는 더덕에서 처음으로 동정된 것으로 인삼의 세포벽 페놀성 화합물 조성과 유사하였다. 더덕의 껍질 AIR에 함유된 8-O-4' diferulic acid의 함량은 56.1 ${mu}g/g$ CWM이었다. 더덕의 CWM로부터 얻은 ethanol 분획, ethanol 분획의 ethanol-NaOH 분획, ethanol 분획 후 잔사로부터 얻은 AIR 분획의 항산화 활성의 크기는 ethanol-NaOH 분획이 가장 높았으며, 다음으로 AIR 분획, ethanol 분획의 순으로 나타났다.

• 약학회지
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• 제11권1_2호
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• pp.7-16
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• 1967

A yellowish microneedles, $C_{28}$ H$_{32}$ $O_{14}$ ${\cdot}$ I$_{1}$/$_2$, H$_{2}$O, m.p.262-$4^{\circ}$ , [${\alpha}$$_{D}^{20}$= -71,$43^{\circ}$(C = 0.42, pyridine), its acetate m.p.123-5.deg., were obtained in 0.3% yield from the leaves of Chrysanthemum sibiricum F$_{ISCHER}$. This substance is insoluble in water and the usual organic solvents except pyridine and ethylene glycol and, is not decomposed by dilute mineral acids but undergoes decomposition on being boiled in 60% H$_{2}$SO$_{4}$ or 35% HCl, giving one moel each of acacetin, glucose and rhamnose. It was not hydrolysed with a rhamnodiastase preparation obtained from the seeds of Rhamnus koraiensis. After permethylation of it, the uncrystallized product was hydrolysed and apigenin-5,4'-dimethyl ehter, m.p.$262^{\circ}$ was obtained, indicating that the disaccharide residue is at the 7 position of acacetin. Partial hydrolysis of this acacetin-7-rhamnoglucoside in cyclohexanol with formic acid gave acacetin-7-glucoside, m.p.246.deg. and rutinose, identifying them with authentic specimen on a paper chromatography. It was thus identified as linarin(acacetin-7-rutinoside) by means of mixed fusion, of paper partition chromatography and of its derivatives. Zemplen and Bognar suggested that the glucosidic linkage of linarin is .betha. by means of synthesis of this substance. But there is no evidence whether it is hydrolysed by emulsin or maltase or not. Linarin itself was not hydrolysed by an emulsin existing in the seed of Apricot or a maltase, but acacetin-7-glucoside(tilianin) which obtained from linarin gave acacetin and glucose on hydrolysis with the same emulsin and accordingly the glucosidic linkages of linarin and tilianin are thus regarded as ${\beta}$.