• 설비공학논문집
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• 제8권4호
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• pp.473-483
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• 1996

To protect the ozone layer, R22 will be replaced with HFCs. R407C is a leading candidate as alternative refrigerant for air conditioner due to its similar thermodynamic characteristics with R22. In replacing R22 with R407C, the compatibility with lubricating oil is of major concern. Polyol ester (POE) oil among the synthetic oils is considered to be the best lubricant for use with R407C because of good electrical properties and miscibility. However, lubricating ability of mixture of R407C/POE oil is lower than that of R22/mineral oil due to the production of acid by hydrolysis which causes corrosive wear. Therefore, to minimize water content, it is needed to develop a molecular sieve desiccant which is compatible with R407C and ester oil. This paper discusses (1) the change of properties of POE oil when current molecular seive is used, (2) the effects of POE oils and additives on durability of compressor. Through compressor life test and bench wear test, it was found that inadequate use of POE oils and additives may promote the deteriation of molecular sieve, resulting in decrease of durability of compressor.

• 한국식품과학회지
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• 제25권1호
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• pp.9-14
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• 1993

탈지들깨박으로부터 추출한 유리페놀산, 페놀산 에스터 및 불용성 결합형 페놀산 형태의 페놀화합물들의 항산화효과를 일반 시판용 합성항산화제들과 비교하였다. Chlorogenic acid를 표준물로써 비색법으로 측정한 페놀화합물들의 총함량은 0.75%였고 총페놀산중 유리페놀산, 페놀산 에스터 및 불용성 페놀산 추출물이 차지하는 비율은 각각 87.5, 7.5, 5.0%였다. 이차원 전개법에 의한 paper chromatography 성분분석 결과 유리페놀산 형태의 추출물에서는 대부분의 폐놀화합물이 chlorogenic acid와 일치하였고 소량의 caffeic acid와도 일치되었으나, 페놀산 에스터와 불용성 결합형 페놀산 형태의 추출물에서는 나타나지 않았다. 30g의 탈지들깨 종자박에서 추출된 각 형태의 페놀산 추출물들은 각각의 페놀함량 차이가 큼에도 불구하고 식용대두유 기질에서 0.02%(w/w) 농도로 첨가된 BHT와 비슷한 정도의 항산화 효과를 나타냈다.

• Anatomy and Cell Biology
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• 제57권1호
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• pp.97-104
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• 2024

Heavy reliance on glucose metabolism and a reduced capacity to use ketone bodies makes glioblastoma (GBM) a promising candidate for ketone-based therapies. Ketogenic diet (KD) is well-known for its promising effects in controlling tumor growth in GBM. Moreover, synthetic ketone ester (KE) has demonstrated to increase blood ketone levels and enhance animal survival in a metastatic VM-M3 murine tumor model. Here, we compared the efficacy of a KE-supplemented Atkins-type diet (ATD-KE) to a classic KD in controlling tumor progression and enhancing survival in a clinically relevant orthotopic patient-derived xenograft GBM model. Our findings demonstrate that ATD-KE preserves body weight (percent change from the baseline; 112±2.99 vs. 116.9±2.52 and 104.8±3.67), decreases blood glucose (80.55±0.86 vs. 118.6±9.51 and 52.35±3.89 mg/dl), and increases ketone bodies in blood (1.15±0.03 mM vs. 0.55±0.04 and 2.66±0.21 mM) and brain tumor tissue (3.35±0.30 mM vs. 2.04±0.3 and 4.25±0.25 mM) comparable to the KD (results presented for ATD-KE vs. standard diet [STD] and KD, respectively). Importantly, the ATD-KE treatment significantly enhanced survival compared to the STD and was indistinguishable from the KD (47 days in STD vs. 56 days in KD and ATD-KE), suggesting that a nutritionally balanced low carbohydrate ATD combined with KE may be as effective as the KD alone in reducing brain tumor progression. Overall, these data support the rationale for clinical testing of KE-supplemented low-carb diet as an adjunct treatment for brain tumor patients.

• 한국식품과학회지
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• 제27권4호
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• pp.564-570
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• 1995

Aspartame의 전구체인 BzAPM을 고정화 thermolysin으로 합성할 때 최적 조건을 찾고자 기질의 농도, 반응 pH 및 온도 그리고 금속이온, benzoic acid, Phe, NaCl의 농도가 어떤 영향을 주는지 조사하였다. 반응기질인 PheOMe와 BzAsp를 25% DMSO 및 20% PEG 200이 함유된 유기 용매계에서 반응시켰다. Bz-Asp의 농도를 100 mM로 일정하게 하였을 때 BzAPM의 합성 속도는 PheOMe의 농도가 증가함에 따라 직선형으로 증가하였으며, PheOMe의 농도를 300 mM로 하고 Bz-Asp의 농도를 변경시킨 경우에는 200 mM에서 반응 속도가 최고에 달하였다. BzAPM의 생산을 위한 최적 pH는 6.1 전후로 나타났으며, 최적 반응 온도는 $40^{\circ}C$이었다. 2가 금속 이온을 5mM로 첨가했을 때, $Zn^{2+},\;Mg^{2+},\;Fe^{2+},\;Cu^{2+}$이온은 고정화 thermolysin의 BzAPM 합성 수율을 저하시켰으나, $Co^{2+}$ 이온은 합성 수율을 2배 정도 증가시키는 것으로 확인되었다. $Co^{2+}$ 이온을 $Ca^{2+}$ 이온과 함께 첨가하면 $Co^{2+}$이온만 첨가할 때보다 합성 수율이 높게 나타났다. Benzoic acid와 Phe이 BzAPM의 합성을 저해하는 것으로 나타났으며, NaCl도 10% 농도로 첨가시에 합성을 약 25% 저하시켰다.

• Preventive Nutrition and Food Science
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• 제5권2호
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• pp.86-92
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• 2000

Conjugated linoleic acid(CLA) refers to a collective term of positional and geometric isomers of linoleic acid, which are different in their biological activities. The predominant isomer of CLA in animal tissues is cis-9, trans-11; smaller amounts of trans-10, cis-12 CLA isomers, CLA methyl ester (CLA-ME) was chemically syn-thesized from linoleic acid by the alkaline isomerization method. The synthetic CLA-ME, mainly composed of cis-9, trans-11 CLA and trans-10, cis-12 CLA, was dissolved in acetone, stored at 68$^{\circ}C$ for 1 day, and the supernatant(cis-9, trans-11 CLA-Me) was separated from the precipitate (trans-10, cis-12 CLA-Me). After the processes were repeated three times at -68$^{\circ}C$, the whole processes were repeated three times at -71$^{\circ}C$ in order to increase the purity of these two isomers. The cis-9, trans-11 CLA-Me and trans-10, cis-12 CLA isomers were further purified by the urea adduct. Purities of the cis-9, trans-11 CLA-Me and trans-10, cis-12 CLA-Me were 90.3 and 99.9%, respec-tively. This method could be employed for the preparation of a large quantity of highly purified cis-9, trans-11 CLA-Me or trans-10, cis-12 CLA-Me from synthetic CLA-Me.

• 한국식품과학회지
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• 제25권2호
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• pp.148-153
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• 1993

최근 sucrose polyesters(SPE)와 더불어 유지대체 물질로서의 사용이 검토되고 있는 glucitol fatty acid polyesters(GPE)를 합성한 후, 화학적 구조 및 상대적 에스테르 분포에 따른 치환도를 조사하였다. 본 연구에서 합성한 GPE는 순상 HPLC에 의해 단일 에스테르 그룹으로 분리되었으며, 분리된 에스테르 그룹의 치환도는 6으로서 GPE 전체가 glucitol fatty acid hexaester임을 알 수 있었다. GPE의 IR 스펙트럼에서 $1747\;cm^{-1}$에 나타나는 흡수대는 GPE 분자내에 glucitol과 지방산을 연결하고 있는 에스테르 결합이 존재함을 보여주었다. GPE는 H-NMR 스펙트럼에서는 glucitol의 hydroxyl proton의 시그널이 존재하지 않음을 볼 때 glucitol의 모든 수산기가 지방산과의 에스테르 결합에 참여하고 있음을 알 수 있었다. 또한 GPE의 H-NHR 스펙트럼을 정량적으로 해석한 결과는 수산기가(hydroxyl value) 측정에 의해 결정된 GPE의 치환도와 일치하였다. 이상의 결과를 종합하여 볼 때 본 연구에서 합성한 GPE는 glucitol fatty acid hexaester임이 확인되었고 향후 유지대체물질로서 사용되어질 가능성을 지닌 것으로 생각되었다.

• 한국윤활학회:학술대회논문집
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• 한국윤활학회 2001년도 제33회 춘계학술대회 개최
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• pp.162-177
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• 2001

분자구조가 서로 다른 7종의 폴리올에스터 오일에 대한 가수분해속도가 측정되었다. 사용된 폴리올에스터는 2가 및 4가의 다가알콜과 서로 다른 탄소수의 직쇄 흑은 분기지방산으로 합성된 다가에스터 화합물이며, 이들의 가수분해반응은 p-톨루엔설폰산을 촉매로 사용하는 온건한 산성조건하에서 수행되었다 폴리올에스터 오일의 가수분해과정에서 생성되 는 부분에스터와 다가알콜 및 지방산 등의 구조가 확인되었고 반응시간의 경과에 따른 가수분해 생성물들의 농도가 측정되었다. 각 반응단계의 속도상수는 속도식과 실험적으로 얻은 각 화합물들의 농도로부터 최소제곱법에 의해 구하였고, 얻어진 가수분해 속도상수가 서로 비교되었다. 폴리올에스터 오일의 가수분해 속도는 지방산의 분자구조에 가장 크게 영향을 받는다. 즉, 직쇄지방산에 의한 폴리올에스터 오일은 분기지방산에 의한 폴리올에스터 오일보다 가수분해속도가 매우 마르며, 분기지방산에 의한 폴리을에스터 오일 중에서는 가지사슬의 모양과 위치가 가수분해속도에 영향을 미치는 것으로 확인되었다. 본연구에서 사용된 7종의 폴리올에스터 오일에 대한 가수분해속도는 물분자가 폴리올에스터 오일의 카르보닐 탄소를 공격할 때 인접한 가지사슬에 의한 입체장애효과를 비교함으로써 효과적으로 설명할 수 있다.

• 대한수의학회지
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• 제25권1호
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• pp.7-17
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• 1985

Many investigators have been pursuing various attempts so far to produce hepatitis B surface antigen(HBsAg) vaccines using the techniques such as isolation from plasma of chronic HBsAg carrier, recombinant DNA technique or preparation of synthetic peptides specific for immunogenic determinants. Hepatitis B virus can not grow on any cell lines by the tissue culture technique at the present time. The plasma of chronic HBsAg carrier is expensive and its source is limited. The HBsAg from the recombinant DNA technique gave still very low yield. Another approach, therefore, has been initiated to develop a synthetic hepatitis B virus vaccine. The possible use of several distinct synthetic vaccines in prophylaxis can be facilitated by availability of full synthetic immunogens. Peptides synthesized for potential application as antiviral vaccines have been mostly tested in the form of conjugates with carrier proteins, although the free synthetic peptide can be immunogenic. To understand basic knowledges on the antigenicity and immunogenicity of a synthetic peptide specific for major immunogenic determinant of HBsAg, a nonapeptide, $H_2N^{139}Cys-Thr-Lys-Pro-Thr-Asp-Gly-^{146}Asn-Aba$ COOH, which corresponds to HBsAg amino acid residues 139 to 147, was synthesized by the Merrifield's solid-phase method with a slight modification. The antigenicity and immunogenicity of this specific synthetic peptide were examined comparing with purified plasma-derived natural HBsAg. The results obtained are as follows; 1. The peptide synthesized showed the identical amino acid composition to the theoretical value. The degree of purification and molecular weight were acertained by methods of high performance liquid chromatography and mass spectrometry. 2. Using m-maleimidobenzoyl-N-hydroxysuccinimide ester as a conjugating agent, the synthetic peptide was conjugated to rabbit albumin and ${\gamma}$-globulin, tetanus and diphtheria toxoids, and keyhole limpet hemocyanin. Their conjugation yields were 8.3, 9.5, 15.8, 13.5, and 11.2%, respectively. 3. The natural HBsAg was purified from plasma of chronic HBsAg carrier. By the electron microscopic observation of the purified natural HBsAg preparation, no Dane particles were observed and the preparation showed negative DNA polymerase activity. 4. Antigenicity of the synthetic peptide and the plasma-derived natural HBsAg was determined by competition radioimmunoassay using $^{125}I$-natural HBsAg. Their 50% inhibitions appeared as $90{\mu}g/ml$ and $0.12{\mu}g/ml$ for the synthetic peptide and the natural HBsAg, respectively. This indicates that the former was about 750-fold less antigenic than the latter. 5. Immunogenicity of the synthetic peptide was determined by administering the peptide-carrier conjugates into rabbits with and without Freund's complete adjuvant. Regardless the carrier proteins and adjuvant, positive immune responses to the synthetic peptide were observed. The higher antibody titers, however, were shown in the groups administered with Freund's complete adjuvant. 6. Immunizing dose 50% in mice of the various peptide-carrier conjugates was 5.47, 6.00, 65.16, 31.25 and $13.03{\mu}g/dose$ for rabbit albumin and ${\gamma}$-globulin, tetanus and diphtheria toxoids, and keyhole limpet hemocyanin, respectively, while the natural HBsAg showed $0.65{\mu}g/dose$. 7. It was postulated that homologous proteins prefer to heterologous ones as the carriers.

• Journal of Photoscience
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• 제9권2호
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• pp.353-355
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• 2002

We prepared 3-(1-hydroxyethyl)-bacteriopyrochlorophy11-a (3) possessing magnesium atom and phytyl ester from modification of natural bacteriochlorophyll(BChl)-a. A dichloromethane solution of (3$^1$R) and (3$^1$S)-3 was diluted with 100~1000 fold volume of cyclohexane to give new species absorbing near-infrared lights. The resulting Q, maximum of (3$^1$R)-3 was 860 nm and red-shifted by 2150 $cm^{-1}$ / from the monomeric. In the nonpolar organic solvent, epimeric (3$^1$S)-3 showed a 1ess red-shifted peak at 798 nm as well as a residual monomeric band. Such visible spectra indicated that 3 diastereose1ectively aggregated in cyclohexane to afford oligomers possessing a simi1ar supramolecular structure with chlorosomal aggregates of natural BChl-d, 7,8-dehydro-form of 3.

• Journal of Microbiology and Biotechnology
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• 제7권5호
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• pp.333-340
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• 1997

An actinomycetes, KT-10 isolated from ginseng field in Kyongpook, Korea was selected based on its ability to produce a lysosomal cathepsin B inhibitor. The inhibitor purified from the culture supernatant of the isolate KT-10 showed strong inhibitory effects against cathepsin B as well as against papain when the activities were measured using synthetic substrate, ${\alpha}$-N-benzyloxycarbonyl-L-Iysine p-nitrophenyl ester (CLN) or ${\alpha}$-N-benzoyl-D,L-arginine 2-naphthylamide (BANA). The isolate KT-10 was identified as a species of Streptomyces based on its morphological characteristics and chemotaxonomic data. The TAXON program of Ward was used to identify Streptomyces sp. KT-10 as a strain of Streptomyces luteogriseus belong to cluster 18 of the genus Streptomyces with a Willcox probability 0.999388. The cathepsin B inhibitor was presumed to a novel material composed of a polyhydroxylamine.