• 한국식품위생안전성학회지
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• 제10권1호
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• pp.1-6
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• 1995

In order to establish the enzyme linked immunosorbent assay(ELISA) of sterigmatocystin produced by Aspergillus versicolor, we experimented and obtained following results. Two of three rabbits which had been immunized with sterigmatocystin-hemiacetal-BSA produced antibodies against sterigmatocystin at 15 weeks. The produced antibodies were specific for sterigmatocystin and sterigmatocystin-hemiacetal but didn't cross react with other sterigmatocystin analogues in a significant degree. DMF : 4% KC1 (18 : 2) mixed solution was most effective to dissolve sterigmatocystin. For the preparation of sample solution to determine sterigmatocystin by ELISA, sample was extracted with CHC13 and dried, than the dried sample was redissolved with 100 ${mu}ell$ DMF + 4% KC1 mixture. 10~1,000 ng/$m\ell$ level of standard sterigmatocystin could be applied to the established ELISA. When artifically contaminated rice were assayed by the ELISA, the average recovery of sterigmatocystin spiked to 25~500 ng/g was 109% (97~116%), and mean interwell coefficient of variation was 21% (11~28%).

• 한국산학기술학회:학술대회논문집
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• 한국산학기술학회 2011년도 춘계학술논문집 1부
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• pp.141-143
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• 2011

Al-SBA-1(Si/Al = 40, 80 and 120) and Al,Mg-SBA-1 (Si/(Al+Mg) = 40 and 80) molecular sieves were synthesized and characterized. Acetalization of n-heptanal with methanol was studied under autogenous pressure between 80 and $150^{\circ}C$. Since protonation of n-heptanal was fast, addition of methanol to the same to formed hemiacetal slowly whereas conversion of hemiacetal to acetal was fast. The catalysts exhibited nearly similar conversion irrespective of their difference in acidity, and all of them showed more than 80 % conversion either at 80 or $100^{\circ}C$. Hence it is evident that the difference in acidity is not so important in differentiating the activity of the catalysts. The large pore size and hydrophilic and hydrophobic properties are suggested to be the main factors that control acetalization.

• Bulletin of the Korean Chemical Society
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• 제35권12호
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• pp.3423-3424
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• 2014

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1994년도 춘계학술대회 and 제3회 신약개발 연구발표회
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• pp.222-222
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• 1994

목적하는 화합물인 2',5'-dihydroxy-3'-무치환 유도체(1)는 uridine을 sodium metaperiodate로 산화하여 dialdehyde를 얻은다음 1,2-dianilinoethane으로 3'-aldehyde만을 선택적으로 보호, 2'-aldehyde를 NaBH$_4$로 환원, alcohol로 하여 deprotection 하므로서 hemiacetal율 얻는다. 이 hemiacetal을 TsSNHHNH$_2$로 처리하여 목적하는(1) 화합물을 얻었으며 2-azido-5-Hydroxy-3'-무치환 유도체(2)는 (1)화합물 합성시 얻은 hemiactal을 출발 물질로 하여 먼저 TBDPSCl로 silyaltion하여 5'-hydroxyl group을 보호하고 TsNHNH$_2$로 3'-위치를 hydrazone으로 한다음 NaB(CNH$_3$로 처리하여 얻은 hydrazide를 NaOAc를 반응시켜 2'-hydroxy-3'-무치환-5'-silyl 유도체를 얻고 또한 2',3'-dihydroxy group을 tosyl화, azido화, 5'-silyl group을 deprotection 하므로서 (2)를 얻었다. 또한 2',3'-dihydroxy-5'-무치환 유도체(4)는 uridine의 2',3'-위치를 먼저 protection, 5'-위치를 benzoyl화 2',3'-deprotection, periodate oxidation하여 얻은 diol을 silyl화 한 다음 5'-위치를 benzoyl화, 2',3'-deprotection, 산화하여 얻은 hemiacetal의 silyl group을 제거한후 primary hydroxyl group만을 선택적으로 silyl화, TsNHNH$_2$, NaB(CN)H$_3$ 및 NaOAc로 처리하므로서 얻은 2'-hydroxy-3'-0-silyl group-5'-무치환 화합물을 tosyl, azido화 한다음 desilylation하여 얻었다. 목적하는(1) 화합물의 diasteromer 인 2',3'-dihydroxy-5'-무치환 유도체(3)는 (4)화합물 합성시 얻은 hemiactal을 key intermediate로 하여 TsNHNH$_2$, NaB(CN)H$_3$ 및 NaOAc로 처리하므로서 얻을수 있었다. 이들 화합물들의 각종 DNA 및 RNA virus에 대한 항 바이러스작용을 검토한 결과 현저한 항 바이러스 작용을 나타내지 않았다.

• 한국식품위생안전성학회지
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• 제7권1호
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• pp.15-22
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• 1992

농산물 및 그 가공식품을 수확·저장·가공하는 기간중에 Aspergillus parasiticus가 오염되어 aflatoxin을 생성하는 것을 방지할 목적으로 생육배지에 graefruit 종자추출물(GFSE)을 처리하여 곰팡이의 생육 및 aflatoxin 생합성을 저해하는 뚜렷한 효과를 관찰할 수 있었다. 4000 ppm의 GFSE농도 처리로 Aspergillus parasiticus의 생육을 92% 저해하였으며, 5000ppm 농도에서는 곰팡이 생육을 완전히 저해하였고 3000ppm 이상의 농도에서 aflatoxin 의생성을 100% 억제하였다. 한편, GFSE 처리에 의하여 aflatoxin 생합성 경로증, averufin, versiconal acetate 등의 중간대사산물이 aflatoxin으로 주입되는 것이 완전히 저해된 반면, versicolorin A, versicolorin A hemiacetal, sterigmatocystin 등은 aflatoxin 으로 전환되는 결과를 보여주어 GFSE는 versiconal acetate를 포함한 그 이전의 중간 대사물이 반응기질이 되는 효소 반응계를 저해하는 것으로 나타났다. 전자현미경을 이용한 곰팡이균체 및 포자의 형태변화는 GFSE처리에 의하여 세포막기능에 파괴되어 세포구성 내용물이 유실되고 곰팡이가 사멸하고 aflatoxin 생합성 기작이 중단되는 결과를 초래하였다.

• Journal of Microbiology and Biotechnology
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• 제25권6호
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• pp.814-819
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• 2015

The natural crosslinking agent genipin has been applied widely in biomedicines and foods nowadays. Because of the special hemiacetal ring structure in its molecule, it can only be prepared by hydrolysis of geniposide according to biocatalysis. In this research, strategies including aqueous-organic biphasic catalysis and substrate fed-batch mode were adopted to improve the biocatalysis process of genipin. A 10 L ethyl acetate-aqueous biphasic system with geniposide fed-batch led to a satisfying genipin yield. With Fusarium solani ACCC 36223, 15.7 g/l genipin in the ethyl acetate phase was obtained, corresponding to space-time yields of 0.654 g l^-1 h^-1.

• 한국식품과학회지
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• 제44권2호
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• pp.247-250
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• 2012

본 연구에서 적용한 시험법의 회수율은 97.4-122.5%, 상대표준편차(RSD)는 6%이내로서 적합한 시험법임을 확인하였다. 조사된 원유 및 시유의 검출농도는 아플라톡신 $M_1$이 평균 29.6 ng/kg(5.4-72.7 ng/kg)로 나타났으며, 원유 및 시유에 대한 아플라톡신 $M_1$ 오염수준은 현행 식품공전에서 정한 허용기준치인 500 ng/kg 보다 낮은 안전한 수준인 것으로 판단된다.

• 대한약침학회지
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• 제3권2호
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• pp.1-25
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• 2000

We were trying to study the validity of Puffer fish's poison(Tetrodotoxin- TTX) to make a traditional Korean Medical treatment. The following conclusions were made after literary studies. 1. The first record of the puffer fish dates back 2000 years ago in the Chinese text Book of Mountain and Sea and other texts from the similar period. 2. Puffer fish's poison IS known as tetrodotoxin which is an amino perhydroquinazoline compound. It has a chemical formula of $C_{11}H_{17}N_3O_8$ in the hemiacetal structure and has the molecular weight of 319. 3. Tetrodotoxin (TTX) plays a role as potent neurotransmitter blocker by blocking the $Na^+$ -gate channel which hinders the influx of $Na^+$ ion into the cell. 4. Symptoms of the puffer fish poisoning ranges from blunted sense in the lips and tongue, occasional vomiting in the first degree to sudden descending of the blood pressure, apnea, and other critical conditions in the fourth degree. Intoxication of the puffer fish poison progresses at a rapid pace as death may occur after an hour and half up to eight hours in maximum. Typical death occurs after four to six hours. 5. Ways to treat the puffer fish poisoning include gastric irrigation, induce vomiting, purgation, intravenous fluid injection, and correcting electrolytic imbalance and acidosis. In cases of dyspnea, apply oxygen inhalation and conduct artificial respiration. 6. Tetrodotoxin (TTX) may be applied in treating brain disorders, ocular pain, excess pain in the large intestine and ileum, and relieving tension of the skeletal museles, neuralgia, rheumatism, arthritis, and etc. 7. In terms of Oriental medicine, the puffer fish poison has characteristics of sweet, warm, and poisonous. It's known efficacies are to tonify weakness, dispel damp, benefit the lower back, relieve hemorrhoid, kills parasites, remove edema, and so forth. And the puffer fish eggs processed with ginger are said to be effective against tuberculosis and lung cancer, thus, it's validity must be investigated and further research should be followed.