• 한국환경보건학회지
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• 제33권3호
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• pp.190-194
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• 2007

Aflatoxin $B_1$ is a mycotoxin produced by Aspergillus flavus and A. parasiticus and is a human carcinogen. This study was performed to investigate reduction of growth and aflatoxin production of A. parasiticus by kimchi. A. parasiticus was grown in a modified APT broth with the juice of kimchi (at a concentration of 7%) at $28^{\circ}C$ for 9 days. Aflatoxin $B_1$ was determined by use of high performance liquid chromatography (HPLC). The addition of the juice of kimchi significantly reduced mycelial growth and aflatoxin production during the incubation period (p<0.05). Reduction of mycelial growth of A. parasiticus as the result of addition of the juice of kimchi was observed to range between 64.8 to 83.4% while reduction of aflatoxin production ranged from 62.2 to 73.0%. This study indicates that kimchi could be an effective inhibitor of aflatoxin production although mycelial growth may be permitted. More research is needed to study the inhibitory effects of the metabolites of kimchi.

• Journal of Microbiology and Biotechnology
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• 제13권4호
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• pp.529-536
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• 2003

The growth-inhibitory activity of Cassia tora seed-derived materials against seven intestinal bacteria was examined in vitro, and compared with that of anthraquinone, anthraflavine, anthrarufin, and 1-hydroxyanthraquinone. The active constituent of C. tore seeds was characterized as quinizarin, using various spectroscopic analyses. The growth responses varied depending on the compound, dose, and bacterial strain tested. At 1 mg/disk, quinizarin exhibited a strong inhibition of Clostridium perfringens and moderate inhibition of Staphylococcus aureus without any adverse effects on the growth of Bifidobacterium adolescentis, B. bifidum, B. longum, and Lactobacillus casei. Furthermore, the isolate at 0.1 mg/disk showed moderate and no activity against C. perfringens and S. aureus. The structure-activity relationship revealed that anthrarufin, anthraflavine, and quinizarin moderately inhibited the growth of S. aureus. However. anthraquinone and 1-hydroxyanthraquinone did not inhibit the human intestinal bacteria tested. As for the morphological effect of 1 mg/disk quinizarin, most strains of C. perfringens were damaged and disappeared, indicating that the strong activity of quinizarin was morphologically exhibited against C. perfringens. The inhibitory effect on aflatoxin $B_1$ biotransformation by anthraquinones revealed that anthrarufin ($IC_50,\;11.49\mu\textrm{M}$) anthraflavine ($IC_50,\;26.94\mu\textrm{M}$), and quinizarin ($IC_50,\;4.12\mu\textrm{M}$), were potent inhibitors of aflatoxin ${B_1}-8,9-epoxide$ formation. However, anthraquinone and 1-hydroxyanthraquinone did not inhibit the mouse liver microsomal sample to convert aflatoxin $B_1$ to aflatoxin ${B_1}-8,9-epoxide$. These results indicate that the two hydroxyl groups on A ring of anthraquinones may be essential for inhibiting the formation of aflatoxin ${B_1}-8,9-epoxide$. Accordingly, as naturally occurring inhibitory agents, the C. tora seed-derived materials described could be useful as a preventive agent against diseases caused by harmful intestinal bacteria, such as clostridia, and as an inhibitory agent for the mouse liver microsomal conversion of aflatoxin $B_1$ to aflatoxin ${B_1}-8,9-epoxide$.

• Applied Biological Chemistry
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• 제17권2호
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• pp.143-148
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• 1974

Aflatoxin $B_1$은 전자수용성(電子受容性)을 높여주는 염화아연(鹽化亞鉛) 존재하(存在下)에서 전자공여성분자(電子供與性分子)인 Benzene과 Charge-transfer Complex를 만들며, 그 생성기구(生成機構)는 Aflatoxin $B_1$이 염화아연(鹽化亞鉛)과 일차적(一次的)으로 배위결합(配位結合)된 화합물(化合物)을 거쳐, 이것이 Benzene과 결합(結合)하여 착물(錯物)을 형성(形成)한다. 이 착물(錯物)의 안정도상수(安定度常數) 즉(卽) 평형상수(平衡常數) 0.198 l/mole이었다. 따라서 Aflatoxin $B_1$은 약(弱)한 전자수용체(電子受容體)이나, Benzene 보다 강(强)한 전자공여체(電子供與體)와는 염화아연(鹽化亞鉛)이 존재(存在)하지 않아도 Charge-transfer Complex를 만들 수 있다는 가능성(可能性)을 제시(提示)해 주는 것이며, Tryptophane, Histidine과 같은 강(强)한 전자공여체(電子供與體)를 함유(含有)한 단백질(蛋白質) 또는 Guanine, Adenine과 같은 전자공여체(電子供與體)를 함유(含有)한 DNA등(等)과의 Aflatoxin $B_1$의 결합(結合)은 그 결합(結合) Mechanism으로서 Charge-transfer Complex 형성(形成)으로 이루어진다는 추정(推定)을 할 수 있다.

• 한국환경과학회지
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• 제19권2호
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• pp.209-215
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• 2010

This study is an endeavor to evaluate the risk assessment of hazardous(aflatoxin $B_1$) in medicines from oriental medical prescription which are circulated much recently. For that, twelve globular and granule types, seven liquid types of herbal medicine were bought to compare and analyze the content of aflatoxin aflatoxin B_1), which are harmful to human body. Woo Hwang Cheong Sim Hwan of Aflatoxin $B_1$ concentration lower than the standard accepted by all the products have been detected, B company(tradition) is the concentration of $1.24\;{\mu}g/kg$, C company $1.04\;{\mu}g/kg$, A company(tradition) and B company did not detect. And the general pill of aflatoxin B1 concentration lower than the standard accepted by all the products have been detected, S-1 is the concentration of $1.8\;{\mu}g/kg$, S-2 of $1.04\;{\mu}g/kg$, S-3 of $0.88\;{\mu}g/kg$, S-4 of $9.32\l\;{\mu}g/kg$, S-6 of $7.8\;{\mu}g/kg$, S-5 did not detect. All the products eundan allowed in the concentration of aflatoxin $B_1$ levels were lower than detection, D company of $0.96\;{\mu}g/kg$, E company concentration was not detected. The liquid product of aflatoxin $B_1$ concentration was found liwer than the standard accepted by all the product, L-3 concentration of $0.8\;{\mu}g/kg$, K-4 was detected in the $1.16\;{\mu}g/kg$, L-1 and L-2 is not detected, L-5 concentration of $15\;{\mu}g/kg$, L-7 is detected as $1.08\;{\mu}g/kg$ and, L-6 was not detected.

• 한국약용작물학회지
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• 제18권5호
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• pp.338-344
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• 2010

Our paper shows the results of 302 samples of herb medicines about fungal contamination at Yakyeang markets in Seoul. The sample medicines were treated VICAM pretreatment and analysed by post column derivatisation procedure(PHRED-HPLC) with a fluorescence detector. Aflatoxin B1 was founded from 50.3% of samples, aflatoxin B2 was 39.7%, aflatoxin G1 was 21.2% and aflatoxin G2 was 23.5%. The detected ranges of aflatoxin B1, B2, G1 and G2 were from 0.1 to $57.2\;{\mu}g/kg$, 0.1 to $42.6\;{\mu}g/kg$, 0.1 to $23.5\;{\mu}g/kg$ and 0.1 to $9.5\;{\mu}g/kg$ respectively. Among total samples, 26 samples contained aflatoxin B1 violated the regulation (less than 10 ug/kg) for aflatoxin B1 of KFDA. From the result, we could presumed that more than a half of samples were contaminated by aflatoxins. Therefore, it seems to be necessary that the new safety giudeline will be established aflatoxin B2, G1 and G2 from herb medicines as aflatoxin B1.

• 한국식품위생안전성학회지
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• 제13권3호
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• pp.313-317
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• 1998

본 연구는 한국 전통 된장과 간장 및 메주등에서 주된 상재균으로 나타나는 B. subtilli가 Aspergillus parasicus의 성장과 발암물질(Aflatoxin) 생성에 미치는 영향을 관찰하기 위하여 수행되었다 변형 APT 배지를 사용하여 $30^{\circ}C$에서 12일 동안 B. subtilis KCCM 11316과 Aspergillu parasiticus ATCC 15517를 단독 배양(대조군) 및 혼합 배양하고 그 성장과 배양물의 변화를 경시적으로 관찰하였으며 HPLC에 의하여 aflatoxin을 분석하였다. 혼합 배양시에는 곰팡이의 건조 균체량이 배양 직후로부터 배양 말기에 이르기까지 현저하게 억제되었으며, 배양 말기에 단독 배양시보다 85.3% 감소되었다(p<0.01). Aflatoxin의 생성량도 배양 말기에 대조군에 비하여 50%이상 감소되었다(p<0.05). 이로부터 Bacillus subtilis는 메주 및 간장과 된장에 있어서 유해 곰팡이의 생육과 aflatoxin 생성을 주도적으로 억제하는 것을 알 수 있다. Aflatoxin 생성에 대한 억제 효과는 곰팡이의 성장에 대한 억제 효과보다 낮게 나타났으나 메주 중에는 다른 발효 관련 세균들이 함께 존재하는 바, 이들에 의한 억제적 영향도 기대된다.

• 한국식품위생안전성학회지
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• 제31권1호
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• pp.36-41
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• 2016

Ochratoxin A와 aflatoxin은 곰팡이 독소 생산 균주가 자연 발효되는 식품에 오염되거나 발표식품의 종균을 분별없이 선택했을 때 검출 될 수 있다. 본 연구에서는 다양한 배양 환경이 ochratoxin A와 aflatoxin의 생산에 주는 영향에 대해 연구하였다. Aspergillus usamii KFRI 999와 A. awamori KFRI 983의 배양 온도, 배양 배지, 배양 시간을 달리하여 ochratoxin A생산 정도를 분석하였다. 또한 초기 pH, 온도, 배양 시간, 배양 배지를 다르게 하였을 때 A. flavus KACC 41403와 A. oryzae KACC 46471가 생산하는 aflatoxin의 양을 평가하였다. Ochratoxin A와 aflatoxin의 양은 HPLC로 분석하였다. 연구 결과, 곰팡이 독소는 배양 온도에 큰 영향을 받는 것으로 나타났다. A. oryzae KACC 46471는 aflatoxin을 생산하지 않았다. 곰팡이 독소를 생산하는 균주는 모두 $30^{\circ}C$에서 가장 높은 독소 생산량을 보였다. A. awamori KFRI 983은 PDA 배지에서 가장 적은 ochratoxin A 생산량을 보였다. 본 연구 결과는 다양한 식품의 ochratoxin A와 aflatoxin 저감화에 유용하게 활용 될 수 있다.

• Journal of Dairy Science and Biotechnology
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• 제37권1호
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• pp.1-14
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• 2019

일반적으로 우유는 필요한 영양분이 풍부한 식품으로 사람의 건강 증진, 유지 등에 큰 도움을 주고 있다. 하지만 전 세계적으로 우유와 유제품에 Aflatoxin M1의 존재는 20~30년 전부터 알려져 왔다. Aflatoxin M1으로 오염된 우유와 유제품은 특히 지난 10년에서 20년 동안 전 세계적으로 중요한 문제이다. 특히, 이 제품들에서의 미코톡신의 존재는 특히 성인보다 더 민감한 어린이와 유아에게 중요한 문제이다. 이 총설에서는 최근의 자료를 검토하여 전 세계적으로 다양한 지역에서 생산되는 우유 및 유제품에서 발생한 Aflatoxin M1의 현황, 관련 규정, 감소 전략, 검출 방법, 향후 연구과제 등을 정리하였다. 우유 및 유제품의 Aflatoxin M1 오염을 최소화하기 위해서는 지속적으로 발전하고 있는 분석 기법을 이용한 엄격한 규제와 우수한 우유 처리기술이 반드시 필요하다. 더 나아가서, 우유 및 유제품에 존재할 수 있는 Aflatoxin M1이 인체 건강의 미치는 영향을 올바른 인식할 수 있도록 교육도 함께 진행되어야 할 것이다.

• 한국식품위생안전성학회지
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• 제1권1호
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• pp.23-29
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• 1986

In this study, th effective extraction of 5 vegetables, which have been shown to inhibit the growth of the aflatoxin production of Aspergillus parasiticus R-716, was investigated and their effects were examined. Radish, cabbage, garlic and zinger were effectively with water-chloroform, but crown daisy with n-hexane. Among them, water-chloroform extract of radish was remarkably effective, and garlic extract only inhibited the growth strongly. The growth and the aflatoxin production of the strain were showed 0.758g/25ml, 763ug/25ml with the addition of water-chloroform extract equivalent 15g of raw radish, and an increase in the level of radish extract resulted in a decrease both the growth and the aflatoxin production per mycerial weight.

• 한국환경보건학회지
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• 제20권4호
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• pp.90-97
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• 1994

This study was performed to investigate the effect of the Panax ginseng C. A. Meyer on the growth and production of aflatoxin by Aspergillus flayus ATCC 15517. Asp. fiavus with 10$^6$ conidia was incubated at 30$\circ$C for 7 days on YES broth containing 0.1%, 0.5%, and 1.0% of ginseng extract. After incubation, dry mycelial weight, pH, and production of aflatoxin were investigated. The results were as follows:There was no significant difference in dry mycelial weight by the addition of 0.1% and 0.5% ginseng extract. However, it was decreased to the rate of 13.7% by the addition of 1.0% ginseng extract in 7 days. pH changes in cultures were similar regardless of the concentration of ginseng extract. The pH values decreased to minimum in 5 days and again increased. Aflatoxin production was reduced as the concentration of ginseng extract increased. When compared to the control, the production of total aflatoxin significantly reduced to 56.7%, 54.0%, 53.3% in the media of 0.1%, 0.5% and 1.0% of ginseng extract, respectively. No significant difference was observed among ginseng extract groups.