• 한국식품조리과학회지
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• 제11권1호
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• pp.77-82
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• 1995

Boiled, broiled, deep fried, pan fried 등의 방법으로 조리된 조기와 돼지고기의 50% methanol 추출물에 S9 mix를 첨가한 군, S9 mix를 첨가하지 않은 군, 그리고 nitrite를 처리한 군을 Salmonella typhimurium TA98과 TA100으로 Ames test를 실시하여 돌연변이원 형성을 검토한 결과는 다음과 같다. 1. S9 mix를 첨가하지 않은 조기와 돼지고기는 original weight 0.0125 g과 0.1 g사이의 농도 구간에서 돌연변이 원성을 보였다. 2. S9 mix 첨가시 조기와 돼지고기의 돌연변이원성은 모든 농도 구간에서 S9 mix를 첨가하지 않은 경우보다 2∼5배 정도 증가하여 간접 돌연변이원이 존재함을 확인하였다. 3. TA98과 TA100에 대한 돌연변이원성은 모든 조리법에서 조기보다 돼지고기가 더 높았고, 특히 pan fried법의 경우 S9 mix의 첨가시 돌연변이원성이 매우 높게 나타났다. 4. 조기와 돼지고기의 모든 조리법에서 nitrite 처리시 TA98과 TA100 모두 돌연변이원성이 증가하여 직접돌연변이원임을 나타냈고, 특히 TA100보다 TA98에서 돌연변이원성이 더 높은 것으로 나타났다.

• 한국식품과학회지
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• 제31권3호
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• pp.823-830
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• 1999

배양 CHO cell에 SCE법을 이용하여 실제로 음용하는 조건에서 추출한 시판 감잎차, 녹차, 우롱차 추출물의 돌연변이 억제효과를 보기 위하여 실험하였다. 돌연변이 물질로 사용한 MMC에 의하여 유발된 SCE 빈도에 미치는 각 차 추출물의 돌연변이 억제 효과를 본 결과, 감잎차는 MMC 처리 후 S9 mix와 함께 고농도$(1000\;{\mu}g/mL)$로 세포에 처리되었을 때 SCE 빈도를 유의하게 감소시켰다. S9 mix 없이 감잎차 추출물만을 후처리한 경우는 저농도$(20{\sim}80\;{\mu}g/mL)$에서 SCE 유발빈도를 유의하게 감소시켰다. 우롱차는 MMC처리 후 S9 mix와 함께 저농도$(10{\sim}20\;{\mu}g/mL)$로 처리 시 SCE 유발빈도를 감소시키는 효과가 있었으며, 녹차는 MMC 처리 후 S9 mix와 함께 추출물 농도 $160\;{\mu}g/mL$로 처리 시 SCE 유발빈도를 감소시키는 효과가 있었다. 감잎차, 녹차, 우롱차 모두 농도는 다르나 각 추출물을 S9 mix와 함께 세포분열 주기 중 G1기에 후 처리 되었을 때에 SCE 빈도를 감소시키는 효과가 있었으며, 감잎차는 S9 mix 없이 단독으로 후처리 되었을 때에도 용량 상관성은 없지만 SCE 빈도를 감소시키는 효과가 있었다. 결론적으로, 시판 감잎차, 녹차, 우롱차 추출물에는 MMC로 유발된 돌연변이를 억제시키는 효과가 있는 것을 확인할 수 있었으며, 감잎차의 경우 S9 mix 없이도 SCE 빈도를 감소시키는 효과가 있었던 것으로 보아 다른 두 차와는 다른 기전의 돌연변이 억제 작용을 하는 성분이 있는 것으로 사료된다.

• Molecular & Cellular Toxicology
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• 제3권1호
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• pp.53-59
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• 2007

This study was conducted to evaluate the mutagenic potential of dimethyl isophthalate (DMIP) using Ames bacterial reverse mutation test, chromosomal aberration test and mouse lymphoma $tk^{+/-}$ gene assay. As results, in Ames bacterial reversion assay, DMIP was tested up to the concentration of 5,000 ${\mu}g$/plate and did not induce mutagenicity in Salmonella typhimurium strains TA98, TA100, TA1535 and TA1537, and Escherichia coli WP2uvrA with or without metabolic activation (S9 mix). Using cytotoxicity test, the maximal doses of DMIP for chromosomal aberration assay were determined at 1,250 ${\mu}g/mL$, which was a minimum precipitation concentration ($IC_{50}>1,940\;{\mu}g/mL$ or 10 mM) and at 155 ${\mu}g/mL$ ($IC_{50}:155\;{\mu}g/mL$) in the presence and the absence, respectively, of S9 mix. DMIP in the presence of S9 mix induced statistically significant (P<0.001) increases in the number of cells with chromosome aberrations at the dose levels of over 250 ${\mu}g/mL$, when compared with the negative control. However, DMIP in the absence of S9 mix did not caused significant induction in chromosomal aberrant cells. In MLA, DMIP at the dose range of 242.5-1,940 ${\mu}g/mL$ in the presence of S9 mix induced statistically significant increases in mutation frequencies related to small colony growth, whereas any significant mutation frequency was not observed in absence of S9 mix. From these results, it is conclusively suggested that dimethyl isophthalate may be a clastogen rather than a point mutagen.

• 한국식품영양과학회지
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• 제36권8호
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• pp.960-964
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• 2007

천연생리활성물질 소재로서 파고지 추출물의 안전성을 검증하기 위하여 렛트에 대한 단회 경구투여 독성 평가와 복귀돌연변이평가를 실시하였다. 파고지 에탄올 추출분말 2 g/kg, 5 mL를 암${\cdot}$수 각각 5마리씩 경구 투여한 후 14일 동안의 일반증상, 체중변화 및 부검시의 육안적 소견을 관찰한 결과, 사망례, 일반증상 및 체중변화는 관찰되지 않았고 부검결과에서도 특이할 만한 육안적 이상소견은 관찰되지 않아, 파고지 추출물은 $LD_{50}$값이 렛트 체중 kg당 2g 이상이며 단회 경구 투여에 대한 독성을 가지는 않는 것으로 평가되었다. 파고지 추출분말의 복귀돌연변이 유발성 여부는, 히스티딘 요구성 Salmonella Typhimurium TA98, TA100, TA1535, TA1537 균주 및 트립토판 요구성 Escherichia coli WP2uvrA(pKM101) 균주를 이용하여 S9 mix 첨가 여부에 따라 실험하였다. 용량설정시험 결과, S9 mix 첨가 여부에 관계없이 사용한 모든 시험균주에서 생육저해가 관찰되었다. 시험물질의 석출은 S9 mix 첨가 여부와 상관없이 사용한 모든 시험균주의 1,250, 2,500 및 5,000 ${\mu}g/plate$에서 관찰되었지만 콜로니 계수에는 영향이 없었다. 따라서, 본 시험의　용량은 S9 mix 미첨가 TA100, TA1537 균주 및 S9 mix 첨가 RA1535 균주의 경우에는 생육저해가 관찰된 625 ${\mu}g/plate$를, S9 mix 첨가 여부에 관계없이 TA98 균주 및 S9 mix 첨가TA100, TA1537, WP2uvrA(pKM101) 균주의 경우에는 생육저해가 관찰된 1,250 ${\mu}g/plate$를, S9 mix 미첨가의 TA1535 및 WP2uvrA(pKM101) 균주의 경우에는 2,500 ${\mu}g/plate$를 최고용량으로 하였고, 그 이하 공비 2로 최고용량을 포함한 5용량의 시험물질군과 음성대조군 및 양성대조군으로 하여 실험을 실시하였다. 그 결과, 모든 시험균주에서 시험물질에 의한 복귀변이 콜로니수는 S9 mix의 첨가 여부에 관계없이 용량의존적으로 증가되지 않았으며, 음성대조군과 비교하여 2배 이상의 증가를 보이지 않았다. 시험물질에 의한 균주의 생육저해는 S9 mix첨가 여부에 관계없이 사용한 모든 시험균주의 최고용량에서 관찰되었다. 시험물질의 석출은 S9 mix 첨가 여부에 관계없이 1,250 및 2,500 ${\mu}g/plate$에서 관찰되었지만 콜로니 계수에는 영향이 없는 것으로 나타났다.

• 한국축산식품학회지
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• 제18권3호
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• pp.203-208
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• 1998

The study was carried out to screen mutagenicity of smoking materials for the determination of optimum smoking temperature for meat products. Wood materials employed for smoking were oak and apple trees. Temperatures of the generator for manufacturing of smoke flavoring were set to 250$^{\circ}C$, 400$^{\circ}C$ and 500$^{\circ}C$, respectively. Mutagenic activities of smoke flavoring were assayed according to Ames test using Salmonella typhimurium TA98 and TA 100. In oak wood smoke flavoring, Salmonella typhimurium TA98 without S-9 mix showed strong mutagenic activities at the concentration of 6$\mu\textrm{g}$/plate(250$^{\circ}C$), 4$\mu\textrm{g}$/plate(400$^{circ}C$) and 6$\mu\textrm{g}$/plate(500$^{\circ}C$). Salmonella typhimurium TA100 with S-9 mix showed strong mutagenic activities at the concentration of 10$\mu\textrm{g}$/plate(250$^{\circ}C$), 20$\mu\textrm{g}$/plate(400$^{\circ}C$) and 10$\mu\textrm{g}$/plate(500$^{\circ}C$). Salmonella typhimurium TA98 with S-9 mix showed strong mutagenic activities at the concentration of 30$\mu\textrm{g}$/plate(250$^{\circ}C$), 40$\mu\textrm{g}$/plate(400$^{\circ}C$) and 20$\mu\textrm{g}$/plate(500$^{\circ}C$). Salmonella typhimurium TA100 with S-9 mix showed strong mutagenic activities at the concentration of 30$\mu\textrm{g}$/plate(250$^{\circ}C$), 50$\mu\textrm{g}$/plate(400$^{\circ}C$) and 20$\mu\textrm{g}$/plate(500$^{\circ}C$). Salmonella typhimurium TA100 without S-9 mix showed strong mutagenic activities at the concentration of 10$\mu\textrm{g}$/plate(250$^{\circ}C$), 20$\mu\textrm{g}$/plate(400$^{\circ}C$) and 20$\mu\textrm{g}$/plate(500$^{\circ}C$). Salmonella typhimurium TA98 with S-9 mix showed strong mutagenic activities at the concentration of 30$\mu\textrm{g}$/plate(250$^{\circ}C$), 40$\mu\textrm{g}$/plate(400$^{\circ}C$) and30$\mu\textrm{g}$/plate(500$^{\circ}C$). Salmonella typhimurium TA100 with S-9 mix showed strong mutagenic activities at the concentrations 30$\mu\textrm{g}$/plate(500$^{\circ}C$). Salmonella typhimurium TA100 with S-9 mix showed strong mutagenic activities at the concentration of 30$\mu\textrm{g}$/plate(250$^{\circ}C$), 20$\mu\textrm{g}$/plate(400$^{\circ}C$) and 30$\mu\textrm{g}$/plate(500$^{\circ}C$). From these results, it could be concluded that optimum smoking temperature for meat products should be set below 400$^{\circ}C$, that the compounds like benzo[a]pyrene etc. contain a variety of mutagenic potentials, which could be generated at the higher smoking temperature.

• Journal of Microbiology and Biotechnology
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• 제14권2호
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• pp.385-389
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• 2004

The antibody-mix sandwich enzyme-linked immunosorbent assay (Ab-mix sELlS A) system was developed in order to simultaneously detect the extracellular polysaccharide (FPS) of Aspergillus, Penicillium, or Fusarium species using one detection system. The detection limit and detection range of the Ab-mix sELISA towards EPS of Penicilliun citrinum were not changed, and those towards Fusarium moniliforme EPS were changed a little compared to that of individual sandwich ELISA [9, 10]. The fungal culture filtrates of Aspergillus and Penicillium species showed nearly similar reactivity towards Ab-mix sELISA as that of sELISA using the MAb lB8 alone [9]. Also, the fungal culture filtrates of Fusarium species showed nearly the same reactivity towards Ab-mix sELISA as that of sELISA using the MAb lB8 alone [10]. Thus, this ELISA system showed that the three genera of molds, Aspergillus, Penicillium, or Fusarium, which are three major important molds producing mycotoxins in food or agricultural commodities, could be detected at the same time, using one detection system.

• 대한본초학회지
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• 제25권1호
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• pp.1-7
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• 2010

Objectives : We investigated genetic toxicity of HMCO5 in relation to chromosome aberration test on Cultured Chinese Hamster Lung (CHL) in the presence and absence of S-9 mix. Methods : Experimental groups were divided into two groups: with S-9mix (+S) or without S-9 mix (-S). -S group was also divided 2 series by treatment hours (6 hr: 6-S; or 24 hr; 24-S). Each group treated with vehicle only (complete culture medium), HMCO5 (1,250, 2,500, $5,000\;{\mu}g/ml$), and cyclophosphamide monohydrate (CPA) and ethylmethanesulfonate (EMS), respectively. Results : HMC05 did not show any aberrant metaphase. However, there were significant (p < 0.01) aberrant metaphases with CPA in S+ and with EMS in S-. Conclusions : These results indicate that HMC05 formula does not show any toxicity in chromosome aberration test.

• 한국식품위생안전성학회지
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• 제16권2호
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• pp.133-138
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• 2001

우리나라 전통 장류의 위생화와 저장.유통안정성 확보를 위해 20 kGy 감마선 조사된 간장, 된장, 고추장, 청국장의 독성학적 안전성을 SOS Chromotest로 측정하였다. 대사활성계(S-9 mix) 존재 유무의 조건하에서 Escherichia coli PQ37을 SOS Chromotest 균주로 사용하였다. 시료는 물추출물, 용매추출물을 준비한 후 농축하여 S-9 mix를 첨가하거나 첨가하지 않은 조건에서 SOS Chromotes에 사용하였다. 결과적으로 10,00$\mu\textrm{g}$/assay의 투여 농도에서 1.5이하의 IF값을 유지했으며 조사된 모든 시료는 비조사구와 차이가 없었고, 20 kGy로 조사된 전통장류에서 어떠한 돌연변이원성도 발견되지 않았음을 확인할 수 있었다.

• 한국환경과학회지
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• 제10권1호
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• pp.35-39
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• 2001

The mutagenicity of the river water of Nakdong river estuary was determined by Ames test using the blue rayon suspension method. Samples were collected from 10 sites in the estuary once in each season of 1998. The samples collected from the sites where industrial waste discharge on May were mutagenic, but the other samples were not mutagenic. The sample collected from the site 1 located near the industrial area (Hadan-dong) were highly mutagenic in the TA98 with (+S9) and without (-S9) mix as well as in the TA100 with (+S9) and without (-S9) S9 mix, suggesting that the river water of this site is polluted by direct and indirect mutagens of frame-shift type as well as direct and indirect mutagens of base-replacement type. The positive mutagenicity, although relatively low, was also detected in TA98 with (+S9) and without (-S9) S9 mix in the extract of the site 4 near the industrial area(Jangrim-dong), suggesting that the primary mutation type is frame-shift. The negative mutagenicity from July to December at the sites (1-4) near the industrial area seems to be affected by the low economic growth rate in 1998 in Korea. On the other hand, the negative mutagenicity in all extracts collected from the sites 5-10 near the residential area where living sewage discharge, suggests that the river water was not polluted by mutagens.

• 대한간호학회지
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• 제27권3호
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• pp.520-530
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• 1997

Antineoplastic agents may exhibit effects not only in patients therapeutically exposed, but also in health workers who prepare and administer these drugs. This study was done to clarify whether nurses who handle anticancer drugs show signs of drug absorption. The experimental group was 14 nurses handling anticancer drugs at three medical wards of a hospital in J city ; the control group was 12 psychiatric nurses at the same hospital. The test materials were the nurses' 24hr urine specimens, which were concentrated by XAD-2 column chromatograpy. Tester strains were TA98(±S9mix), TA100(±S9 mix), TA1535(±S9 mix) and TA1537(±S9 mix) : the salmonella mammalian microsomal test (Ames test) was used for the urinary mutagenicity assay. The results are summarized as follow : 1. In qualitative analysis of the results, both experimental group and control group showed 15.4% urine toxicity. 2. The experimental group revealed significantly higher urinary mutagenicity both in the activation method test and non-activation method test of the tester strains TA98, TA100 and TA1535. In the case of TA1537, the two groups showed no difference in the non-activation method test, but the activation method revealed a difference. 3. In urinary mutagenicity of the experimental group by ward career, there was a significant difference between the group with more than 20 months experience and the group with less than 20 months on the tester strains TA98, TA100, and TA1537. No Significant difference was found between two groups by the tester strain TA1535.