• Journal of Applied Biological Chemistry
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• 제56권3호
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• pp.147-156
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• 2013

The objectives of this study were to investigate the effect of Lactobacillus paracasei subsp. tolerans JG22 isolated from pepper leaf jangajji on the mutagenic activity of N-methyl, N'-nitro, N-nitrosoguanidine (MNNG) and 2-nitrofluene (2-NF) and to evaluate the effect of physico-chemical pretreatment on the antimutagenic activity of the strain. The viable cells of JG22 strain displayed a significantly high (p <0.05) antimutagenic activity against both mutagens tested. The antimutagenic effect of JG22 strain seems to be positively correlated with the amounts of the cells in the incubation time. This strain produced the antimutagenic activity of the maximum levels after preincubation for 30 min. The binding of this strain against the mutagenic compounds might be mainly present in the cell wall fraction rather than the cytosol fraction. Pretreatment with proteolytic enzymes and simulated gastric and intestinal juices and at different pH values had no significant effect on two mutagens removal by the viable cells. However, the binding activity of the mutagen by the strain seems to be affected by heating, enzymes including $\alpha$-amylase and lysozyme, divalent ions, and sodium metaperiodate. Thus, carbohydrates consisting of the cell walls may be important elements responsible for the binding of MNNG and 2-NF by this strain. In conclusion, the binding of the mutagens to cells of JG 22 strain may play a vital role in suppressing the process of mutagenesis induced by mutagens.

• Preventive Nutrition and Food Science
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• 제3권4호
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• pp.334-338
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• 1998

Kale(Brassica oleracea var. acephala) is one of Cruciferous vegetables that is closely related to the wild ancestral form of cabbabe. The ethanol extract of kale which contains the active compoundsss under Salmonella assay system was fractionated with chloroform to collect the nonpolar solvent soluble compounds, and then further fractionation was carried out by silica gel column chromatography. Among kale extracts separated by silical gel column chromatography, the fractions of 4, 5 and 6 exhibited strong antimutagenic activities. The major active compounds from the fraction were identified as chlorophyll derivatives by the analysis with HPLC-fritp-MS. The molecular weights of each chlorophyll derivatives in the sample were acquired from the peaks of positive ion atomosphere pressure chemical ionization (APCI) mas spectrometry.

• Preventive Nutrition and Food Science
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• 제1권2호
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• pp.151-158
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• 1996

Antimutagenic effect of Doenjang (Korean soy paste) on various carcinogens in Salmonella typhimurium strains of TA98 and TA100 were studied. By the addition of methanol extract of Doenjang to aflatoxin B₁(AFB₁)in the experimental system, the mutagenicity of AFB₁ on the strains of TA98 and TA100 was com-pletely inhibited. The methenol extract of the Doenjang also inhibited the mutagencities induced by direct mutagens such as N-methy1-N'-nitro-N-nitroguanidine(MNNG)and 4-nitroquinoline-1-oxide(4-NQO), and another indirect mutagens of benzo(a) pyrene(BaP) and dimethylnitrosamine(DMN). From the solvents and thin layer chromatographic(TLC) fractionations, free fatty acid(s), especially linoleic acid in Doenjang seemed to be one of the active antimutagenic compounds.

• 한국지역사회생활과학회지
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• 제16권2호
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• pp.3-9
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• 2005

The study was carried out to evaluate the antimutagenic and anticancer effects of small water dropwort. The methanol extracts from small water dropwort significantly reduced the mutagenicity induced by aflatoxin $B_1\;(AFB_1)$ and N-methyl-N'-nitro-N-nitrosoguanidine(MNNG) in Salmonella typhimutium TA 100. Also, the methanol extracts inhibited the growth of AZ-521 human gastric cancer cells and HT-29 colon cancer cells. The chloroform fraction from methanol extracts of small water dropwort inhibited $40\;to\;80\%$ of the mutagenicity by $AFB_1$ in Sal. typhimurium TA 100 by the addition of 2.5 to $10\%$. To separate active compounds, the chloroform fraction was subjected to column chromatography on a silica gel and separated into five fractions. Among the five fractions, fraction 4 showed the highest antimutagenic effect against $AFB_1$ and an anticancer effect in the HT-29 colon cancer cell. As the result of the analysis in GC-MS, 1-napthalene carbonitrile, 5,6,7,8-tetrahydrol and benzene, 1,1'-(1,4-pentadiene-1,5-diyl) bis-,(E,E) were identified potentially from fraction 4.

• 한국식품과학회지
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• 제24권4호
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• pp.341-346
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• 1992

양송이(mushroom : Agaricus bisporus)로부터 polyphenol oxidase를 추출하여 4종류의 polyphenol 화합물과 반응시켜 양송이 효소 갈변반응생성물을 얻고, 이들 갈변물질들에 대하여 B. subtilis $H17(rec^+)$과 $M45(rec^-)$를 이용한 spore rec-assay, S. typhimurium TA98과 TA100을 이용한 Ames test 그리고 E. coli PQ37을 이용한 SOS chromotest를 실시하여 돌연변이원성 및 항돌연변이원성을 검토하였다. Spore rec-assay에서는 4가지 갈변물질 모두 B. subtilis $H17(rec^+)$과 $M45(rec^-)$ 두 균주에 대하여 생육저지대의 차이가 없었으므로 갈변물질 자체로서는 돌연변이원성이 없는 것으로 나타났으며, MNNG에 대한 항돌연변이원성 실험에서는 시료 모두 돌연변이에 대하여 억제활성을 나타내었으며 그중 HHQ-MEBRP는 가장 강한 억제활성을 나타내었다. Ames test에서는 4가지 시료 모두 돌연변이원성은 인정되지 않았으며, 항돌연변이원성 실험에서는 시료 $300\;{\mu}l$ 첨가시 $B({\alpha})P(20\;{\mu}g)$에 대하여 S. typhimurium TA98 및 TA100 두 균주에서 Ca-MEBRP와 HHQ-MEBRP는 $91{\sim}95%$, HCa-MEBRP와 Py-MEBRP는 $50{\sim}80%$의 억제활성을 나타내었다. $Trp-P-1(2\;{\mu}g)$에 대해서도 4가지 시료 모두 억제활성을 나타내었으며, HHQ-MEBRP는 TA98과 TA100 두 균주 모두에서 99%, HCa-MEBRP도 96%의 강한 억제활성을 나타내었다. SOS chromotest에서도 spore rec-assay와 Ames test에서와 같이 시료 자체의 돌연변이원성은 없는 것으로 나타났으며 4NQO와 MMC와 같은 돌연변이원물질에 의한 SOS-inducing function에 대하여 억제효과가 있었으므로 항돌연변이원성이 있음이 확인되었다.

• 한국식품과학회지
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• 제30권3호
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• pp.688-692
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• 1998

천연생리활성물질의 개발과 미이용자원의 효율적 재이용방안을 모색하기 위하여 13여종의 한국산 야생 버섯류를 에탄올과 물로 추출하여 각 시료추출물의 항변이원성 물질 검색을 시도하였다. B(a)P과 MNNG의 돌연변이 유발성에 미치는 야생버섯류의 에탄올 추출물과 물추출물의 항돌연변이 효과의 검토는 Salmonella typhimurium TA98과 TA100을 이용한 Ames 실험계를 이용하였으며 B(a)P에 대해 꽃구멍장이버섯(Polyporus dispansus), 깔때기꾀꼬리버섯(Cantharellus infundibuliformis), 진갈색주름버섯(Agaricus subrutilescens), 테미로버섯(Daedalea dickinsii), 목장말똥버섯 (Panaeolus papilionaceus) 및 턱수염버섯(Hydnum repandum) 등의 에탄올추출물에서 비교적 강한 항변이 원성을 나타내었다. 물추출물의 경우는 B(a)P에 대해서 턱수염버섯(Hydnum repandum)이 TA100에서 가장 강한 저해효과를 나타내었고 대부분의 시료는 낮거나 저해활성이 보이지 않았다. 직접변이원인 MNNG에 대해서는 야생버섯류의 에탄올추출물중 5종만 항변이원성이 관찰되었고, 물추출물의 경우는 꽃구멍장이버섯(Polyporus dispansus)이 가장 강한 저해효과를 보였으나 대부분의 버섯류는 낮거나 저해 효과를 거의 나타내지 않았다. 그중 직, 간접 변이원에 대해 가장 강한 저해 효과를 나타낸 꽃구멍장이 버섯의 에탄올추출물은 농도가 높을수록 항변이원성 효과가 증가하는 경향을 보였다.

• 한국식품과학회지
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• 제27권6호
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• pp.897-901
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• 1995

환삼덩굴의 생리활성물질을 구명하기 위하여 환삼덩굴을 물과 메탄올로 추출하여 돌연변이원성과 항돌연변이 효과를 조사하고 TLC와 HPLC로 flavonoid 성분을 분리하였다. 환삼덩굴의 물 추출물과 메탄올 추출물은 Salmonella typhimurium TA98과 TA100을 이용한 Ames test에서 돌연변이원성을 나타내지 않았다. 환삼덩굴의 메탄올 추출물은 NPD와 NQO로 돌연변이를 유도한 Salmonella typhimurium TA98과 TA100에 대하여 항돌연변이 효과를 나타내었다. 분획별 항돌연변이 효과는 헥산분획에서 높게 나타났으며 50% 돌연변이 억제농도($IC_{50}$)는 TA98에 대하여는 2.O mg/plate, TA100에 대하여는 0.5 mg/plate 였으며, 4.O mg/plate의 농도에서 TA98에 대하여는 약 58%, TA100에 대하여는 약 88% 정도의 돌연변이 억제활성을 나타내었다. 환삼덩굴의 에칠아세테이트 분획에서 quercitrin과 luteolin을 확인하였다.

• 한국환경성돌연변이발암원학회:학술대회논문집
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• 한국환경성돌연변이발암원학회 2001년도 Korean Environmental Mutagen Society
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• pp.10-10
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• 2001

• Applied Biological Chemistry
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• 제36권6호
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• pp.424-427
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• 1993

갓(Brassica juncea Cosson)의 chloroform추출물이 Salmonella typhimurium TA100균주에서 $AFB_1$의 돌연변이유발을 억제시키는 효과가있었으며, chloroform획분 중에 존재하는 화합물을 GC-MS로 분리/동정한 결과 4-decanol이 다량으로 함유되어있었다. 4-Decanol을 0.5%되게 DMSO에 녹인용액을 처리하였을 때 대조구에 비해 $AFB_1$과 MNNG의 돌연변이성을 각각 99%와 93%저해효과를 보이므로서 강한 항돌연변이 물질임이 밝혀졌다.

• Preventive Nutrition and Food Science
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• 제4권1호
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• pp.43-46
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• 1999

Taurine is known to suppress oxidant-induced tissue injury by stabilizing biomembrane and scavanging free radicals. The purpose of this study was to determne the antioxidative and antimutabenic acitvities of taurine, ad to compare those acitivities with major antioxidants. For the measurement of antioxidative capacity, 0.05 , 0.1,0.5 and 1.0mg/ml of taurine, L-Ascorbic acid, alpha-tocopherol, and BHT (dibuty hydroxiy toluene)were prepared and tested for their ability to donate electrons to DPPH (1,1-diphenyl-2-picryl-hydrazyl). Antimutagenic acitivity was examined using the Ames salmonela test system at concentrations of 600, 900 and 1200ug/ml. Results indicated that taurine possesses electron-donating capacity, however, the degree of donation was very weak compared to the major antioxidants tested. However, taurine was evaluated as a potent mutation suppressor. Antimutagenic capacity was in increasing order BHT>taurine>L-ascorbic acid>alpha-tocopherol at concentrations of 600 and 900ug/ml. There was a dose-dependent increase in antimutabenicity of these compounds , however, antimutagenity of the 900ug taurie/plate was not significantly differently from that of 1200ug taurine/plate. These results indicate that taurine effectively suppresses the mutagenicity of AFB1 without noticeable elelctron donating ability.