• 제목/요약/키워드: chemical mutagens

검색결과 74건 처리시간 0.02초

감마선 및 화학적 돌연변이원 처리가 스테비아 (Stevia rebaudiana Bert.)의 종자 발아 및 초기 생장에 미치는 영향 (Effects of Gamma-ray and Chemical Mutagens on the Germination and Seedling Growth in Stevia rebaudiana Bert.)

  • 윤태영;김이엽;김영호;최진수;현경섭;성윤희;조한직;김동섭;강시용;고정애
    • 방사선산업학회지
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    • 제6권2호
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    • pp.189-197
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    • 2012
  • This study was carried out to develop the improved useful mutants for yield or composition of stevia plants using the gamma ray or chemical mutagens treatments. The seeds of stevia 'Suwon No. 11' were irradiated up to 400 Gy of gamma ray. Chemical mutagens were treated on the seeds of the 'Suwon No. 11' using 0.07% colchicine, 10 mM sodium azide, or 10 mM NMU for various durations. The germination rate, and shoot and root growth of seedling were estimated at 30 days after gamma ray irradiation or chemical mutagen treatment, and the plant height, the number of branches, and leaf length and width were examined at 3 months after mutagenesis treatments. In the case of gamma ray treatments, the germination rate and early-stage growth were decreased as the increase of radiation dose, and the 50% lethal dose was found to be 200 Gy. the plant height was decreased as the increase of radiation dose, while the number of branches per plant and leaf length were increased. Leaf shape was modified to the relatively longer one compared to the control, which was identified more apparently at the treatments of higher than 150 Gy. In the treatment of chemical mutagens, the rate of germination and survival were decreased as the increase of incubation time. The 50% lethal dose for germination rate were identified as the conditions of the 15 hours incubation in 0.07% colchicine, the 4 hrs in 10 mM sodium azide, and the 2 hrs in 10 mM NMU, in the three chemical mutagens treatments. Chemical mutagens had no influence on shoot growth, while root growth was increased, especially as the incubation time was extended. The highest root growth occurred in the NMU treatment at 6 hrs incubation time. The plant height was decreased as the increase of incubation time in the chemical mutagens treatments. Among the chemical mutagens, NMU was the most effective to induce the mutants with long-shaped or the least lobed leaves.

화학 돌연변이제 이중처리에 의한 돌연변이율 향상 및 생장저해 경감 (Improvement of Mutation Rate and Reduction of Somatic Effects by Double Treatment of Chemical Mutagens in Barley)

  • 구본철
    • 한국작물학회지
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    • 제41권3호
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    • pp.348-353
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    • 1996
  • 1. 돌연변이처리후 실내에서 처리된 종자의 발아율, 제 1 엽 및 뿌리의 생장율을 보면 gamma ray나 화학제 처리된 Dema M$_1$, 유묘의 경우 생존율이 l~49%정도 감소하였고 Grosso의 경우는 그 감소의 폭이 Dema보다 적어 두 품종간의 돌연변이제에 대한반응의 차가 컸으며 같은 처리농도의 화학돌연변이제를 처리할 경우 두번에 나누어 중간의 휴지기를 두고 처리하는 것이 한 번에 처리하는 것보다 식물체의 생장 저해정도가 덜하였다. 2. 포장 M$_1$식물체의 간장의 감소율을 보면 화학약제의 경우 8.5~38.5%의 범위로 간장이 줄어들었으며 특히 1.5 mM의 MNH 처리시는 두 품종 모두 파종된 식물체가 고사하였고 0.75~l.0mM의 MNH처리시 15~38%심하였다. 그러나 이중처리할 때는 1.0~l.5mM이상의 고농도로 처리하여도 간장의 생장 감소율은 단일처리보다 상대적으로 덜 하였으며 이는 두 품종 모두 비슷한 경향이었다. 3. Dema에서는 gamma ray 180Gy처리시 간장의 감소가 28% 정도로 가장 심하였고 Grosso에서는 150Gy에서 13%로 가장 심한 경향이었다. 4. M$_2$식물체의 엽록소 돌연변이 발생율을 보면 화학약제나 방사선 처리 모두 처리강도가 높을수록 albino, xantha등의 엽록소 돌연변이체가 많이 나타났으며 약제의 이중 처리시 엽록소 돌연변이의 출현률이 다른 처리보다 높았다.

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노출기준 설정 화학물질의 CMR물질 정보 제공에 관한 연구 (A study on the provide of CMR substances information for Threshold Limit Values (TLVs) chemicals in KMoEL)

  • 이권섭;이혜진;이종한
    • 한국산업보건학회지
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    • 제22권1호
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    • pp.82-90
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    • 2012
  • Objectives: This study was performed to provide workplaces with political guidelines that apply international CMRs (Carcinogens, Mutagens, Reproductive toxins) information to Public Notice of TLVs (Threshold Limit Values). We analyzed information supply status about CMRs of international agencies and compared substances for which TLVs are set in KMoEL (Ministry of Employment and Labor in Korea). Methods: We referred to the reliable literature about classification criteria of CMRs corresponding to UN GHS (Globally Harmonized System of classification and Labeling of chemicals) and Public Notice No. 2009-68 'Standard for Classification, Labeling of Chemical Substance and Material Safety Data Sheet' in KMoEL. The classification system of CMRs in professional organizations (IARC, NTP, ACGIH, EU ECHA, KMoEL, etc.) was investigated through the internet and literature. Conclusions: 191 chemical substances among total 650 substances with TLVs are classified as carcinogens. Also, 43 substances classified as mutagens, and 44 as reproductive toxicants. These results suggest that the information of CMRs in Public Notice of TLV will be reorganized to 191 carcinogens, 43 mutagens, and 44 reproductive toxicants.

An Influence of Pretreatment Conditions on Mutagen Binding of Lactobacillus paracasei subsp. tolerans JG22 against MNNG and 2-NF

  • Lim, Sung-Mee
    • 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.

화학적 돌연변이원에 의한 Rhizopus nigricans의 돌연변이주 분리 (Isolation of Mutants in Rhizopus nigricans by Chemical Mutagens)

  • 신혜란;김명희;김말남
    • 한국균학회지
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    • 제21권3호
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    • pp.230-234
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    • 1993
  • R. nigricans Ehrenberg의 돌연변이주를 분리하기 위하여 화학적인 돌연변이원인 N-Methyl-N'-Nitro-N-Nitrosoguanidine(MNNG)과 Ethyl Methane Sulphonate(EMS)의 최적 처리 조건을 조사하였을 때, MNNG농도는 $125{\mu}g/ml$, 처리시간이 60분일 때 돌연변이율이 가장 높은 생존율 0.1-1.0%를 나타내었다. MNNG를 이용하여 영양요구성 돌연변이주 Leucine auxotroph를 분리하였으며, 포자낭병의 길이가 축소된 것, 포자낭병의 모양이 나선형으로 변한 것, 그리고 포자낭과 포자낭포자의 크기가 감소된 것 등 세 가지 형태적 변이주를 분리하였다.

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유색미 에탄올 추출물의 변이원성 및 화학적 직접변이원에 대한 항변이원 활성 검정 (Screening of Mutagenicity and Antimutagenic Activity against Chemical Direct Mutagens of Ethanolic Extracts from Colored Rice Bran)

  • 남석현;장수민;강미영
    • Applied Biological Chemistry
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    • 제45권4호
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    • pp.195-202
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    • 2002
  • 국내외에서 수집 재배한 29품종 유색미의 70% 에탄올 추출물로 세포독성, 변이원성, 화학적 직접변이원 mitomycin C, 4-nitroquinoline-N-oxide, 2,4,7-trinitro-9-fluorenone에 대한 항변이원성을 측정하였다. 세포 내재성 alkaline phosphatase활성을 지표로 유색미 추출물이 지시세포인 E. coli PQ 37의 성장에 미치는 영향을 조사한 결과 Jumlalocal, Jumlalocal-1을 포함하는 13종류의 유색미 추출물이 세포독성을 나타낸 반면 DK 1, SC-5, LK 1A-2-12-1-1및 wx 139-3-64-20-3-1등의 품종은 세포성장 촉진활성을 나타내었다. SOS chromotest 기법을 이용하여 유색미가 가지는 변이원성 및 항변이원성을 조사한 결과에서는 Jumlalocal-1, IR 17491-5-4-3-3 및 Jumlalocal 등의 품종이 변이원성을 유도하는 품종이었다. 화학적 직접변이원 mitomycin C, 2,4,7-trinitro-9-fluorenone 및 4-nitroquinoline-N-oxide 에 대해서 공통적으로 항변이원성 효과가 인정되는 유색미 품종은 LK1-3-6-12-1-1, Parnkhari 203, Jumlalocal, wx 139-3-64-20-3-1, Muthumanikam, HP 883-1-1-1-B-1-1, Jumla-local-1 등 7품종이었다.

Genotoxicity of the Herbicide 2,4-Dichlorophenoxyacetic acid (2,4-D): Higher Plants as Monitoring Systems

  • Enan, Mohamed R.
    • Journal of Forest and Environmental Science
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    • 제25권3호
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    • pp.147-155
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    • 2009
  • Higher plants provide valuable genetic assay systems for screening and monitoring environmental pollutants. They are now recognized as excellent indicators of mutagenic effects of environmental chemicals and are applicable for the detection of environmental mutagens both indoor and outdoor. 2,4-dichlorophenoxyacetic acid (2,4-D) is a herbicide commonly used in agriculture. The residues of 2,4-D are present in air, water, soil and edible plants. It constitutes a real hazard to the public health because it's wide spread use in agriculture. Genotoxic effects of 2,4-D on plant cells and potential of higher plants as a biomonitoring system for detecting chemical mutagens are evaluated. It is recommended that higher plant systems have been accepted by regulatory authorities as an alternative biomonitoring system for the detection of possible genetic damage resulting from pollution and the use of environmental chemicals.

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기내에서 화학돌연변이원 처리에 의한 참쇠고비의 변이주 유기 및 RAPD 분석 (Induction of Valiant of Cyrtomium caryoptideum var. coreanum Nakai by Chemical Mutagenesis In vitro and RAPD Analysis)

  • 정진아;이철희
    • 한국자원식물학회지
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    • 제19권2호
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    • pp.374-380
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    • 2006
  • 양치식물인 참쇠고비에서 인위적인 돌연변이를 유기하기 위하여, 기내배양한 근경조직에 EMS, NMU 등의 화학돌연변이원과 colchicine을 처리하였다. 식물체 재생률을 근거할 때, EMS의 적정 처리농도는 $20{\sim}50mM$이었으며, NMU는 $5{\sim}10mM$인 것으로 확인되었다. 또한 참쇠고비에서 엽의 색소 및 형태적 변이를 유도하는 데 있어 NMU가 EMS보다 효과적인 것으로 확인되었다. 표현형 변이 식물체의 유전적 변이를 분석하기 위하여 RAPD를 수행한 결과, 두 개의 10-mer primer에서 야생종과 변이주 사이에 다형성 DNA 밴드 패턴이 나타났다.

Photo-Ames Assay를 이용한 광발암성 예측 (Prediction of Photo-Carcinogenicity from Photo-Ames Assay)

  • Hong Mi Young;Kim Ji Young;Chung Moon Koo;Lee Michael
    • 한국환경성돌연변이발암원학회지
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    • 제25권1호
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    • pp.6-12
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    • 2005
  • Many compounds might become activated after absorption of UV light energy. In some cases, the resulting molecule may undergo further biological reaction of toxicological relevance related especially to the photo-carcinogenicity resulting from photo-genotoxicity. However, no regulatory requirements have been issued with the exception of guideline issued by the Scientific Committee of Cosmetology, Commission of the European Communities (SCC/EEC) on the testing of sunscreens for their photo-genotoxicity. Thus, the objectives of this study are to investigate the utility of photo-Ames assay for detecting photo-mutagens, and to evaluate its ability to predict rodent photo-carcinogenicity. Photo-Ames assay was performed on five test substances that demonstrated positive results in photo-carcinogenicity tests: 8-methoxypsoralen (photoactive substance that forms DNA adducts in the presence of ultraviolet A irradiation), chlorpromazine (an aliphatic phenothiazine an a-adr-energic blocking agent), lomefloxacin (an antibiotic in a class of drugs called fluoroquinolones), anthracene (a tricyclic aromatic hydrocarbon a basic substance for production of anthraquinone, dyes, pigments, insecticides, wood preservatives and coating materials) and retinoic acid (a retinoid compound closely related to vitamin A). Out of 5 test substances, 3 showed a positive outcome in photo-Ames assay. With this limited data set, an investigation into the predictive value of this photo-Ames test for determining the photo-carcinogenicity showed that photo-Ames assay has relatively low sensitivity (the ability of a test to predict carcinogenicity). Thus, to determine the use of in vitro genotoxicity tests for prediction of carcinogenicity,' several standard photo-genotoxicity assays should be compared for their suitability in detecting photo-genotoxic compounds.

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Cross-Coupling Reaction of 2-halo1-methyl-1H-imidazo[4,5-b]pyridine Offers a New Synthetic Route to Mutagenic Heterocyclic Amine-PHIP and DMIP

  • Sajith, Ayyiliath M.;Muralidharan, Arayambath;Karuvalam, Ranjith P.;Haridas, Karickal R.
    • 대한화학회지
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    • 제57권3호
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    • pp.361-364
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    • 2013
  • A modified synthetic approach to the synthesis of heterocyclic food mutagens, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PHIP) and 2-amino-1,6-dimethylimidazo[4,5-b]pyridine (DMIP) is reported. This route highlights an optimized palladium catalysed Buchwald cross-coupling of 2-halo-1-methyl-imidazo[4,5-b]pyridine with benzophenoneimine followed by acidic hydrolysis to yield compound 7. Using finely tailored conditions, Suzuki cross-coupling reactions with highly efficient catalytic systems were performed as the final step on 8 to introduce the aryl group and methyl group on the heterocyclic core.