• 제목/요약/키워드: Restriction enzyme profile

검색결과 13건 처리시간 0.025초

Phycocyanin locus내의 DNA Polymorphism에 의한 한국산 Cyanobacteria의 유전적 다양성 (Genetic Diversity of Korean Cyanobacteria determined by DNA polymorphisms within the Phycocyanin Locus)

  • 박진숙;권주리;유순애
    • 미생물학회지
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    • 제36권4호
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    • pp.249-253
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    • 2000
  • Cyanobacteria의 광합성 보조색소인 phycocyanin의 PC operon(cpc gene)을 PCR로 증폭하고, 제한효소로 처리하여 RFLP pattern을 비교하였다. Intergenic spacer sequence를 포함한 cpc gene은 실험에 사용한 cyanobacteria 균주 모두에게 증폭되었으며, 산물의 size는 약 700 bp였다. PCR산물을 5종의 제한효소로 처리한 결과 AluI, MspI, HaeIII는 같은 속내으ㅐ 균주간에 동일한 pattern을 나타내어 속 구분이 가능하였으며 CfoI은 Anabeana와 Synechocystis속의 균주간에 구별되는 양상을 나타내어 속내 균주 구별에 유용하였다. Restriction enzyme profile에 의한 phenogram에서 Anabeana, Chlorogloea, Synechyhocystis는 각각 하나의 cluster를 형성하여 cyanobacteria의 분류에 PC-IGS의 RFLP pattern이 유용함을 알 수 있었다.

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The New LM-PCR/Shifter Method for the Genotyping of Microorganisms Based on the Use of a Class IIS Restriction Enzyme and Ligation-Mediated PCR

  • Krawczyk, Beata;Leibner-Ciszak, Justyna;Stojowska, Karolina;Kur, Jozef
    • Journal of Microbiology and Biotechnology
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    • 제21권12호
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    • pp.1336-1344
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    • 2011
  • This study details and examines a novel ligation-mediated polymerase chain reaction (LM-PCR) method. Named the LM-PCR/Shifter, it relies on the use of a Class IIS restriction enzyme giving restriction fragments with different 4-base, 5' overhangs, this being the Shifter, and the ligation of appropriate oligonucleotide adapters. A sequence of 4-base, 5' overhangs of the adapter and a 4-base sequence of the 3' end of the primer(s) determine a subset of the genomic restriction fragments, which are amplified by PCR. The method permits the differentiation of bacterial species strains on the basis of the different DNA band patterns obtained after electrophoresis in polyacrylamide gels stained with ethidium bromide and visualized in UV light. The usefulness of the LM-PCR/Shifter method for genotyping is analyzed by a comparison with the restriction endonuclease analysis of chromosomal DNA by the pulsed-field gel electrophoresis (REA-PFGE) and PCR melting profile (PCR MP) methods for isolates of clinical origin. The clustering of the LM-PCR/Shifter fingerprinting data matched those of the REA-PFGE and PCR MP methods. We found that the LM-PCR/Shifter is rapid, and offers good discriminatory power and excellent reproducibility, making it a method that may be effectively applied in epidemiological studies.

동물에서 분리된 Salmonella균의 병원성 관련 Plasmid에 관한 연구 (Virulence-associated plasmids of Salmonella spp. isolated from animals in Korea)

  • 최원필;정석찬
    • 대한수의학회지
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    • 제32권3호
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    • pp.369-376
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    • 1992
  • This paper dealt with plasmid DNA profile in 98 Salmonella(S) isolated from pigs and cattle sources in Taegu, Gyeongbook and Gyeongnam during the period from 1984 to 1987. Also we were studied for restriction enzyme analysis of the plasmid DNA, and mouse infection, Sereny test and normal setum resistance test in guinea pig for S typhimurium and S enteritidis harbored or cured 60 megadalton(Md) plasmid and 36 Md plasmid, respectively. Of the 13 Salmonella isolated from cattle, 7 Salmonella harbored one or more plasmids and molecular sizes of the large plasmids were 60 Md for S typhimurium and 36 Md for S enteritidis. Of the 85 Salmonella isolated from pigs, 47 Salmonella were confirmed as being one or more plasmids, and all the S typimurium stains harbored 60 Md plasmid. In enzyme digestion with 8 types of restriction endonuclease for 60 Md plasmid DNA of S typhimurium, cleavage patterns were varied to enzymes, and the DNA was segmented into 4 to 15 fragments. In restriction enzyme analysis of 36 Md plasmid DNA obtained from four strains of S. enteritidis, the DNA showed the same cleavage patterns obtained with Eco RI, Hind III and Bam H I, and was segmented into 3 to 5 fragments. In virulence for mice by measuring the 50% lethal dose ($LD_{50}$), the $LD_{50}$ values obtained for 60 Md virulence-associated plasmid harbored strains of S typhimurium and 36 Md virulence-associated plasmid of S enteritidis were up to $10^4$-fold lower than the values obtained for the plasmid-cured strains of the same serotype. Only the plasmid harbored strains were resistant to the bactericidal activity of 90% guinea pig serum, and only they gave positive responses in sereny test. We suggested that their plasmid DNA might be associated with virulence for mice.

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표주박(Lagenaria leucantha var. gourda)에서 분리한 서브그룹 IB계통의 Cucumber mosaic virus (A Subgroup IB Isolate of Cucumber mosaic virus Isolated from Lagenaria leucantha var. gourda)

  • 오선미;홍진성;류기현;이긍표;최장경
    • 식물병연구
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    • 제15권3호
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    • pp.254-258
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    • 2009
  • 전형적인 모자이크 증상의 표주박(Lagenaria leucantha var. gourda)으로부터 CMV를 분리하고 Lag-CMV로 명명하였다. 표주박에서 분리한 Lag-CMV는 N. benthamiana에서 전신감염되어 전형적인 모자이크 증상을 나타내 대조로 공시한 CMV들과 유사하였다. 그러나 N. tabacum. cv. Xanthi nc에서 접종엽에 퇴록반점이 형성되는 점이 As-CMV와 유사하였으며, 접종엽에 무병징을 나타낸 Fny-CMV와 구분되었다. 또한 Fny-CMV에 감염된 오이와 쥬키니 호박은 매우 심한 모자이크 증상을 나타낸 반면, Lag-CMV와 As-CMV에 감염된 식물은 비교적 엷은 모자이크 병징이 발현되었다. 고추에서는 Fny-CMV와 As-CMV가 접종상엽에 모자이크 증상이 발현되으나, Lag-CMV는 무병징으로 감염되었다. Lag-CMV에 감염된 N. benthamiana로부터 추출한 dsRNA의 전기영동 패턴은 대조의 Fny-CMV나 As-CMV의 dsRNA와 종류 및 분자 크기에서 차이를 나타내지 않았다. Lag-CMV에 감염된 N. benthamiana로부터 추출한 total RNA를 외피단백질 유전자와 IR 및 3' 비번역영역 일부를 포함하는 약 950 bp의 cDNA합성을 위한 프라이머를 이용하여 RT-PCR을 실시한 결과 약 950 bp의 cDNA가 검출되었다. 이 cDNA를 제한효소 EcoRI, HindIII, MspI, SalI 및 XhoI으로 처리한 후 RFLP분석을 실시한 결과, Lag-CMV의 RFLP패턴은 As-CMV와 일치하였다. 한편 이 cDNA를 이용하여 염기서열을 분석한 결과, 염기서열의 유사도는 As-CMV와 99.1%, Fny-CMV와는 94.5%였으며, 외피단백질의 아미노산서열 유사도는 As-CMV는 100%, Fny-CMV와 97.3%를 나타냈다. 이와 같은 결과들로부터 표주박에서 분리한 Lag-CMV는 As-CMV와 같은 서브그룹 IB에 속하는 것으로 확인되었다.

A Novel Strain of Cucumber mosaic virus Isolated from Lilium longiflorum

  • Jung, Hye-Jin;Ueda, Shigenori;Ryu, Ki-Hyun;Lee, Sang-Yong;Choi, Jang-Kyung
    • The Plant Pathology Journal
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    • 제16권6호
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    • pp.306-311
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    • 2000
  • A new strain of Cucumber mosaic virus (CMV) from easter lily (Lilium longiflorum), Ly2-CMV, was identified and compared to the well-characterized Mf-CMV (subgroupⅠ) and LS-CMV (subgroupⅡ) by host reaction in several indicator plants, dsRNA analysis, serological property, RT-PCR analysis, restriction enzyme profile of the PCR products and nucleotide sequence of coat protein (CP) gene. Remarkable differences in symptoms of Ly2-CMV were found between Mf-CMV or LS-CMV in tobacco plants and Datura stramoinium. Ly2-CMV induced small necrotic ringspots on the inoculated leaves of Nicotiana tabacum cvs. Xanthi nc and Burley 21 and D. stramonium, and failed to infect these species systemically. Of the indicator plants tested, N. benthamiana only reacted with systemic infection by inoculation of Lr2-CMV. In experiments of dsRNA analysis, serology and RT-PCR of CP gene, Ly2-CMV was come within subgroupⅠ CMV. However, restriction enzyme analysis of the PCR products using MspⅠ showed that Ly2-CMV was distinct to Mf-CMV. The CP gene of Ly2-CMV contains 657 nucleotides, and the nucleotide sequence is similar to that of Mf-CMV. There is also a high degree of conservation between their putative gene products in Ly2-CMV and Mf-CMV, with five amino acid changes in the 218 amino acids of the CPs.

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과꽃에서 분리한 Cucumber mosaic virus의 성질 (Characterization of an Isolate of Cucumber mosaic virus Isolated from Chinese aster (Callistephus chinensis))

  • 오선미;김성률;홍진성;류기현;이긍표;최장경
    • 식물병연구
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    • 제14권3호
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    • pp.229-232
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    • 2008
  • 모자이크 증상의 과꽃(Callistephus chinensis L.)으로부터 Cucumber mosaic virus (CMV)의 한 계통(Cas-CMV)를 분리하고, Fny-CMV와 As-CMV를 대조로 기주반응, dsRNA, RT-PCR 및 RFLP분석을 통하여 바이러스를 동정하였다. Cas-CMV의 특징적인 기주반응의 차이는 박과 식물에서 발현되는 강한 병정이었으며, 특히 쥬키니호박에 접종하였을 때에는 접종 15-20일 후에 심한 모자이크 증상과 함께 어린 식물이 고사되는 괴저현상을 나타냈다. DsRNA분석과 RT-PCR실험의 결과는 Cas-CMV가 서브그룹 I의 CMV에 속하는 것으로 나타났으며, 더욱이 HindIII를 이용한 RFLP 분석은 Cas-CMV가 서브그룹 IA 구분되었다.

가금에서 분리한 Salmonella속 균의 항균물질에 대한 감수성 및 plasmid profile (Antimicrobial drug susceptibility and plasmid profiles of Salmonella species isolated from poultry)

  • 김원용;장영효;박경윤;김철중;신광순;박용하
    • 대한수의학회지
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    • 제35권3호
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    • pp.537-542
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    • 1995
  • In this study, we aim to find the presence of virulence-related plasmid in Salmonella isolates from poultry, and the difference between S pullorum and S gallinarum on the plasmid profile and antibiotics resistance. We used seventeen isolates of Salmonella spp that were isolated from poultry. Thirteen isolates, S typhimurium(ST), S pullorum(SP) and S gallinarum(SG), contained virulence-related plasmids. These are 95Kd plasmid in ST and 85Kd plasmid in SP and SG. Three(1/4 of ST, 1/1 of SE, and 1/9 of SP) isolates have no detectable plasmids. The isolates of ST have relatively variable plasmid profile but the isolates of S pullorum except No 12(additional 3.0Kb plasmid) have common 85K6, 8.1Kb, 4.0Kb and 2.3Kb plasmid and two of three isolates of S gallinarum have common 85Kb, 4.0Kb and 2.3Kb plasmid but the rest has only 85Kb plasmid. Interestingly, all of the isolates of SP have 8.1Kb plasmid, and same size of plasmid is also found in one of ST isolates. All of the isolates have the resistance to penicillin, chloramphenicol, rifampicin, streptomycin, sulfamethazine and some isolates show the resistance to ampicillin and tetracycline. There is no relatedness between plasmid profile and antibiotics resistance and no differences between SP and SG in antibiotics resistance. Therefore further differentiation of each isolates by restriction enzyme assay and, if possible, charaterization of each plasmid, especially, 8.1Kb plasmid in SP and ST, may be necessary.

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Characterization of Multidrug-resistant Salmonella enterica Serovar Typhimurium Isolated from Swine Sources

  • Suh Dong Kyun;Song Jae Chan
    • 대한의생명과학회지
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    • 제11권2호
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    • pp.115-119
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    • 2005
  • A total of 28 Salmonella enterica serovar Typhimurium isolated from diseased pigs and swine carcasses between 2001 and 2003 were characterized by the antimicrobial resistance profiles, PCR for detection of S. Typhimurium DT104 and pulsed-field gel electrophoresis (PFGE) with the restriction enzyme XbaI. All but one isolate presented multidrug resistance (MDR) to more than two antibiotics tested. A total of 11 resistance profiles were observed, and two phenotypes, ST and ASSuTG, were the most common among them. Two isolates were found to be S. Typhimurium DT104 isolates by PCR, and their resistance profile did not show the DT104 typical resistance type ACSSuT, but ACSSuTGK instead. PFGE identified 11 banding patterns in dendrogram, and three main clusters (designated A to C) were represented. Interestingly, sixteen of 19S. Typhimurium isolates belonging to cluster B showed an identical band pattern.

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제한효소 절편길이 다형성(T-RFLP) 분석기법을 이용한 손에 서식하는 세균의 군집조성 분석 (Profile Analysis of Bacteria in Human Hands Using the Terminal Restriction Fragment Length Polymorphism (T-RFLP) Analysis)

  • 박지선;김승범
    • 과학수사학회지
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    • 제11권4호
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    • pp.276-282
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    • 2017
  • 사건현장에서 얻어질 수 있는 증거물로써 현대 분자수준의 수사기법에 힘입어 많은 미세증거물들의 가치가 확인되고 있다. 이러한 미세증거물에는 DNA처럼 개인 식별에 유용한 물질들도 포함되어 있지만, 실제 현장에서 개별적인 특성을 나타내는 증거물만을 수집하는 것은 쉽지 않기 때문에 아직 응용되지 못하거나 발굴되지 않은 증거물 후보군에 대해 연구가 지속되어야 할 필요가 있다. 본 연구에서는 16명의 사람으로부터 손에서 서식하는 세균 군집을 채취하였으며 미생물군집분석방법 중 하나인 제한효소 절편길이 다형성(T-RFLP) 기법을 개인 식별에 활용할 수 있는지의 여부를 조사하였다. 그 결과, 16개의 서로 다른 electropherogram을 얻을 수 있었고, Staphylococcus속과 Bacillus 속을 포함하여 개인마다 종류와 조성의 차이를 보이는 다양한 세균 분류군들이 손바닥에 서식하고 있음을 확인하였으며, 이를 개인을 둘러싼 환경조건과 성별 등의 요인들을 연관하여 해석하고자 하였다.

족삼리 전침자극에 의한 흰쥐 hypothalamus의 유전자 발현 profile 분석 (Gene Expression Profile of Rat Hypothalamus Treated with Electroacupuncture at ST36 Acupoint)

  • 노삼웅;이기석;최기순;나영인;홍무창;신민규;민병일;배현수
    • 동의생리병리학회지
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    • 제18권4호
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    • pp.1041-1054
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    • 2004
  • Electroacupuncture (EA) has been reported to increase pain threshold, and to enhance the NK cell activity by up-regulation of IFN-γ and endogenous β-endolphin. For the purpose of understanding the molecular mechanism of EA stimulation, we analyzed the gene expression profile of rat hypothalamus, treated on Zusanli (ST36) with EA, in comparison with control group by oligonucleotide chip microarray (Affymetrix GeneChip Rat Neurobiology U34 Array) and real-time RT-PCR. Sprague-Dawley (S-D) male rats were stimulated at the Zusanli (ST36) acupoint in restriction holder. Simultaneously the control group was given only holder stress without EA stimulation. In order to prove the appropriateness of EA treatment, we measured spleen NK cell activity with standard 51Cr release assay. NK cell activity of EA group was significantly increased comparing to control group. The microarray and PCR results show that EA treatment up-regulates expression of genes associated with 1) nerve growth such as NGF induced factor A and VGF, 2) signal transduction such as 5HT3 receptor subunit, AMPA receptor binding protein and Na-dependent neurotransmitter transporter, and 3) anti-oxidation such as superoxide dismutase and glutathione S-transferase. In addition, the activity of the anti-oxidative enzyme, SOD of hypothalamus, liver and RBC was enhanced compared to that of control. The list of differentially expressed genes may implicate further insight on the mechanism of acupuncture effects.