• 제목/요약/키워드: genomic DNA extraction

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16S rDNA-DGGE를 이용한 2종의 제주도 해양 해면의 공생세균의 군집 구조 (Community Structure of Bacteria Associated with Two Marine Sponges from Jeju Island Based on 16S rDNA-DGGE Profiles)

  • 박진숙;심정자;안광득
    • 미생물학회지
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    • 제45권2호
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    • pp.170-176
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    • 2009
  • 제주도에 서식하는 2종의 해양 해면, Dictyonella sp.와 Spirastrella abata의 공생세균 군집구조를 16S rDNA-DGGE(denaturing gradient gel electrophoresis) 방법에 의해 분석하였다. 해면으로부터 total genomic DNA를 추출하여 GC clamp가 추가된 세균에 특이적인 341f primer와 518r primer를 이용하여 16S rRNA gene의 V3 부위를 증폭한 후 DGGE 전기 영동하고 재증폭하여 염기서열을 분석하였다. 그 결과 Dictyonella sp.에서 8개, Spirastrella abata에서 7개의 band를 확인할 수 있었다. 공통된 주요 band가 없는 패턴을 나타내었으며, DGGE band로부터 DNA를 추출하여 부분 염기서열을 분석한 결과, NCBI에 등록된 서열들과 93%~98%의 유사도를 나타내었다. Dictyonella sp.의 주요 해면 공생세균은 uncultured Gammaproteobacteria, Spirastrella abata의 경우 uncultured Alphaproteobacteria, Firmicutes에 각각 포함되어 해면 종에 따른 숙주 특이적 분포를 보이는 것으로 나타났다.

PCR-DGGE를 이용한 해양미생물의 다양성 조사 (Diversity of Marine Microbes by PCR-DGGE)

  • 김영진;조효진;유선녕;김광연;김형락;안순철
    • 한국수산과학회지
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    • 제40권6호
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    • pp.356-361
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    • 2007
  • Recently, the development of various culture-independent identification techniques for environmental microbes has greatly enhanced our knowledge of microbial diversity. In particular, denaturing gradient gel electrophoresis (DGGE) of 16S rDNA fragments, generated using the polymerase chain reaction (PCR) is frequently used to examine the diversity of environmental bacterial populations. This method consists of direct extraction of the environmental DNA, amplification of the 200-600 bp 16S rDNA fragments with universal primers, and separation of the fragments according to their melting point on a denaturing gradient gel. In this study, we investigated the seaside microbial community in coastal areas of Busan, Korea, using culture-independent techniques. First, marine genomic DNA was extracted from seawater samples collected at Songjeong, Gwangahn, and Songdo Beaches. Then, PCR was used to amplify the bacterial 16S rDNA using universal primers, and DGGE was used to separate the amplified 500 bp 16S rDNA fragments. Finally, the tested 16S rDNA genes were further analyzed by sequencing. Based on these experiments, we found that DGGE analysis clearly showed variation among the regional groups. It can be used to monitor rapid changes in the bacterial diversity of various environments. In addition, the sequence analysis indicated the existence of many unculturable bacteria, in addition to Arcobacter, Pseudoaltermonas, and Vibrio species.

비소세포폐암에서의 망막모세포종유전자의 소실 (Loss of the Retinoblastoma Gene in Non-Small Cell Lung Cancer)

  • 이춘택;김창민;조재일;심영목;홍원선;이진오;강태웅
    • Tuberculosis and Respiratory Diseases
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    • 제40권2호
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    • pp.98-103
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    • 1993
  • 연구배경 : Retinoblastoma 유전자(Rb)의 비활성화는 여러 종류의 암에서 관찰되어 왔다. Rb의 이형성의 소실(loss of heterozygosity)은 Rb의 비활성화의 가장 흔한 기전으로 소세포폐암에서는 거의 모든 예에서 관찰되나 비소세포폐암에서는 훨씬 낮은 빈도로 관찰된다고 알려져 있다. 이에 저자들은 개흉수술시 얻은 한국인의 비소세포폐암 및 정상폐조직의 DNA 에서 Rb의 변화를 관찰하였다. 방법: 폐암조직 및 정상폐조직에서 proteinase K에 의한 소화 및 phenol-chloroform 추출 방법으로 genomic DNA를 추출한 후 제한효소인 EcoRI으로 소화시키고 agarose gel 에서 전기영동분리시켰다. Southern blot 방법으로 DNA를 nylon 막에 흡착시킨 후 Rb 1 탐식자로 hybridization 시켜 stringent condition에서 세척하여 X-ray 필름에 적당기간 노출시켜 현상하였다. 결과 : 26예의 편평상피세포암중 16예에서 정상폐 DNA 에서 RFLP에 의한 Rb의 이형성이 관찰되었으며 이중 10예 (62.5%)의 폐암조직 DNA 에서 이형성의 소실이 관찰되었다. 17예의 폐선암중 11예의 정상폐 DNA 에서 RFLP에 의한 Rb의 이형성이 관찰되었으며 이중 5예 (45.4%)의 폐암 DNA 에서 이형성의 소실이 관찰되었다. Rb의 비활성화 유무에 따른 두 군 사이에 연령, 성별, 암의 병기, 암의 분화도 및 흡연력의 차이가 없었다. 결론: 이상의 결과로 Rb의 비활성화는 비소세포폐암의 발생기전에 중요한 역할을 하리라 생각된다.

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Bacterial Community and Diversity from the Watermelon Cultivated Soils through Next Generation Sequencing Approach

  • Adhikari, Mahesh;Kim, Sang Woo;Kim, Hyun Seung;Kim, Ki Young;Park, Hyo Bin;Kim, Ki Jung;Lee, Youn Su
    • The Plant Pathology Journal
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    • 제37권6호
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    • pp.521-532
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    • 2021
  • Knowledge and better understanding of functions of the microbial community are pivotal for crop management. This study was conducted to study bacterial structures including Acidovorax species community structures and diversity from the watermelon cultivated soils in different regions of South Korea. In this study, soil samples were collected from watermelon cultivation areas from various places of South Korea and microbiome analysis was performed to analyze bacterial communities including Acidovorax species community. Next generation sequencing (NGS) was performed by extracting genomic DNA from 92 soil samples from 8 different provinces using a fast genomic DNA extraction kit. NGS data analysis results revealed that, total, 39,367 operational taxonomic unit (OTU), were obtained. NGS data results revealed that, most dominant phylum in all the soil samples was Proteobacteria (37.3%). In addition, most abundant genus was Acidobacterium (1.8%) in all the samples. In order to analyze species diversity among the collected soil samples, OTUs, community diversity, and Shannon index were measured. Shannon (9.297) and inverse Simpson (0.996) were found to have the highest diversity scores in the greenhouse soil sample of Gyeonggi-do province (GG4). Results from NGS sequencing suggest that, most of the soil samples consists of similar trend of bacterial community and diversity. Environmental factors play a key role in shaping the bacterial community and diversity. In order to address this statement, further correlation analysis between soil physical and chemical parameters with dominant bacterial community will be carried out to observe their interactions.

PCR-Based Assay for Rapid and Specific Detection of the New Xanthomonas oryzae pv. oryzae K3a Race Using an AFLP-Derived Marker

  • Song, Eun-Sung;Kim, Song-Yi;Noh, Tae-Hwan;Cho, Heejung;Chae, Soo-Cheon;Lee, Byoung-Moo
    • Journal of Microbiology and Biotechnology
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    • 제24권6호
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    • pp.732-739
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    • 2014
  • We describe the development of a polymerase chain reaction method for the rapid, precise, and specific detection of the Xanthomonas oryzae pv. oryzae (Xoo) K3a race, the bacterial blight pathogen of rice. The specific primer set was designed to amplify a genomic locus derived from an amplified fragment length polymorphism specific for the K3a race. The 1,024 bp amplicon was generated from the DNA of 13 isolates of Xoo K3a races out of 119 isolates of other races, pathovars, and Xanthomonas species. The assay does not require isolated bacterial cells or DNA extraction. Moreover, the pathogen was quickly detected in rice leaf 2 days after inoculation with bacteria and at a distance of 8 cm from the rice leaf 5 days later. The results suggest that this PCR-based assay will be a useful and powerful tool for the detection and identification of the Xoo K3a race in rice plants as well as for early diagnosis of infection in paddy fields.

한국인에 있어서 Actinobacillus actinomycetemcomitans의 가족내 전이양상에 관한 연구 (INTRAFAMILIAL TRANSMISSION OF ACTINOBACILLUS ACTINOMYCETEMCOMITANS IN KOREAN POPULATIONS)

  • 정영인;김성조;최점일
    • Journal of Periodontal and Implant Science
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    • 제25권3호
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    • pp.679-693
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    • 1995
  • The present study has been performed to see the intrafamilial transmission of periodontopathic organism Actinobacillus actinomycetemcomitans in Koreans having various froms of periodontal diseases. 17 clinical isolates from 8 periodontal patients and 20m clinical isolates from their 8 family members were grown anaerobically for the serotyping and the extraction of genomic DNA. The DNA was digested with restriction endonucleases (EcoRI+HindIII) and plasmid pAA 2097(kindly provided by Dr. DiRienzo, Univ. of Pennsylvania) including 4.7kb-size randlomly clone probe for restriction length pleomorphism analysis(RFLP). RFLP patterns of reference serotypes a, b, c, d, and e were used as the genotypes A, B, C, D, and E, respectively for comparison of genotypes of clinical isolates. 28 out of total 37 clinical isoltes belonged to either one of 5 basic gentotypes and 9 remaining isolats did not fall into any types, and hence were designate as non-type(NT). Genotype C were the most frequently found one(35.1%) and genotype B has not isolated. Intrafamilial transmission of bacteria between spouses, brothers and sisters, and parents and their offsprings, resepctively could well be demonstrated by comparing RFLP patterns. There were not any specific genotypes which showed predominance over others in terms of transmission.

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A Study on SNP of IL10 in Cerebral Infarction Patients

  • Jung, Tae-Young;Choi, Sung-Hun;Kim, Kyung-Woon;Lee, Yoon-Kyung;Lim, Seong-Chul;Lee, Kyung-Min;Seo, Jung-Chul
    • Journal of Acupuncture Research
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    • 제23권2호
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    • pp.173-179
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    • 2006
  • Objectives : In this study, we investigated the SNP (single-nucleotide polymorphism) of IL10 in patients with stroke. The present study was undertaken to see if specific genotypic and allelic variations are associated with stroke in the Korean population. Methods : Blood samples from all subjects were obtained for DNA extraction and collected in EDTA tube. Genomic DNA was extracted using DNA isolation kit for Mammalian Blood (Boehringer Mannheim, IN, USA). The extracted DNA was amplified by polymerase chain reaction (PCR). Pyrosequencing was performed according to manufacturer's standard protocol. Results : There was no statistically significant genotypic distribution difference between control and stroke group. The frequencies of A/A homozygotes and A/C heterozygotes among control subjects were 91 (87.5%) and 13 (12.5%). The frequencies of A/A and A/C among the stroke patients were 85 (89.5%) and 10 (10.5%). There was not statistically significant allelic frequency difference between control and stroke group. The allelic frequency of A and C was 195 (93.8%) and 13 (6.2%) among the control subjects and 180 (94.7%) and 10 (5.3%) in stroke patients, respectively. Conclusion : The cytokine IL10 may not be pathogenetic factors in stroke. But further studies including different cytokine gene can be a useful for predicting stroke. Establishment of more systemic approach and high quality of prospective cohorts will be necessary for the good prediction of genetic markers.

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석회유황합제가 배나무 낙엽의 진균 다양성 변화에 미치는 영향 (Effect of Lime Sulfur on Changes of Fungal Diversity in Pear Fallen Leaves)

  • 민광현;송장훈;조백호;양광열
    • 한국균학회지
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    • 제43권4호
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    • pp.281-285
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    • 2015
  • 석회유황합제의 배나무 동계방제 수단으로써 효과를 과학적으로 증명하기 위해 배 과수원에서 1차 전염원의 역할을 하는 낙엽에 석회유황합제를 처리한 후 낙엽에 존재하는 진균의 다양성 변화를 확인하였다. 물이 처리된 대조구와 석회유황합제 처리구의 낙엽에서 진균 genomic DNA를 추출한 다음 rDNA internal transcribed spacer (ITS) 영역의 염기서열 분석을 통해 진균들을 동정한 결과, 대조구와 석회유황합제 처리구에서 자낭균문(Ascomycota)과 담자균문(Basidiomycota)에 속하는 다양한 종류의 진균들이 동정되었으나 동정되는 진균의 수와 비율은 서로 다르게 나타났다. 특히 배 과피얼룩병을 일으키는 Alternaria속과 Cladosporium속의 진균은 대조구에 비해 석회유황합제 처리구에서 동정되는 비율이 대폭 감소되었으며, Phomopsis속의 진균은 대조구에서는 동정되었으나 석회유황합제 처리구에서는 동정되지 않았다. 이러한 결과는 석회유황합제 처리가 배 낙엽에 존재하는 진균 다양성의 변화에 영향을 미쳤으며 동계방제로서 역할을 수행할 수 있음을 시사한다.

Effective High-Throughput Blood Pooling Strategy before DNA Extraction for Detection of Malaria in Low-Transmission Settings

  • Nyunt, Myat Htut;Kyaw, Myat Phone;Thant, Kyaw Zin;Shein, Thinzer;Han, Soe Soe;Zaw, Ni Ni;Han, Jin-Hee;Lee, Seong-Kyun;Muh, Fauzi;Kim, Jung-Yeon;Cho, Shin-Hyeong;Lee, Sang-Eun;Yang, Eun-Jeong;Chang, Chulhun L.;Han, Eun-Taek
    • Parasites, Hosts and Diseases
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    • 제54권3호
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    • pp.253-259
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    • 2016
  • In the era of (pre) elimination setting, the prevalence of malaria has been decreasing in most of the previously endemic areas. Therefore, effective cost- and time-saving validated pooling strategy is needed for detection of malaria in low transmission settings. In this study, optimal pooling numbers and lowest detection limit were assessed using known density samples prepared systematically, followed by genomic DNA extraction and nested PCR. Pooling strategy that composed of 10 samples in 1 pool, $20{\mu}l$ in 1 sample, was optimal, and the parasite density as low as $2p/{\mu}l$ for both falciparum and vivax infection was enough for detection of malaria. This pooling method showed effectiveness for handling of a huge number of samples in low transmission settings (<9% positive rate). The results indicated that pooling of the blood samples before DNA extraction followed by usual nested PCR is useful and effective for detection of malaria in screening of hidden cases in low-transmission settings.

북극 스발바드 군도 콩스피요르드에서 채집한 해조류 추출물의 항산화 활성 (Antioxidant Activity of Seaweed Extracts from Kongsfjorden, an Inlet in the Arctic's Svalbard Archipelago)

  • 이정임;김유아;공창숙;예성수;한태준;강성호;김지희;서영완
    • Ocean and Polar Research
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    • 제31권2호
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    • pp.213-218
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    • 2009
  • We examined the intracellular antioxidative effects of 20 Arctic seaweed extracts in Raw 264.7 cells. Each seaweed species was subjected to extraction using acetone/dichloromethane and methanol, respectively, after which the extracts were combined and used as the test sample. The antioxidant ability of all 20 seaweeds extracts was evaluated using four different activity tests, including the degree of occurrence of intracellular reactive oxygen species (ROS), $ONOO^-$, and lipid peroxidation in Raw 264.7 cells, as well as the extent of oxidative damage of genomic DNA purified from Raw 264.7 cells. Crude extracts from Monostroma obscurum, Alaria esculnta, Laminaria digitata, Desmarestia aculeata, Chorda filum, Ptilota seriata, Phycidrys rubens, Devaleraea ramentacea and Palmaria palmata exhibited significant scavenging effects on the generation of intracellular ROS. Among them, Monostroma obscurum and Phycidrys rubens significantly inhibited membrane lipid peroxidation and DNA oxidation. Moreover, Phycidrys rubens exhibited scavenging effects on peroxynitrite generated from SIN-1.