• 한국작물학회:학술대회논문집
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• 한국작물학회 2017년도 9th Asian Crop Science Association conference
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• pp.113-113
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• 2017

Downy mildew (DM), caused by several species in the Peronosclerospora and Scleropthora genera, is a major maize (Zea mays L.) disease in tropical or subtropical regions. DM is an obligate parasite species in the higher plants and spreads by oospores, wind, and mycelium in seed surface, soil, and living hosts. Owing to its geographical distribution and destructive yield reduction, DM is one of the most severe maize diseases among the maize pathogens. Positional cloning in combination with phenotyping is a general approach to identify disease resistant gene candidates in plants; however, it requires several time-consuming steps including population or fine mapping. Therefore, in the present study, we suggest a new combination strategy to improve the identification of disease resistant gene candidates. Downy mildew (DM) resistant maize was selected from five cultivars using the spreader row technique. Positional cloning and bioinformatics tools identified the DM resistant QTL marker (bnlg1702) and 47 protein coding genes annotations. Eventually, 5 DM resistant gene candidates, including bZIP34, Bak1, and Ppr, were identified by quantitative RT-PCR without fine mapping of the bnlg1702 locus. Specifically, we provided DM resistant gene candidates with our new strategy, including field selection by the spreader row technique without population preparation, the DM resistance region identification by positional cloning using bioinformatics tools, and expression level profiling by quantitative RT-PCR without fine mapping. As whole genome information is available for other crops, we propose applying our novel protocol to other crops or for other diseases with suitable adjustment.

• 한국미생물·생명공학회지
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• 제14권2호
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• pp.133-137
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• 1986

원생동물인 Tetrahymena thermophila의 17S-rDNA구조 및 hygromycin 내성 기구에 대한 연구의 일부로서 hygromycin 내성변이주 hmr3의 17S-rDNA를 대장균의 vector pBR 322에 cloning하였다. 우선 rDNA는 hot phenol-cresol 용액으로 추출하여 제한효소 Hind III 처리로서 약 2.2kbp의 17S-rDNA를 agarose 전기영동상에서 분리하였다. 이를 pBR 322에 cloning하여 wild type의 17S-rDNA probe와 colony hybridization시켜 선별하였다. 그중 5-19 균주의 recombinant plasmid로부터 17S-rDNA 의 전사 orientation위치가 pBR322의 tetracyline내성 유전자 쪽으로 삽입되어 있는 것을 확인하였다.

• Archives of Pharmacal Research
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• 제21권4호
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• pp.470-474
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• 1998

A kanamycin producer, Streptomyces kanamyceticus IFO 13414 is highly resistant to kanamycin. Cloning of the kanamycin resistance genes in S. lividans 1326 with pIJ702 gave several kanamycin resistant transformants. Two transformants, S. lividans SNUS 90041 and S. lividan. SNUS 91051 showed similar resistance patterns to various aminoglycoside antibiotics. Gene mapping experiments revealed that plasmids pSJ5030 and pSJ2131 isolated from the transformants have common resistant gene fragments. Subcloning of pSJ5030 gave a 1.8 Kb gene fragment which showed resistance to kanamycin. Cell free extracts of S. lividans SNUS 90041, S. lividans SNUS 91051 and subclone a S. lividans SNUS 91064 showed kanamycin acetyltransferase activity. The detailed gene map is included.

• 고려인삼학회:학술대회논문집
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• 고려인삼학회 1990년도 Proceedings of International Symposium on Korean Ginseng, 1990, Seoul, Korea
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• pp.65-67
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• 1990

The sequence of ginseng peptide gene was designed and synthesized by the solid phase plasmid pUC19. Escherichia coli JM101 cells were transformed with above hybrid plasmids. Ampicillin resistant transformants were screened and identified by in situ colony hybridization and Southern blot techinques. Finally the gene sequencing was done by the Sanger dideoxy method using primer extension.

• Journal of Ginseng Research
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• 제14권2호
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• pp.207-209
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• 1990

The sequence of ginseng peptide gene was designed and synthesized by the solid phase phosphoramidiate method. Synthetic segments were isolated, pllrified and joined to the plasmid pUC19. E.icherichiu coli JM101 cells were transformed with above hybrid plasmids. AmpiciIBin resistant transformants were screened and identified by in situ colony hybridization and Southern blot techniques. Finally the gene sequencing was done by the Sanger dideoxy method using primer extension.

• 미생물학회지
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• 제30권1호
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• pp.42-46
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• 1992

본 연구는 제초제의 일종인 glyphosate에 저항성을 갖는 균주를 분리하고 그 유전자를 cloning 함으로써 glyphosate 에 저항성을 갖는 유용작물의 인위적 생성 가능성을 모색코자 하였다. 제초제가 처리된 토양환경으로 부터 glyphosate에 고도의 저항성을 나타내는 균주를 분리하였다. 분리된 균주를 동정한 결과 Pseudomonas cepacia로 밝혀졌으며 10mM의 glyphosate가 처리된 환경에서도 강한 내성을 갖는 것으로 나타났다. Glyphosate 저항성 유전자는 염색체상에 존재하는 것으로 판명되었으며 저항성 유전자를 클로닝한 결과 glyphosate 에 저항성을 나타내는 클론 (E. coli THG-101)을 얻었으며 P. cepacia 에서 유래된 glyphosate 저항성 유전자를 갖고 있는 plasmid pGR19를 확인하였다.

• 미생물학회지
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• 제22권4호
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• pp.229-234
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• 1984

A modified E. coli trp operon, $trpL({\Delta}att)\;trpE^{FBR}$, was conjugally transfered into Klebsiella pneumoniae $KC_{100}\;(Phe^-,\;Tyr^-,\;Trp^-,\;Rif^r,\;Kam^r)$ by in vivo cloning using the hybrid plasmid $R_{6}K::$ Mucts 61 with a transfer frequency of $5.2{\times}10^{-7}$. Two K. pneumoniae transconjugants, $KUA_{701}\;and\;KUA_{702}$, were isolated. The characters of attenuation control-free and resistance to feedback-inhibition which are characteristics of donor C. coli trp operon were normally expressed in the $KUA_{701}.\;However,\;KUA_{702}$ retained only the feedback-inhibition resistant character. $Trp^+$ phenotype and ampicillin resistant character were completely stable in the transconjugants, but streptomycin resistant character was lost in the transconjugants.

• 고려인삼학회:학술대회논문집
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• 고려인삼학회 2004년도 추계 학술대회 및 정기총회
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• pp.50-52
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• 2004

Introduce of gene connected with disease and transformation system of ginseng, Squalene systhase(PSS) gene cloned from and disease resistant gene were carried out for expression and transformation of plant using Agrobacterium. PSS of 35S-35S-AMV-PSS-Tnos, has been constructed which were mobilized into Agrobacterium tumefaciens strain MP 90 disarmed Ti-plasmid. PSS gene were introduced into the binary vector pRD 400. The transgenic ginseg plants were propagated using repetitive secondary embryogenesis and introduced NPTII and PSS genes of the transgenic ginseng were successfully indentified by the PCR and survival test on the medium.

• Journal of Microbiology and Biotechnology
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• 제23권3호
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• pp.430-435
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• 2013

Multidrug resistance, especially multidrug efflux mechanisms that extrude structurally unrelated cytotoxic compounds from the cell by multidrug transporters, is a serious problem and one of the main reasons for the failure of therapeutic treatment of infections by pathogenic microorganisms as well as of cancer cells. Streptococcus mutans is considered one of the primary causative agents of dental caries and periodontal disease, which comprise the most common oral diseases. A fragment of chromosomal DNA from S. mutans KCTC3065 was cloned using Escherichia coli KAM32 as host cells lacking major multidrug efflux pumps. Although E. coli KAM32 cells were very sensitive to many antimicrobial agents, the transformed cells harboring a recombinant plasmid became resistant to several structurally unrelated antimicrobial agents such as tetracycline, kanamycin, rhodamin 6G, ampicillin, acriflavine, ethidium bromide, and tetraphenylphosphonium chloride. This suggested that the cloned DNA fragment carries a gene encoding a multidrug efflux pump. Among 49 of the multidrug-resistant transformants, we report the functional gene cloning and characterization of the function of one multidrug efflux pump, namely MdeA from S. mutans, which was expressed in E. coli KAM32. Judging from the structural and biochemical properties, we concluded that MdeA is the first cloned and characterized multidrug efflux pump using the proton motive force as the energy for efflux drugs.

• 한국작물학회지
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• 제40권1호
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• pp.52-58
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• 1995

옥수수의 5-methyltryptophan 저 항성 돌연변이 주（MR1）로부터 anthranilate synthetase（AS）와 tryptophan synthetase（75）의 특성을 분석하였다. 대조구 식물로써 사용한 옥수수 품종 당진의 순계와 저항성주에 있어서 AS와 75의 효소 활성은 5-MT를 포함하지 않은 MS기본배지에서 생장시켰을 때는 차이를 보이지 않았다. 그러나, 25mg/L의 5-MT를 포함한 MS배지에서 생장한 MR1에 있어서 AS의 활성은 대조구보다 2배 높았다. 또한, 4mg/L의 L-tryptophan을 처리 했을때의 AS의 활성은 50％ 저해 되었다. MR1의 조추출물로부터 대조구와 동일한 활성저해율을 나타내기 위해서는 약 4배의 아미노산이 필요하였다. MR1의 75활성은 대조 식물보다 4배가 더 높았다. 그리 하여 tryptophan synthetase B subunit （TSB）를 encoding하는 유전자를 cloning하여 염기배열을 결정 하였다. TSB유전자는 상이한 기관으로부터 cloning된 TSB와 높은 상동성을 보였으며, 모든 발육단계에서 발현하였다. 띠orthern hybridization분석에서 MR1의 TSB발현량은 대조식물보다 높게 나타났다