• 한국초지조사료학회지
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• 제20권2호
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• pp.103-108
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• 2000

To produce of transgenic orchardgrass, the seed-derived calli of orchardgrass (Dactylis glomerata L.) co-cultivated with Agrobacterium turnefaciens EHAlOl harboring binary vector pIG121-Hm were selected with hygromycin and then transferred onto N6 regeneration medium containing 1 rngl l of NAA, 5 rngl l of kinetin, 250 rngl l of carbenicillin and 50 mg/ l of hygromycin. The efficiency of transformation was differed on cultivars, that is, 'Potomac' appeared 12% of transformation efficiency while 'Amba' did 5.5%. The addition of acetosyringone during co-cultivation was a key to successhl transformation of orchardgrass. Transgene fragments were identified by PCR analysis and the constitutive expression of GUS gene was confirmed by Northern blot analysis. (Key words : Acetosyringone, Agrobacterium tumefaciens, Orchardgrass (Dactylis glomerata L.), Transformation)

• 한국미생물·생명공학회지
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• 제27권4호
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• pp.339-343
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• 1999

Pasteurella haemolytica is well known to cause severe pneumonia, consolidation and oedema of the lung, and fibrinous pleurisy under the stress and infection of virus in the cattle. In the course of our screening for antimicrobial agents against P.haemloytica, compound 51086 has been isolated from the fermentation broth of Streptimyces sp. 51086. The compound 51086 was purified by SiO2, Sephadex LH-20 and ODS column chromatographies and HPLC, subsequently. The structure of compound 51086 was determined as hygromycin A by combination of 1H NMR, 13C NMR, HMBC, and ESI-MS. This compound showed significant antibacterial activity against P.haemolytica and P.multocida.

• 아시안잔디학회지
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• 제18권4호
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• pp.211-219
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• 2004

Transgenic zoysiagrass (Zoysia japonica cv. Zenith) plants have been obtained by particle bombardment of embryogenic callus with the plasmid pSMABuba, which contains hygromycin resistance (hpt) and bialaphos resistance (bar) genes. Parameters on DNA delivery efficiency of the particle bombardment were partially optimized using transient expression assay of a chimeric $\beta-glucuronidase$(gusA) gene driven by the CaMV 35S promoter. Stably transfarmed zoysiagrass plants were recovered with a selection scheme using hygromycin. Transgenic zoysiagrass plants were confirmed by PCR analysis with specific primer for bar gene. Expression of the transgene in transformed zoysiagrass plants was demonstrated by Reverse transcriptase (RT)-PCR analysis. All the tested transgenic plants showed herbicide BastaR resistance at the field application rate of $0.1\%-0.3\%$.

• ALGAE
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• 제28권4호
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• pp.379-387
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• 2013

The purpose of this study was to express bovine lactoferrin N-lobe in Chlorella vulgaris, a green microalga, using the pCAMBIA1304 vector. Chlorella-codon-optimized bovine lactoferrin N-lobe (Lfb-N gene) was cloned in the expression vector pCAMBIA1304, creating the plasmid pCAMLfb-N. pCAMLfb-N was then introduced into C. vulgaris by electro-transformation. Transformants were separated from BG-11 plates containing 20 ${\mu}g\;mL^{-1}$ hygromycin. Polymerase chain reaction was used to screen transformants harboring Lfb-N gene. Finally, total soluble protein was extracted from the transformants, and the expression of Lfb-N protein was detected using western blotting. Using this method, we successfully expressed bovine lactoferrin in C. vulgaris. Therefore, our results suggested that recombinant lactoferrin N-lobe, which has many uses in the biomedical and pharmaceutical industries, can be produced economically.

• Journal of Plant Biotechnology
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• 제30권3호
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• pp.233-239
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• 2003

We have developed a reliable and high-frequency genetic transformation and regeneration system via somatic embryogensis of Eleutherococcus sessiliflorus. Embryogenic callus obtained from seed were co- cultivated with Agrobacterium tumefaciens strain EHA101/pIG121Hm harboring genes for intron-$\beta$-glucoronidase(GUS), kanamycin and hygromycin resistance. Following co-cultivation, two types of samples(fine embrogenic calli and early globular embryo clusters) were cultivated on Murashige and Skoog(MS) medium containing 1 mg/L2.4-D for 3day in dark. Transient expression of GUS gene was found to be higher in the early globular embryo clusters than in the embryogenic calli. Also, co-cultivated period affected expression of GUS gene; the best result was obtained when globular embryo clusters were co-cultivated with Agrobacterium for 3 days. Subsequently, this callus transferred to selective MS medium containing 1mg/L2.4-D, 50mg/L kanamycin or/and 30mg/L hygromycin and 300mg/L cefortaxime. These embryogenic calls were subcultured to the same selection medium at every 2 weeks intervals. Approximately 24.5% of the early globular embryos co-cultivated with Agrobacterium for 3days produced kanamycin or/and hygromycin-resistant calli. Transgenic somatic embryos were converted into plantlets in half strength MS medium supplemented with 3mg/L GA$_3$ kanamycin and were confirmed by GUS histochemical assay and polymerase chain reaction analysis. Genomic Southem blot hybridization confirmed the incorporation of NPT II gene into the host genome.

• Journal of Periodontal and Implant Science
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• 제32권3호
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• pp.603-614
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• 2002

Human gingival fibroblasts have proven to useful as a species specific cell culture system in various system on periodontal disease and regeneration. However, their use is limited, since they are hard to obtain and lifespan is short due to replicative senescence. To overcome these disadvantages, we transfected primary human gingival fibroblasts by the E6 and E7 genes of the Human papilloma virus(HPV) 16. The full length of HPV 16 E6 and E7 was cloned from the pBR322 into BamHl and Sal I of a pBabe vector including hygromycin B resistance. Before pBabeE6/E7 plasmid transfection, peak 8 GFP including G418 resistance was transfected into primary GF to check the transfection efficency. PBabe E6/E7 plasmid was transfected using Lipofectamine plus following manufacter's instruction into primary normal human gingival fibroblasts in 60mm dishes with FBS free DMEM. After 2 days of transfection, the cells were treated with hygromycin for 2 weeks until the transfected control cells died. The resulting hygromycin resistant colonies were pooled, and clonned, and sucessful　transfection was established for immortalized gingival fibroblast cell lines. Immoralized GF cells showed stellate shape, that is similar to that of orange grains, and more rapid growth and higher proliferation than that of primary gingival fibroblasts. This cell lines overcame crisis and could be cultured over 30 subcultured, could be use for three dimentional culture, epithelial-mesenchymal interaction study.

• Journal of Microbiology
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• 제44권4호
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• pp.383-395
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• 2006

Four different Trichoderma strains, T. harzianum CECT 2413, T. asperellum T53, T. atroviride T11 and T. longibrachiatum T52, which represent three of the four sections contained in this genus, were transformed by two different techniques: a protocol based on the isolation of protoplasts and a protocol based on Agrobacterium-mediated transformation. Both methods were set up using hygromycin B or phleomycin resistance as the selection markers. Using these techniques, we obtained phenotypically stable transformants of these four different strains. The highest transformation efficiencies were obtained with the T. longibrachiatum T52 strain: 65-70 $transformants/{\mu}g$ DNA when transformed with the plasmid pAN7-1 (hygromycin B resistance) and 280 $transformants/l0^7$ spores when the Agrobacterium-mediated transformation was performed with the plasmid pUR5750 (hygromycin B resistance). Overall, the genetic analysis of the transform ants showed that some of the strains integrated and maintained the transforming DNA in their genome throughout the entire transformation and selection process. In other cases, the integrated DNA was lost.

• 한국균학회지
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• 제38권1호
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• pp.48-53
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• 2010

팽이버섯의 다양한 유전자의 기능을 연구하기 위한 방법으로 팽이 자실체의 주름조직을 사용하여 A. tumefaciens을 매개로 한 형질전환을 수행하였다. Hygromycin 항생제 저항성 유전자를 포함하고 있는 AGL-1 pBGgHg를 팽이버섯의 자실체 조직에 도입시킴으로서 형질전환체들을 얻을 수 있었다. 형질전환체 선발은 첫 번째로 hygromycin 선발 배지에서 선발한 뒤 gpd-FH, hph-R primer를 이용하여 PCR로 확인 할 수 있었다. hygromycin은 30 ug/ml에서 선발 효율이 가장 높았다. 형질전환체 중 일부는 갈색 자실체를 갖는 wild type과는 달리 백색 자실체를 나타내었다. 형질전환체의 southern blot결과 외래유전자가 팽이버섯 내부에 하나 또는 그 이상의 다양한 copy 수로 삽입되어 있음을 알 수 있었다. 또한 삽입된 유전자의 주변 염기서열에 대한 정보는 Inverse PCR을 통해 알 수 있었다.

• Applied Biological Chemistry
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• 제39권1호
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• pp.25-31
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• 1996

식물체내 칼모듈린과 칼모듈린 메틸화의 기능에 대한 정보를 얻기 위하여 칼모듈린 유도체($lys{\rightarrow}ile\;115$ 칼모듈린)를 발현시킬 수 있고 하이그로마이신(Hygromycin) 내성을 보일 수 있는 형질전환 담배 식물체와 하이그로마이신 내성만 보일 수 있는 형질전환 담배 식물체(대조구)가 Agrobacterium-mediated 형질전환을 통해 만들어 졌다. 이들 형질전환 담배 식물체로 부터 얻은 씨앗의 하이그로마이신 내성과 민감성에 대한 비는 예상대로 3 : 1을 보였다. Western blot과 Chemiluminescence 방법을 병행하여 형질전환 식물체($F_1$)의 잎으로 부터 칼모듈린 단백질을 검출한 결과 칼모듈린 단백질이 발현 되었음이 확인되었다. 두 형질 전환 담배 식물체로 부터 얻은 씨앗의 발아에 미치는 표피살균제의 영향을 조사해본 견과 칼모듈린 형질전환체의 씨앗은 살균수의 처리만으로도 MS 배지에서 씨앗 주변에 곰팡이 등의 오염없이 정상 발아되었으며, 대조구는 살균수와 차아염소산나트륨 용액(유효 염소 함유량 4%)을 1 : 1 배합하여 처리해주어야 오염으로 부터 벗어날 수 있었다. 칼모듈린 유도체를 발현 시키는 담배 씨앗과 대조구 담배 씨앗의 발아에 미치는 칼슘 농도의 영향을 조사해본 결과 저 농도의 칼슘을 함유한 MS배지에서는 초기 발아율에 있어 별 차이가 없었지만 고농도(예, 30mM)의 칼슘 함유배지에서는 칼모듈린 형질전환체 씨앗의 발아가 대조구 형질전환 식물체 씨앗의 발아에 비해 월등하게 잘 되었다. 이와 같은 결과들로 부터 칼모듈린 유도체의 담배 세포내 발현은 각종 환경적 요인에 대한 담배 씨앗의 적응능력을 증진시키는 것으로 제안할 수 있겠다.

• 식물조직배양학회지
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• 제22권3호
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• pp.175-182
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• 1995

벼는 임성 식물체의 재분화 뿐만 아니라 유전적으로 안정된 형질전환 식물체를 얻을 수 있는 가장 성공적인 단자엽 식물중 하나이다. 그러나 우리나라에서는 아직 유전적으로 안정된 임성 형질전환 벼품종에 대한 보고가 없었다. 본 연구에서 우리나라의 재배종인 낙동벼로부터 임성 형질전환식물체를 얼을 수 있음을 증명하였다. 현탁뱅양세포로부터 분리된 원형질체를 이용하여 PEG로 HPT와 GUS Plasmids늘 함께 형질전환시켰다. 다섯번의 실험을 통하여 hygromycin 저항성 캘러스는 평균 1.73%이였다. 소식물체는 항생제 저항성 캘러스로부터 재분화되었고 식물체 재분화효율은 약 27%이었다. 항생제에 저항성이 있는 캘러스에서 GUS 유전자가 발현되는 캘러스는 평균 35%였다. R0형질전환식물체는 성숙 개화하여 Rl 종자를 생성하였다. Rl 종자와 유모의 해부학적 GUS 활성을 분석하여 CaMV35S 프로모터 의해 GUS 유전자가 적절히 발현되는 것을 확인하였다. 또한 우리는 Rl세대에서 HPT유전자가 멘델 법칙에 따라 유전됨을 확인하였다