• 한국축산식품학회지
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• 제32권4호
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• pp.389-395
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• 2012

Cloned animals are a result of asexual reproduction of animals using somatic cell nuclear transfer. Ever since the first report of a cloned sheep 'Dolly' produced by SCNT, increasing numbers of livestock, such as bovine and swine clones, have been generated worldwide. Foods derived from cloned animals have not been produced yet. However, the food safety of cloned animals has provoked controversy. The EU Food Safety Authority and U.S. Food and Drug Administration announced that milk and meat from cloned and non-cloned animals have no difference regarding food safety. However, food derived from cloned animals is considered unsuitable for eating vaguely. Moreover, there were scant information about cloned animals in Korea. Therefore, we surveyed the number of cloned animals worldwide including Korea and summarized the reports for cloned animals and discussed predictable problems.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2003년도 심포지엄
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• pp.50-58
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• 2003

Isolation and culture of leaf protoplasts from two chilli cultivars (Capsicum annuum var. accumnatum and Bird chilli) were developed to enhance selection process in the somatic hybridization programmes. In order to isolate the protoplasts from leaves of these two chilli cultivars different incubation periods (3, 5 and 10 hours) were tested with combinations of enzyme mixtures containing cellulase and macerozyme. Leaves were incubated on three enzyme mixtures (2% cellulase + 0.4% macerozyme, 1% cellulase + 0.2% macerozyme and 0.5% cellulase + 0.1 % macerozyme in 13% mannitol) at 251oC in the dark. Three hours of incubation using 2% cellulase and 0.4% macerozyme was the best for the protoplast isolation of both chilli cultivars tested. The yield was 5 ${\times}$ 108protoplasts/ml/ g leaf tissue in both chilli varieties. It was found that in the mixed nurse method using Nagata and Takebe (NT) medium supplemented with 1.0mg/12,4-D, NAA and BAP with 0.5M mannitol and 1.2% Sea Plaque agarose is the best medium for protoplast culture. Protoplasts of Capsicum annum var. accumnatum were alive for 14 days forming cell walls and initiating cell division.

• Journal of Plant Biotechnology
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• 제46권2호
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• pp.79-87
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• 2019

One of wild diploid Solanum species, Solanum chacoense, is one of the excellent resources for potato breeding because it is resistant to several important pathogens, but the species is not sexually compatible with potato (S. tuberosum) causing the limitation of sexual hybridization between S. tuberosum and S. chacoense. Therefore, diverse traits regarding resistance from the species can be introgressed into potato via somatic hybridization. After cell fusion, the identification of fusion products is crucial with molecular markers. In this study, S. chacoense specific markers were developed by comparing the chloroplast genome (cpDNA) sequence of S. chacoense obtained by NGS (next-generation sequencing) technology with those of five other Solanum species. A full length of the cpDNA sequence is 155,532 bp and its structure is similar to other Solanum species. Phylogenetic analysis resulted that S. chacoense is most closely located with S. commersonii. Sequence alignment with cpDNA sequences of six other Solanum species identified two InDels and 37 SNPs specific sequences in S. chacoense. Based on these InDels and SNPs regions, four markers for distingushing S. chacoense from other Solanum species were developed. These results obtained in this research could help breeders select breeding lines and facilitate breeding using S. chacoense in potato breeding.

• Plant Resources
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• 제5권1호
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• pp.29-44
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• 2002

In this study, plant regeneration through in vitro culture from plantlet stems of Yooja (C. junos Sieb.) and trifoliate orange (P. trifoliata Rafin.) was attempted to make mass-production system of virus-free plants having the same genotype with mother plant. In order to investigate physiological change depending on the developmental stage of plant regeneration, the changes of total protein, peroxidase and esterase activity and their isozyme patterns as well were examined in 1/2 MS medium. The results are as follows : 1. The MS medium for the optimal callus induction and shoot formation was utilized. The medium was supplemented either with 2,4-D and Kinetin or with BA and NAA. The optimal concentrations were the combination of 1.0mg/ 2,4-D +0.3mg/ Kinetin and 1.0mg BA +0.3mg NAA in callus induction and shoot formation, respectively. 2. For the plant regeneration from somatic embryos, 1/2 MS medium was used with supplements of growth regulators (free, 1.0mg/ IBA +1.0mg/ BA ,0.5mg/ IBA +0.5mg/ BA). Shooting and rooting were the best in the treatment of 0.5mg/ IBA and 0.5mg/ BA combination. 3. The total protein content has a tendency of increase with the developmental stage of embryo, but it was decreased at the plantlet. Also it was the highest at 8 and 6 weeks stage in C. junos Sieb. and P. trioliata Rafin, respectively. In the SDS-PAGE pattern of protein, C. junos Sieb. showed bands of 29.0 and 40kDa at 10 weeks. The 45,66 and 97.4 kDa bands at 10 weeks of culture were shown in P. trifoliata Rafin. 4. The highest esterase activity was shown at the 6 and 8 weeks of culture in C.junos Sieb. and P. trifoliata Rafin.., respectively. 5. Esterase isozyme patterns were shown difference according to the developmental stage. In C. junos Sieb. a new band was observed at pl 7.7 following 4 weeks culture. On the other hand, new bands in P. trifoliata Rafin. were observed at pl 7.5~6.5 following 4 and 6 weeks culture, respectively.

• 식물분류학회지
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• 제43권2호
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• pp.139-145
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• 2013

국내에 자생하는 황기속(Astragalus L.) 식물인 정선황기(A. koraiensis)의 핵형을 분석하고, 5S 및 45S rDNA 유전자를 이용한 FISH 실험에 기초하여 세포유전학적 연구를 수행하였다. 핵형 분석 결과, 정선황기의 체세포 염색체수는 2n = 16으로, 기본 염색체수는 x = 8임을 확인하였다. 염색체 조성은 6쌍의 중부염색체(염색체 1, 3, 4, 5, 6, 8)와 2쌍의 차중부염색체(염색체 2, 7)로 구성되었다. 정선황기의 염색체상에서의 FISH 결과, 1쌍의 45S rDNA signal이 5번 염색체의 동원체 부위에서 관찰되었고, 2쌍의 5S rDNA signal이 4번 염색체의 단완 말단부위와 7번 염색체의 동원체 부위에서 관찰되었다. 이는 기존의 황기 및 제주황기, 몽골황기(A. mongholicus) 와는 전혀 다른 FISH 패턴을 보이고 있어 정선황기가 고유종임을 암시하지만, 형태학적으로 유사한 갯황기(A. sikokianus) 및 A. bhotanensis 와의 비교연구를 수행하여 정확한 분류학적 처리가 이루어져야 할 것이다.

• Journal of Plant Biotechnology
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• 제47권3호
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• pp.185-193
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• 2020

최근, 유전자교정 작물의 상업화 승인 건수가 급속하게 늘어나고 있으며, 국내에서도 유전자교정 작물의 개발에 대한 집중적인 투자를 통하여 국제경쟁력을 높이기 위하여 노력하고 있다. 그러나 기존의 유전자변형작물의 상업화 과정에서 끊임없이 제기되어온 인체 및 환경에 대한 잠재적인 위해성 논란이 유전자교정 작물에 대하여서도 제기되고 있다. 특히, 비의도적 돌연변이(off-target)가 가장 큰 논란의 중심이 되고 있다. 따라서 본 리뷰는 식물이 내포하고 있는 장점인 배수체, 체세포 돌연변이 그리고 자연 상태에서 아그로박테리아의 T-DNA 단편의 수평 전이로 창출된 자연적인 유전자변형작물과 기존에 상업화가 승인된 유전자변형작물 이벤트들의 게놈 내 비의도적 돌연변이 사례 등을 검토한 결과 유전자교정 작물에서 나타나는 대부분의 비의도적 돌연변이는 인체 및 환경에 미칠 수 있는 위해성을 우려할 만한 수준이 아니라고 할 수 있었다. 이에, 유전자교정 작물의 안전성 평가를 위하여 새로운 규정을 제정할 필요가 없으며 기존의 유전자변형작물의 안전 관리규정을 일부 "용어의 정의" 등만 개정하여 적용하면 충분할 것으로 사료 되었다.

• Journal of Dairy Science and Biotechnology
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• 제22권1호
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• pp.27-35
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• 2004

The shelf lift of market milk should be determined based on the flavor which is influenced by environmental and sanitary conditions of dairy farm, milk processing plant, and storage and transportation facility as well as compositional quality, such as protein and fat, of the milk itself. The legal shelf life of market milk is often limited by microbiological quality, e.g. total bacterial count, coliform count, and food poisoning bacteria. The bacteria involved with milk spoilage and poisoning are originated from bacteria contaminating milk after pasteurization or spores surviving the heat treatment of pasteurization. The important factors which influence the shelf life of market milk are microbiological quality of raw milk, pasteurization condition, post-pasteurization contamination, and temperature during storage and transportation. The organoleptic quality and shelf life of market milk should be further improved by satisfying the consumer's taste, which depends on somatic cell count and bacterial count of milk, feed quality, foreign substance in milk, and physical treatment during processing and transportation.

• 생약학회지
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• 제21권3호
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• pp.205-209
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• 1990

The study for the quantitative analysis of saikosaponin of Bupleurum falcatum root produced by tissue culture was attempted. The optimal concentration of 2,4-D was 0.1 mg/l for inducing the callus. The induction and growth of the adventitious root from the callus was obtained in the suspension culture containing MS basal medium supplemented with no plant growth regulators. The results of the quantitative analysis of saikosaponins by high performance liquid chromatography (HPLC) showed that the content of saikosaponin a and c was high in the one-year-old root from somatic embryos and that of saikosaponin d was remarkably high in three-months-old adventitious root from callus.

• 한국약용작물학회지
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• 제22권1호
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• pp.1-7
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• 2014

Codonopsis lanceolata (Campanulaceae) has been used in traditional medicines, as its roots contain several kinds of 3,28-bidesmosidic triterpenoid saponin with high medicinal values. In this study, we induced hairy root-derived transgenic plants of C. lanceolata and analyzed triterpenoid saponins from the leaf, stem and root. Transgenic plants were regenerated from the hairy roots via somatic embryogenesis. The saponins are lancemaside A, B and E, foetidissimoside A, and aster saponin Hb. Transgenic plants contained richer triterpenoids saponin than wild-type plants. Major saponin lancemaside A was the most abundant saponin in the stem from transgenic-plant, $4.76mg{\cdot}1^{-1}dry$ stem. These results suggest that transgenic plants of C. lanceolata could be used as medicinal materials for the production of triterpene saponins.

• 식물분류학회지
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• 제33권3호
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• pp.279-293
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• 2003

한국산 대극속(Euphorbia L.) 13종의 체세포염색체의 분류학적 가치를 평가하기 위하여 본 연구를 수행하였다. 본 연구에 취급된 분류군들의 체세포염색체수는 2n= 12, 20, 22, 28, 40, 42, 56이었고, 기본염색체수는 x=6, 7, 10, 11이었다. 본 연구에서 체세포염색체수가 처음으로 밝혀진 분류군은 낭독(E. pallasii Turcz.; 2n=20), 단주낭독(E. hylonoma Hand.-Mazz; 2n=20.), 두메대극(E. fauriei H. L$\acute{e}$v. & Vaniot ex H. L$\acute{e}$v.;2n=28), 암대극(E. jolkini Boiss.; 2n=28)의 4종류이었으며, 기존의 보고와 일치하는 분류군은 개감수(E. sieboldiana Moor. & Decne.; 2n=20), 붉은대극(E. ebracteolata Hayata; 2n=20), 땅빈대(E. humifusa Willd. ex Schlecht.; 2n=22)의 3종류이었다. 반면 기존의 보고와 다르게 나타난 종류는 흰대극(E. esula L.; 2n= 16, 20, 60, 64 vs 2n=20), 등대풀(E. helioscopia L.; 2n=12, 42 vs 2n=42), 참대극(E. lucorum Rupr.; 2n=28, 40 vs 2n=56), 대극(E. pekinensis Rupr. in Maxim.; 2n=24 vs 2n=28, 56), 큰땅빈대(E. maculata L.; 2n=28, 42 vs 2n=12), 애기땅빈대(E. supina Raf.; n=7 vs 2n=40)이었다. 낭독, 붉은대극, 단주대극은 염색체의 수와 크기 및 부수체의 존재에 의해 다른 분류군들과 뚜렷히 구분되었으며, 큰땅빈대, 땅빈대, 애기땅빈대는 외부형태, 해부, 화분학적 형질의 공통성에도 불구하고 기본염색체수 및 체세포염색체수에서 차이를 보였다. 체세포염색체에서 얻어진 결과는 Webster(1967)의 분류체계보다 Ma and Hu(1992)의 분류체계가 타당한 것으로 판단되었다. 이와 같이 본 연구에서 얻어진 체세포염색체에 관한 형질은 절 수준에서 분류학적으로 유용하게 적용되었으며, 일부 종의 유연관계를 파악하는데 그 유용성이 인정되었다.