• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2018년도 추계학술대회
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• pp.80-80
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• 2018

Hosta is a genus of the family Asparagaceae and distributed in East Asia. There are six Hosta species (Hosta capitata (Koidz.) Nakai, H. clausa Nakai, H. jonesii M.G.Chung, H. minor (Baker) Nakai, H. venusta F.Maek., and H. yingeri S.B.Jones) native to Korea and among them, four species (H. minor, H. jonesii, H. venusta and H. yingeri) are endemic to the Korea peninsula. Hosta is generally propagated by seed, crown division or tissue culture. However, tissue culture is a more efficient method to mass proliferation, a new cultivar development and disease-free plantlet production in a limit time. Hence, we conducted this study to evaluate the influence of various plant growth regulators (PGRs) treatments on the induction of callus and somatic embryo of the six Hosta species. Leaf, petiole and root were used to select optimum tissue culture explants. Petiole explants thus only were used for callus induction and somatic embryogenesis with TDZ (0.1, 0.5 or 1.0mg/L) and NAA (0.1 or 0.5 mg/L) combinations. After 12 weeks of culture, the highest rate of somatic embryogenesis was achieved on modificated MS medium containing 1.0 mg/L TDZ and 0.1 mg/L NAA in H. capitata and H. minor (15.5%, respectively), 0.1 or 0.5 mg/L TDZ and 0.1 mg/L NAA in H. jonesii (22.2%), 1.0 mg/L TDZ and 0.5 mg/L NAA in H. yingeri (26.7%), and 0.1 mg/L TDZ and 0.5 mg/L NAA in H. venusta (53.3%). H. clausa showed very low effect on somatic embryogenesis by PGRs; 2.2%. There was interspecies difference to PGRs respond for callus and somatic embryo induction. Regenerated multiple shoots and plantlet of H. minor, H. jonesii, H. venusta and H. yingeri were obtained via somatic embryogenesis.

• 한국환경농학회지
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• 제20권2호
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• pp.116-121
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• 2001

저선량 ${\gamma}$선 조사가 기내 유기한 감자 소괴경에서 생산한 "대지 (Solanum tuberosum L. cv. Dejima)" 품종 씨감자의 맹아발생과 포장에서의 생육과 수량 및 생리활성에 미치는 효과 등을 알아보고자 저온 저장한 감자 괴경에 ${\gamma}$선을 $0.5{\sim}30$ Gy 까지 조사하여 수행한 결과는 다음과 같다. 저선량 ${\gamma}$선 조사한 감자 괴경의 맹아 출현율은 저장 기간에 관계없이 대체로 1 Gy와 2 Gy 조사구에서 높았고 맹아 길이는 2 Gy와 4 Gy 조사구에서 유의성있는 증가효과를 보였으며 맹아수에서는 15일 저장구의 4, 8, 16 Gy 조사구에서 유의성있는 증가효과를 보였다. 포장생육에서는 45일 저장구가 모든 선량에서 유의성있는 생육 및 수량 증가효과를 보였는데 특히 4 Gy 조사구에서 뚜렷한 증가효과를 보였다. 항산화효소 활성은 저선량 조사와 생육에 따라 어떠한 경향을 보이지 않았으나 catalase는 모든 저선량 조사구가 대조구에 비해 낮았고, peroxidase는 생육이 양호하였던 45일 저장구의 4 Gy 조사구에서 증가하였다.

• Journal of Plant Biotechnology
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• 제40권3호
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• pp.141-146
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• 2013

본 연구는 낙엽송 배발생세포의 배양기간에 따른 현탁세포의 생장, 체세포배 유도 및 발아를 위한 다양한 삼투압제 종류 및 농도 효과를 조사하기 위해 수행되었다. 배발생 현탁세포의 생장은 배양일수가 증가함에 따라 settled cells volume (SCV)가 지속적으로 증가하는 경향을 보여 배양 18일 경에는 최대 10.1 ml의 SCV를 보였고, 그 이후로는 세포생장이 감소하였다. 현탁세포로부터 체세포배 발생을 위한 삼투압제 종류 및 농도에 따른 효과 비교에서 최대의 체세포배 유도 수는 0.2 M sucrose 처리구에서 352.3개(/g FW)로 나타났으며, 0.2 M maltose (203.7) 및 0.3 M maltose (193.7) 처리구에서 또한 효과가 있었다. 그러나 7.5% polyethylene glycol (PEG)이 첨가된 0.15 M sucrose 혹은 maltose 각각의 처리구에서는 체세포배 발생이 전혀 이루어지지 않았다. 다양한 삼투압제 종류 및 농도에서 발생된 체세포배의 발아율 비교에서는 최대 자엽 형성율(25.2%) 0.3 M maltose, 하배축 형성률(39%), 뿌리 발생율(30.3%) 및 식물체 재분화율(3.5%)은 0.2 M sucrose 처리구에서 각각 나타났다.

• 한국환경농학회지
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• 제29권4호
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• pp.374-380
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• 2010

본 연구에서는 농촌진흥청에서 개발한 LED Chamber System을 이용하여 명기시간 동안 광질과 광조사 방법 제어가 단절단엽의 국화 배양소식물체(Dendranthema grandiflorum L., cv. 'Cheonsu')의 생장에 미치는 영향을 검토하였다. 실험은 청색, 적색 및 녹색의 단일광질 또는 청색+적색, 청색+녹색 및 적색+녹색의 혼합광질 조건하에서 이들 광질을 명기 16시간 동안 연속적으로 또는 초당 50회 간격과 분당 20초간격으로 간헐적으로 제어하면서 42일간 수행하였다. 총 일장을 4시간 단축한 분당 20초 간격의 간헐조사는 관행의 형광등 연속조사에 비해 국화의 절간길이 신장에 의한 신초신장을 촉진하였으나, 배양소식물체의 양적생장은 연속광 처리에 의해 유의하게 증가하였다. 한편, 명기동안 녹색광을 초당 50회 간격으로 간헐제어한 경우 연속조사에 비해 건물중이나 엽면적 증대와 같은 양적생장은 억제되었으나 형태적인 면에서의 절간신장은 촉진되었다. 따라서, LED Chamber System을 이용한 광질이나 광조사 방법의 제어는 관행의 형광등 이용 연속조사에 비해 명기시간 단축에 의한 전력소모량 감소 및 기내 배양소식물체의 생장이나 형태제어에 효과적인 배양기술로 이용 가능할 것으로 판단된다.

• 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.

• Molecules and Cells
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• 제23권3호
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• pp.323-330
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• 2007

The mature wheat embryo is arguably one of the best explants for genetic transformation because of its unlimited availability and lack of growth season restriction. However, an efficient regeneration system using mature wheat embryos (Triticum aestivum L.) is still not available. To identify genes related to the tissue culture response (TCR) of wheat, QTLs for callus induction from mature embryos and callus regeneration were mapped using an RIL population derived from the cross of 'Wangshuibai' with 'Nanda2419', which has a good TCR. By whole genome scanning we identified five, four and four chromosome regions conditioning, respectively, percent embryos forming a callus (PEFC), percent calli regenerating plantlets (PCRP), and number of plantlets per regenerating callus (NPRC). The major QTLs QPefc.nau-2A and QPcrp.nau-2A were mapped to the long arm of chromosome 2A, explaining up to 22.8% and 17.6% of the respective phenotypic variance. Moreover, two major QTLs for NPRC were detected on chromosomes 2D and 5D; these together explained 51.6% of the phenotypic variance. We found that chromosomes 2A, 2D, 5A, 5B and 5D were associated via different intervals with at least two of the three TCR indexes used. Based on this study and other reports, the TCRs of different explant types of wheat may be under the control of shared or tightly linked genes, while different genes or gene combinations may govern the stages from callus induction to plantlet regeneration. The importance of group 2 and 5 chromosomes in controlling the TCRs of Triticeae crops and the likely conservation of the corresponding genes in cereals are discussed.

• 한국산림과학회지
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• 제79권2호
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• pp.109-114
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• 1990

피나무의 조직배양(組織培養)에 의(依)한 대량증식(大量增殖) 방법(方法)을 확립(確立)하기 위하여, 15년생(年生) 성숙목(成熟木)의 액아(腋芽)를 IS, MS 및 WPM배지(培地)에 배양(培養)하였다. 5수절(水凖)의 BAP농도(濃度)가 검정(檢定)되어, IS와 WPM배지(培地)에서는 BAP 1.0mg/l 첨가(添加)가 줄기 형성(形成)과 생장(生長)을 촉진(促進)한 반면(反面), MS배지(培地)에서는 BP 0.5mg/l 첨가(添加)가 효과적(效果的)이었다. 최적조건(最適條件)은 BAP 1.0mg/l 첨가(添加)의 WPM과 0.5mg/l 첨가(添加)의 MS배지(培地)이었다. 형성(形成)된 줄기는 다경유도(多莖誘導)를 위하여 BAP 0.2mg/l 첨가(添加) 배지(培地)에 다식(多植)하여, 한달안에 약(約) 2배(倍)로 증식(增殖)되었다. 발근(發根)은 고농도(高濃度)의 IBA에서 촉진(促進)되어, IBA 3.0mg/l 첨가(添加)의 1/2MS에서 83.3%의 발근율(發根率)을 얻었다. 재분화(再分化)된 유치물체(幼植物體)는 환경순화(環境馴化)될 수 있었다. 액아배양(腋芽培養)에 의(依)한 줄기 형성(形成)과 생장면(生長面)에서 클론간(間) 변이(變異)를 조사(調査)하기 위하여 수형목(秀型木) 7클론이 검정(檢定)되었다. 조직배양능력(組織培養能力)에 있어서 수형목(秀型木) 클론간(間) 변이(變異)는 Duncan의 다중검정(多重檢定) 5% 유의수준(有意水準)에서 유의성(有意性)이 인정(認定)되었으며, 강원(江原) 12호(號)가 BAP 1.0mg/l 첨가(添加) WPM에서 가장 좋은 반응(反應)을 나타냈다.

• Plant Biotechnology Reports
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• 제2권3호
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• pp.179-189
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• 2008

We established an efficient plant regeneration system for Catharanthus roseus L. (G.) Don through somatic embryogenesis. Embryogenic callus was induced from hypocotyl of seed germinated in vitro. Somatic embryogenesis in Catharanthus has been categorized into three distinct stages: (1) initiation and proliferation of embryo; (2) maturation, and; (3) germination or plantlet conversion. Beside plant growth regulators, various stages of embryogenesis were screened for their response to a wide variety of factors (pH, gelrite, light, sugar alcohols, polyethyleneglycol and amino acids), which affect embryogenesis. All of the tested factors had a small to marked influence on embryogeny and eventual conversion to plantlets. The plantlets were acclimatized successfully in a greenhouse. To our knowledge, this is the first report describing a detailed study of various cultural factors which regulate embryogenesis in C. roseus. The results discussed in this paper may be used in mass propagation to produce medicinal raw material, and the embryo precursor cells could be used in genetic modification programmes that aim to improve the alkaloid yield as well.

• 한국한의학연구원논문집
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• 제14권1호
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• pp.113-116
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• 2008

Petiole explant of Glehnia littoralis Fr. Schmidt was in vitro cultured MS plant medium(DUCHEFA co.) supplemented with various plant growth regulators and examined to find out their optimum combination and concentration for plantlet regeneration. We investigated optimal condition for efficient plant regeneration through adventitious shoot formation on MS plant medium with various kinds of plant growth regulators. Embryogenic calli and adventitious shoot formation were greatly influenced by plant growth regulators. Embryogenic calli induction showed a good response on MS medium supplemented with NAA and BA than others. Especially, combination of 1.0 mg/L NAA and 0.5 mg/L BA on MS medium led to the greatest frequency in adventitious shoot. The results suggest that plant regulator selection be important factor to achieve an efficient regeneration.

• Journal of Plant Biotechnology
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• 제8권1호
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• pp.27-35
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• 2006

Plantlet regeneration in Asteracantha longifolia(L.) Nees (Acanthaceae), a medicinal herb has been achieved from seedling explants on basal MS medium. Three different seedling explants including node, internode and leaf segments on used. Of these three explant, leaf explants gave better response for both callus mediated organogenesis and direct multiple shoot induction. Number of explants showing differentiation of shout buds was higher on MS media supplemented with BA compared to kinetin. MS medium fortified with BA ($2.0mgl^{-1}$) and NAA ($0.5mgl^{-1}$) was found to be most suitable for both callus mediated organogenesis and elongation of shouts. The elongated shoots were successfully routed on MS medium fortified with NAA or IBA. Among them $0.1mgl^{-1}$ NAA or $0.2mgl^{-1}$ IBA provides better response for rhizogenesis. Regenerated plantlets were successfully established in soil where 85.4% or them developed into morphologically normal and fertile plants. RAPD profiling using four decamer primers confirmed the genetic uniformity of the regenerated plantlets and substantiated the efficacy and suitability of this protocol for in vitro propagation of A. longifolia.