천문동 (Asparagus cochinchinesis (Lour.) Merr.)의 기내생장과 증식의 가능성을 검토하기 위하여 신초의 유기, 생장 및 발근에 적합한 배지, 식물생장조절제, 배양온도를 검정한 결과를 요약하면 다음과 같다. MS 기본배지에 3.0 mg/l BA 처리시 신초의 유기 및 생장이 가장 양호하였으며 MS 기본배지에 0.5 mg/l IBA 처리가 발근에 가장 효과적이었고 기내배양 온도는 23~25℃가 적합하였다.
An efficient plant regeneration system of Gentiana scabra through somatic embryogenesis was established. Leaves and roots of seedlings of Gentiana scabra excised after germination were cultured on MS basal medium with 2,4-D, NAA or BA. Embryogenic callus was obtained on MS medium with 0.5 mg/L 2,4-D alone or 0.1 mg/L 2,4-D combimation with 1.0 mg/L BA after 45 days of culture. These embryogenic calli gave rise to somatic embryos, which subsequently developed into plantlets on MS medium without PGRs. Also, shoots were effectively differentiated from embryogenic callus when root segments were cultured on MS medium supplement with 0.1 mg/L 2,4-D and 1.0 mg/L BA. Shoots were effectively rooted on MS medium without PGRs. In vitro flowers were formed from plantlets cultured on MS medium with 5% sucrose after 60 days of culture.
유색 칼라 세 품종(Sunlight, Chiante, Pink Persuation)의 기내 급속증식체계를 확립코자 정단분 열조직을 배양함에 있어 callus, 신초 및 뿌리 분화에 미치는 식물생장조절물질의 효과와 sucrose가 기내 괴경 형성 및 비대에 미치는 효과를 조사하였다. 식물체는 캘러스를 통하거나 또는 치상체에서 직접 분화되는 두 경로로 형성되었으며 2.0 mg/L BA 단용 처리에서 Sunlight품종은 53.3% 캘러스를, Chiante 품종은 56.7% 직접 신초를 형성하였다. 2.0-3.0 mg/L BA 단용 처리는 품종별로 식물체재 분화 빈도가 20-70%로 차이가 있었으나 세 품종 모두 3.0 mg/L. BA 단용 처리에서 신초 분화가 양호하였다. 다아체 형성에 미치는 cytokinin의 효과는 Sunlight품종은 1.0 mg/L 2ip 처리로 16개체를, Chiante 품종은 5.0 mg/L BA를 처리로 14개체를, Pink Persuasion품종은 1.0 mg/L BA처리로 12개체를 형성하였다. NAA는 세품종 뿌리분화에 효과가 없었으며 Sunlight 와 Chiante 품종은 1.0 mg/L IAA에서, Pink Persuasion 품종은 2.0 mg/L IBA가 효과적이었다. 괴경형성에 미치는 sucrose는 Sunlight 품종은 90 g/L, Chiante 및 Pink Persuasion 품종은 70 g/L 가 괴경 형성 및 비대에 효과적이었다.
This study was carried out to investigate the best explant source and combination of media and growth regulators for the regeneration of multiple shoots in soybean (Glycine max. L. Merr.) cv. ‘Iksannamulkong’. Multiple shoots could well be directly induce
Epidermal growth factor (EGF) induces well-documented mitogenic and differentiating effects on murine and bovine preimplantation embryos. However, the effects of EGF on apoptosis and implantation-related gene expression in bovine embryos developing in vitro have not been evaluated. The objective of this study was to determine the effects of exogenous EGF in the presence and absence of BSA on the preimplantation development of bovine embryos. In addition, we measured cell number, apoptosis, and expression of apoptosis and implantation-related genes of the blastocysts that developed in these culture conditions. In vitro produced bovine embryos were randomly cultured in the same medium containing 0 or 10 ng/ml EGF in the presence and absence of 0.8% BSA. More 2-cell embryos developed into blastocysts at day 7 when BSA was present than when BSA was absent. The addition of 10 ng/ EGF into the medium did not significantly increase the developmental rate and the cell numbers per blastocyst. However, addition of EGF in the presence of 0.8% BSA significantly reduced the degree of apoptosis in the blastocysts (P<0.01). To investigate whether EGF modulates mRNA expression of apoptosis-related genes, mRNA was prepared from single blastocysts and each preparation was subjected to RT-PCR for Bcl-2 and Bax transcripts. EGF did not alter the relative abundance of Bax gene expression in the presence of BSA, but increase Bcl-2 (P<0.01) The relative abundance of Interferon tau expression was increased by EGF treatment in the presence of BSA. These results suggest that EGF and BSA synergistically enhance Bcl-2 and interferone tau gene expression, which may result in a net increase in viability in bovine embryos.
Embryonic stem (ES) cells proliferate extensively in the undifferentiated state and have the potential to differentiate into a variety of cell types in response to various environmental cues. The generation of functional dopaminergic neurons from ES cells is promising for cell replacement therapy to treat Parkinson's disease. We compared the in vitro differentiation potential of pluripotent human embryonic stem (hES, MB03) cells induced with basic fibroblast growth factor (bFGF) or retinoic acid (RA). Both types of treatment resulted in similar neural cell differentiation patterns at the terminal differentiation stage, specifically, 75% neurons and 11% glial cells. Additionally, treatment of hES cells with brain derived neurotrophic factor (BDNF) or transforming growth factor (TGF)- during the terminal differentiation stage led to significantly increased tyrosine hydroxylase (TH) expression, compared to control (P<0.05). In contrast, no effect was observed on the rate of mature or glutamic acid decarboxylase-positive neurons. Immunostaining and HPLC analyses revealed the higher levels of TH (20.3%) and dopamine in bFGF and TGF- treated hES cells than in RA or BDNF treated hES cells. The results indicate that TGF- may be successfully used in the bFGF induction protocol to yield higher numbers of functional dopaminergic neurons from hES cells.
Epidermal growth factor (EGF) induces well-documented mitegenic and differentiating effects on murine and bovine preimplantation embryos. However, the effects of EGF on apoptosis and implantation-related gene expression in bovine embryos developing in vitro have not been evaluated. The objective of this study was to determine the effects of exogenous EGF in the presence and absence of BSA on the preimplantation development of bovine embryos. In addition, we measured cell number, apoptosis, and expression of apoptosis and implantation-related genes of the blastocysts that developed in these culture conditions. In vitro produced bovine embryos were randomly cultured in the same medium containing 0 or 10 ng/ EGF in the presence and absence of 0.8% BSA. More 2-cell embryos developed into blastocysts at day 7 when BSA was present than when BSA was absent. The addition of 10 ng/ EGF into the medium did not significantly increase the developmental rate and the cell numbers per blastocyst. However, addition of EGF in the presence of 0.8% BSA significantly reduced the degree of apoptosis in the blastocysts (P< 0.01). To investigate whether EGF modulates mRNA expression of apoptosis-related genes, mRNA was prepared from single blastocysts and each preparation was subjected to RT-PCR for Bcl-2 and Bax transcripts. EGF did not alter the relative abundance of Bax gene expression in the presence of BSA, but increase Bcl-2 (P < 0.01). The relative abundance of Interferon tau expression was increased by EGF treatment in the presence of BSA. These results suggest that EGF and BSA synergistically enhance Bcl-2 and interferone tau gene expression, which may result in a net increase in viability in bovine embryos.
In vitro culture of panicle has been the method to accumulate starch and protein in immature grains by providing nutrients after florets crossed between remote genotypes artificially. Grain filling means embryo development and sucrose translocation from photosynthetic source, and starch manufacture in endosperm. The concentrations of sucrose used to culture immature rice panicle were 5, 10, 15, 20% and glutamine was 20 mM. When immature rice panicles at 5 days after flowering were cultured in distilled water with different concentrations of sucrose, glutamine 20 mM and MS medium with different concentrations of sucrose, glutamine 20 mM for 30 days the later was effective on grain filling. The optimal concentration of sucrose on grain filling in vitro culture of rice panicle was 10% and the weight of grain cultured was 10.14 mg that was corresponded to 57% of intact plant. In the method of treating plant growth regulators, the culture of immature rice panicle adding in MS medium with Kinetin, IAA, ~textrmGA3 were effective on grain filling than the culturing of immature rice panicle after submerging in solutions of Kinetin, IAA, ~textrmGA3 for 1day. When immature rice panicle was cultured in MS medium with sucrose 10% and Kinetin 46.47 ~mu M it was effective on grain filling, respectively. The weight of grain cultured was 13.1mg that was corresponded to 75% of intact and germination rate was 51 %. When immature rice panicles were cultured in medium with different concentrations combined with Kinetin 4.65, 46.47, 464.7 ~mu~textrmM , IAA 5.71, 57.08, 570.80 ~mu~textrmM for 30 days and in medium with IAA 5.71, 57.08, 570.80 ~mu~textrmM for 15 days after culturing in medium with Kinetin 4.65, 46.47, 464.70 ~mu~textrmM for 15 days the effect on grain filling was similar.
마산약(山藥) 경절편(莖節片)의 기내조직(器內組織) 배양(培養)을 위해서 적정배지(適正培地)가 선발(選拔)됨에 따라 이에 적합시(適合時) 되는 생장조절물질(生長調節物質) 활성탄(活性炭)의 처리농도(處理濃度)를 구명(究明)함으로서 기내조직(器內組織) 배양(培養)에 의(依)한 증식율(增殖率)를 높이코져 무기강기성(無機강基性)이 낮은 1/8MS, White에 IAA와 NAA를 1~4mg / l 로 하고 활성탄(活性炭)을 0, 1, 3, 6g / l 수준(水準)으로 실험(實驗)을 실시(實施)하였던 바 다음과 같은 결과(結果)를 얻었다. 1. 1/8MS 배지(培地)의 경우 1~4mg / l, Kinetin 2mg / l 그리고 활성탄(活性炭)을 1~3g / l 첨가(添加) 하므로서 Shoot 유기(誘起)와 식물체(植物體)의 재분화률(再分化率)이 모두 100%에 달하는 효과(效果)를 보였으며 이러한 효과(效果)는 NAA처리시(處理時)에도 같은 경향(傾向)이 있었다. 2. White 배지(培地)의 경우 IAA 1mg / l, Kinetin 2mg / l 그리고 활성탄(活性炭) 6g / l 첨가처리(添加處理)와 NAA 4mg / l, Kinetin 2mg / l 그리고 활성탄(活性炭)을 1g / l 첨가처리(添加處理) 만이 식물체(植物體)의 재분화율(再分化率)이 l00%에 달하였으나 그 외(外) 처리(處理)에서는 대부분(大部分) 저조(低調)하였다. 3. 발육상태(發育狀態)를 보면 1/8M /S 배지(培地)의 경우 IAA 2mg / l, Kinetin 2mg / l 그리고 활성탄(活性炭)을 1g / l 첨가처리(添油處理)와 NAA 4mg / l, Kinetin 2mg / l 활성탄(活性炭)을 1g / l 첨가처리(添加處理) 하므로서 모두 주당(株當) 본수(本數)가 2.3~2.7개(個)이고 발육상태(發育狀態)도 활성탄(活性炭)0g / l, 3g / l, 6g / l 처리(處理)보다 양호(良好)하였다. 4. 그러나 White 배지(培地)의 경우 IAA 1~4mg / l, NAA 1~mg / l 그리고 Kinetin 2mg / l 처리(處理)의 대부분(大部分)이 주당(株當) 본수(本數)가 거의 1개체(個體) 정도(程度)이도 발육상태(發育狀態)도 불량(不良)하였으나 NAA 4mg / l Kinetin 2mg / l 그리고 활성탄(活性炭) 1g / l 첨가처리(添加處理)에서 만이 주당(株當) 본수(本數)가 2.3개이고 개체당(個體當) 발근수(發根數)가 월등(越等)히 많았다. 5. 실험결과(實驗結果) 마 경절편(莖節片) 배양(培養)의 Shoot유가(誘起)에 가장 효과적(效果的)인 배지(培地)는 1/8MS+1AA 2mg / l+Kinetin 2mg / l+활성탄(活性炭) 1g / l 이였으며, White+NAA 4mg / l+Kinetin 2mg / l+활성탄(活性炭)1g / l 로 처리(處理)하는 것이 바람직한 결과(結果)를 얻었다.
The study was conducted to determine the Ms orthogonaL modia and the concentration of plant growth regulator for seed matura-tion and growth of rhizome from Cymbidium goeringii Germination waswell in dark condition, but the growth of rhizome was better un-der dark than under light condition in MS orthoTonal . Sucrose con-centration( 3 %) gave better results than higher ones(6%), andthe use of NAA(0.1 PPm) effect significant difference of seed ge-rmination .But the growth of rhizome was best in medium Containingsucrose concentration(3%) Ippm NAA and 1 PPm BA.
우리나라에서 고구마 장려품종인 홍미와 신미를 액아배양시 explant의 크기 NAA, BA 및 kinetin의 농도가 기관분화와 생육에 미치는 영향을 구명하고저 본 실험을 실시하였으며 실험결과를 요약하면 다음과 같다. 1. 5mm되는 explant 배양이 2mm explant 배양보다 기관분화 및 생육이 좋았으며 홍미는 MS 배양에 NAA 0.1mg/ 와 kinetin 1mg/ 을 조합처리할 때 신미는 MS배지에 NAA 0.1mg/ 와 kinetin 1mg/ 을 조합처리할 때와 kinetin 1mg/ , BA 0.1mg/ 을 단독처리할 때 shoot의 분화가 좋았다. 2. 뿌리분화는 홍미와 신미가 비슷한 결과를 보였으며 NAA 0.lmg/ 와 kinetin 1mg/ 을 조합처이한 배지에서 뿌리수와 뿌리길이가 증가하였다. 3. BA의 농도가 증가함에 따라 비정상 식물체의 출현이 많았으며 한 개의 explant에서 여러개의 shoot의 길이가 짧았다. 4. 이차계대배양에서 shoot의 분화 및 생장은 NAA 0.1mg/ 와 kinetin 1mg/ 가 첨가된 배지에서 좋은 결과를 보였고 뿌리의 분화는 0.1 mg/ BA에 첨가된 배지에서 가장 효과적이었다.