Proceedings of the Plant Resources Society of Korea Conference
/
1999.10a
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pp.46-57
/
1999
Ginseng(Panax ginseng C.A. Meyer) is important medicinal plant but requires 4-year cultivation for root harvest because of slow growth. In contrast, ginseng callus and hairy roots grow vigorously and may Produce the same or more biologically active compounds for human health than natural ginseng roots. Therefore, ginseng callus and hairy roots can be used for commercial purposes. Polyacetylene, one of anti-cancer compounds in ginseng, was not detected in the callus cultured on the medium containing 2, 4-B, but cells derived from the callus growth was excellent, The ginseng calli cultured on the medium containing 2mg11 CPA and 0.05mg/1 BA was grown vigorously and produced panaxydol, one of ginseng polyacetylene. The biosynthesis of polyacetylene in callus was not affected by addition of NAA and sucrose in media. The SH medium was better than the MS medium for ginseng callus growth and biosynthesis of panaxydol. Another ginseng anti-cancer compounds, ginsenoside-Rg$_3$, Rh$_1$and Rh$_2$ were detected in ginseng hairy roots by heat treatment. Those of Panax ginseng were obtained after root disks of three-year old roots were infected with Agrobacterium rhizogenes Rl000 $A_4$T in dark condition after one month of culture. The optimum growth of hairy roots was achieved in the culture of 1/2 MS liquid medium in dark(22$^{\circ}C$) under 60 rpm gyratory shaking. Hairy roots grew well in 5 ι Erlenmeyer flasks, 1ι roller drums, 10ι jar-fermenters, and especially in 20ι air-lift .culture vessels. All heat treatments had remarkably different ginsenoside contents. Eleven ginsenosides were determined in heat treatment, eight in freeze dried hairy roots. Contents of ginsenoside-Rbl , Rb2, Rc, Rd. Re, Rf, and Rg$_1$tested in all heat treatments were less than those of freeze dried hairy roots. Contents of glnsenoside-Rg$_2$ in heat treatment for 1 hour at 105$^{\circ}C$ was 4.92mg/g dry wt, 3.9 times higher than 1.27 mg/g dry wt of freeze dried hairy roots. The optimum condition of heat treatment for the production of ginsenoside-Rg$_3$and Rhl was 2 hours at 105$^{\circ}C$, and ginsenoside content was 2.58mg/g dry wt and 3.62mg/g dry wt, respectively. The production of ginsenoside-Rh2 was the highest in heat treatment for 2 hours at 105$^{\circ}C$ among treatments examined, and ginsenoside-Rh$_2$content was 1.08mg/g dry wt.
Ko, Kyeong-Min;Yang, Deok-Chun;Park, Ji-Chang;Choi, Kang-Ju;Choi, Kwang-Tae;Hwang, Baik
Journal of Plant Biology
/
v.39
no.1
/
pp.63-69
/
1996
A hairy root clone of Panax ginseng C.A. Meyer, HRB-15 was cultured iu various conditions with 3 L bubble type bioreactor to enhance both growth and ginsenoside production. The hairy roots were more rapidly grown under the dark condition than under the light condition. However, total amount of ginsenoside of hairy roots cultured under the light for 30 days increased 2 folds as compared with the dark condition and was 1.10% based on 6 ginsenosides. Especially, ginsenoside-Re was significantly increased and some ginsenosides except for ginsenoside-Re was slightly reduced. Also, the growth of hairy roots decreased about 30% as compared with the dark condition. In contrast, addition of sodium acetate led to decreased production of ginsenoside and growth of hairy roots under light condition. The influence of potassium dihydrogenphosphate concentration was examined in MS medium and a 1.25 mM concentration was found to be the most appropriate for growth and ginsenoside production under light condition. Two-step process of hairy roots culture with yeast elicitation or without ammonia in culture medium was developed to enhance growth and giusenoside synthesis. $50\;\mu\textrm{g}$ of yeast elicitor per g of fresh weight showed a synergistic effect on the ginsenoside synthesis of hairy roots on 20 days after culture. At that time, the content of total ginsenoside was 1.15%, while the growth of hairy roots decreased 21 % as compared with the dark condition. In addition, when elimination of ammonia on 20 days after culture, the content of total ginsenoside was 1.26% with significant increment of ginsenoside-Rd (0.27%) in addition to ginsenoside-Re and the growth of hairy roots decreased 10% as compared with the dark condition. In this system, we have demonstrated a unique two-step process of hairy root cultures to maximize biomass and secondary metabolites. It has found possibility to enhance ginsenosides production by growing hairy roots in this method.
To investigate the effects of C. E. P. A(2-chloroethyl phosphonic acid) on the ripening of tobacco leaf, the effects on the yield and quality of leaf tobacco, this experiments were carried out during the period of from 1970 to 1971 at tobacco experiment station, Sosa, Korea and 3 locations. The results are summarized as follows. 1. The higher the C. E. P. A concentration was, the more the leaf ripening was accelerated. During the period from 3 to 4 days after treatment, the differences of leaf ripening among levels were prominent. 2. Treatment with C. E. P. A only on the upper surface of the tobacco leaf, accelerated the ripening of that particular part treated, but not apparently the other parts of leaf. 3. Distinctive acceleration of leaf ripening was, obserbed in the fully develope1lower leans, however, the upper leaves were indistinctive. 4. The higher C. E. P. A concentration was, the more the effect of ripening acceleration was. But the yield was reduced over 900ppm because of the low of growth of leaves and the reduced yield was 90% at the 3, 000ppm. So the proper concentration was regarded as 900ppm. 5. In the view point of the days of C. E. P. A ripening acceleration, it was shortened one days at 100 ppm, three days at 300ppm, three days at 450ppm, four days at 900ppm, seven days at 3, 000ppm. 6. In the point of curing process, it was possible that the curing time and fuel was reduced 29% and 45% respectively in the C. E. P. A treatment than the check. 7. Therefore, if it is treated the C. E. P. A at 900ppm in the tobacco cultivation, the quality shall be increased 13.5% and the price shall be increased 12% in the 10 Are. In the point of subsidiary affect, it is possible that the C. E. P. A ripening acceleration is shortened about 7 days at 3, 00ppm and curing time is shortened about 24 hours.
1. Chemical components of fresh tobacco leaves at topping stages were affected variously by fertilizer application level. The more fertilizers were applicated, the higher nitrogen content of leaves was shown regardless of the soil fertility, but phosphorus content was not affected either by phosphorus rate or soil fertility. Potassium content was higher in the leaves grown in fertile soil than infertile at the same application rate. 2. Maturation of tobacco leaves was delayed by applying high level of nitrogen fertilizer, especially in fertile soil. The excessive accumulation of nitrogen in tobacco leaves at later stage of growth resulted in poor quality index for the high content of nicotine and low content of reducing sugar in cured leaves. 3. Nicotine content of cured leaf was increased significantly as nitrogen content increased, regardless of soil fertility, but reducing sugar content was reduced. Nicotine and reducing sugar content of cured leaf were higher in fertile than in infertile soil. 4. Resulting from the facts that nicotine contents were negatively correlated and reducing sugar contents were positively correlated with grading value (Won/Kg), authors suggested that grading index (Won/Kg) of the Office of Monopoly be based on quality index from chemical components of cured leaves.
Kim, Jae-Hyun;Park, Yong-Hack;Chung, Youl-Young;Kim, Kwang-Chul;Shin, Seung-Gu;Kuem, Wan-Soo
Journal of the Korean Society of Tobacco Science
/
v.31
no.2
/
pp.69-74
/
2009
Potato Virus Y (PVY), PVY-vein necrosis strain, causes severe damage at growth, yield and leaf quality on flue-cured tobacco in Korea. The development of PVY resistant flue-cured varieties without quality deterioration is therefore urgently desired. The flue-cured tobacco, KF120 (Korea Flue-cured 120), was a male-sterile (ms) $F_1$ hybrid derived from the cross between msKF117 and KF0007-7. msKF117 was developed from the cross of NC82 with N. africana and KF0007-7 was developed from the cross of KF117 with NC82. The agronomic characteristics and disease resistance of KF120 was evaluated during 2006-2007 field performance test. It showed better growth characteristics and yield performance than standard cultivar KF109. It had 2 more leaves per plant, flowered 2 days later than KF109. The yield of cured leaf of KF120 was increased by about 5% compared to KF109. The chemical composition and physical properties of the cured leaf of KF120 were as much acceptable as those of KF109. KF120 showed high resistance to PVY compared to KF109. It showed a similar mode of resistance to bacterial wilt and black shank as was found in KF109.
Cucumber mosaic virus (CMV) leads to a cause of poor crop productivity and quality. To solve this problem, we attempted to develop a virus-resistance tobacco plants by using viral coat protein (CP) gene. Transgenic tobacco plants expressing CMV CP gene were analysed by the resistance upon CMV infection. The virus-resistance was measured in $\textrm{T}_{1}$, generation by the inhibition of plant growth and the expression of the mosaic symptoms infected with CMV. The transgenic lines were divided into four groups: highly resistant, resistant, moderate and susceptible based on their growth and symptom severity. Out of 39 transgenic lines, 16 lines showed significant virus-resistance. And of resistant lines, 2 lines were designated highly resistant based on the facts that they achieved similar plant height to that of non-infected tobacco plants and showed lower disease symptom than that of other lines. The steady state level of CP RNA and coat protein level were measured by northern blot and immunoblot analysis. The CP RNA was highly accumulated in most resistant and moderate lines but barely detected in susceptible lines. The coat protein was detected in most lines regardless of their resistance to CMV. from this result, virus-resistance appeared to correlate more with CP RNA level than the level of coat protein. However, in two highly resistant lines, CP RNA level was unexpectedly low. This unexpected phenomenon need to be further investigated.
A field experiment was conducted to find out the effects of liming(soil pH) and sources of N on growing characters and yield of burley tobacco. Treatments consisted of liming(nonliming, liming to soil pH5.5 and 6.5) as the main plot and N sources(compound fertilizer of containing 3.9% NH$_4$-N and 6.1% NH$_2$-N, NaNO$_3$,(NH$_2$)$_2$CO and (NH$_4$)$_2$SO$_4$as the sub-plot. The growth of vegetative growing stage of limed plots were delayed(to compare the nonlimed plot) by influence of alkali. When the source on N was NaNO$_3$ the growth of vegetative growing stage was unfavorable and the yellowing of lower leaves of maturing stage was rapid. The yield and value of cured leaf was increased by increasing the rate of Ca(OH)$_2$, but there was no significant differences among the source of N. The yield response to liming was greater when the source of N was (NH$_4$)$_2$SO$_4$ than that of any other plots.
Influence of nitrate on growth, chlorophyll content, content and activity of rubisco and rubisco activase of tobacco plant cultured on MS medium treated with cadmium in vitro was studied. In vitro growth and chlorophyll content reduced at 0.2 mM Cd was recovered by nitrate and this recovery was most significant at 80 mM nitrate. Rubisco content at 80 mM nitrate was more increased compared to that at other concentrations. A similar change was also shown in rubisco activity. These resultsindicate that the activation and induction of rubisco reduced by Cd were recovered by nitrate. The degree of intensity of 55 and 15 kD polypeptides identified as the large and small subunits of rubisco by SDS-PAGE analysis at 80 mM nitrate was significantly higher than that at other concentrations. The content and activity of rubisco activase at 80 mM nitrate was significantly increased than that at other concentrations. These data suggest that the recovery effects of rubisco by nitrate may be associated with rubisco activase.
To determine the effects of mulching with the hulls of rice on the growth of the ginseng plant and changes of its growing environment-soil moisture content. subterranccan temperature and soil hardness- were investigated under different light intensity such as 5%, 10%, 20%, and 30% light transmittance rate(LTR). The results obtained were as follows; 1. Soil moisture content under the shading was decreased as the increase of light intensity, whereas it was increased about 1.5% in each plot of LTR by the mulching. 2. Suberranccan temperature under the shading was increased as the increase of light intensity. It was decreased on a hot day by the mulching but increased on a cold day. 3. Soil hardness was decreased by the mulching. 4. Sprouting date of the ginseng plants was acclerated for 7 days and sprout periods were shortened for f days by mulching compared to the non-mulching treatment. 5. Missing plant rate was increased severely as the increase of light intensity more Than 20% LTR In the non-mulching plots but did not severe in the mulching plots. Missing plant rate was decreased remarkably by the mulching. The degree of decrease was larger as the increase 6f light intensity. 6. Root yield was increased in the mulching plots compared to the non$.$mulching plots. The degree of increase was larger as the increase of light intensity. The highest yield was obtained at 20% LTR with mulching.
Park, Yong-Eui;Yang, Deok-Chun;Park, Kwang-Tae;Soh, Woong-Young;Hiroshi Sano
Proceedings of the Botanical Society of Korea Conference
/
1999.07a
/
pp.85-89
/
1999
Somatic embryogendesis is one of good examples of the basic research for plant embryo development as well as an important technique for plant biotechnology. This paper describes the direct somatic embryogenesis from zygotic embryos of Panax ginseng is reversely related to normal axis growth of zygotic embryos by the experiment of various chemical treatments. Under the normal growth condition, the apical tips of embryo axis produced an agar-diffusible substance, which suppressed somatic embryo development from cotyledons. Although the cells of zygotic embryos were released from the restraint of embryo axis, various factors were still involved for somatic embryo development. Electron microscopic observation revealed that the ultrastructure of cells of cotyledon epidermis markedly changed before initiation of embryonic cell division, probably indicating reprogramming events into the cells embryogenically determined state. Polar accumulation of endogenous auxin or cell-cell isolation by plasmolysis pre-treatment is the strong inducer for the somatic embryo development. The cells for the process of somatic embryogenesis might be determined by the physiological conditions fo explants and medium compositions. Direct somatic embryos from cotyledons fo ginseng were originated eithrer from single or multiple cells. The different cellular origin of somatic embryos was originated either from single or multiple cell. The different cellular origin of somatic embryos was depended on various developmental stages of cotyledons. Immature meristematic cotyledons produced multiple cell-derived somatic embryos, which developed into multiple embryos. While fully mature cotyledons produced single cell-derived single embryos with independent state. Plasmolysis pretreatment of cotyledons strongly enhanced single cell-derived somatic embryogenesis. Single embryos were converted into normal plantlets with shoot and roots, while multiple embryos were converted into only multiple shoots. GA3 or a chilling treatment was prerequisite for germination and plant conversion. Low concentration of ammonium ion in medium was necessary for balanced growth of root and shoot of plantlets. Therefore, using above procedures, successful plant regeneration of ginseng was accomplished through direct single embryogenesis, which makes it possible to produce genetically transformed ginseng efficently.
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