• 한국잡초학회지
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• 제11권1호
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• pp.68-73
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• 1991

담배 잎으로 부터 광독립영양세포(光獨立營養細胞) 육성방법(育成方法)을 확립(確立)하고자 식물생장조절제(植物生長調節劑) 및 sucrose 농도(濃度)와 빛이 담배의 세포(細胞) 배양(培養)과 배양(培養) 세포(細胞)의 엽록소(葉綠素) 생성에 미치는 영향(影響)을 조사하여 얻어진 결과(結果)를 요약(要約)하면 다음과 같다. 1. 담배 잎으로부터 callus 유도(誘導)에는 LS 기본(基本) 배지(培地)에 NAA $10^{-5}$M과 BA $10^{-6}$ M 을 혼합(混合) 처리(處理)하였을때 치상(置床) 후 30일째 3.08g으로 가장 높았다. 2. Callus의 엽록소(葉綠素) 함량(含量)도 LS 기본(基本) 배지(培地)에 NAA $10^{-5}$ M과 BA $10^{-6}$ M을 혼합(混合) 처리(處理)한 조합(組合)에서 28.42${\mu}g/g$.(FW)의 가장 높은 함량(含量)을 얻었다. 3. 광(光) 및 암조건(暗條件) 하(下)에서 sucrose 농도(濃度)가 0.5%에서 3.0%까지 증가(增加)할수록 callus 유도량(誘導量)이 증가(增加)되었으나 특히 광조건하(光條件下)에서는 sucrose 농도(濃度) 2.0%에서 가장 높았고 반면에 엽록소(葉綠素) 함량(含量)은 sucrose 농도(濃度) 0.5%에 가장 높았으며 암조건(暗條件) 하(下)에서는 엽록소(葉綠素)가 거의 형성(形成)되지 않았다. 4. 엽록소(葉綠素) 함량(含量)에 관(關)한 한 sucrose 농도(濃度)를 0.75%까지 낮추어도 sucrose 농도(濃度) 1.0%와 유사(類似)한 경향(傾向)을 보였다.

• 한국연초학회지
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• 제13권1호
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• pp.43-52
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• 1991

These studies were carred out to obtain the transformant from tobacco cells by Agrobacterium spp. from crown gall and soil at the natural field in Korea, and identified their virulence. Kodo's and Clark's selective media were used for isolation of Agrobacterium spp. In these media, total of 99 strains were characterized based on the morphological characteristics of colonies. Among them 34 strains were able to induce on carrot discs. And hypervirulent strains C23-1 and K29-1 were identified as Agrobacterium tumefaciens biotype 1 and biotype 2, respectively. These strains formed fast growing, larger gall as compared to those induced by other strains on the carrot discs. Transformed tobacco callus was initiated on the phytohormone free MS medium with 250$\mu\textrm{g}$/ml carbenicillin after co-cultivation of tobacco stem explants and Agrobacteria. On the phytohormone free media, shoot was rarely formed from transformed callus. However, these shoot were teratoma shoots which were not grown as normal shoot, and teratoma shoot from transformant by C23-1 was smaller than that of K29-1.

• 한국연초학회지
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• 제14권1호
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• pp.33-41
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• 1992

These studies were conducted to investigate effects of phytohormone and activated carbon on the growth and rooting of teratoma shoots induced from Nicotiana tabacum cv. NC2326 transformed by Aerobacterium tumefaciens C58. GA was effective for shoot elongation and reduction of multiple shoots from teratoma shoot, however, leaves of teratoma shoot cultured on the medium with GA were pointed. ABA was also effective in promoting shoot elongation, but was not for reduction of multiple shoots. Teratoma shoot cultured on the medium with 1 n activated carbon promoted shoot elongation and inhibited the number of shoots differentiated, but was grown as abnormal shoot. Addition of 1% activated carbon and 0.5mg/l BA to culture media was effective for shoot elongation and reduction of multiple shoot and for formation of round leaves as normal leaves. Though these shoots were inoculated on the rooting medium, they could not from roots but formed multiple shoots. Boric acid, myo-inositol and sucrose were also ineffective on the rooting of teratoma shoots.

• Biotechnology and Bioprocess Engineering:BBE
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• 제11권2호
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• pp.154-159
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• 2006

Interleukin-18 (IL-18), otherwise known as interferon-gamma-inducing factor (IGIF), is one of several well characterized and important cytokines that contribute to host defenses. The complementary DNA (cDNA) of mature human interleukin-18 gene (hIL-18) was fused with the signal peptide of the rice amylase 1A gene (Ramy1A) and introduced into the plant expression vector under the control of a duplicated CaMV 35S promoter. The recombinant plasmid was transformed into tobacco (Nicotiana tabacum L. cv Havana) using the Agrobacterium-mediated transformation method. The integration of the hlL-18 gene into the genome of transgenic tobacco plants was confirmed by polymerase chain reaction (PCR) amplification and its expression was observed in the suspension cells that were derived from the transgenic plant callus by using Northern blot analysis. The hlL-18 protein was detected in the extracts of the transgenic callus and in the medium of the transgenic tobacco suspension culture by using immunoblot analysis. Based upon enzyme-linked immunosorbant assay (ELISA) results, the expression level of the hlL-18 protein approximated $166{\mu}g/L$ in the suspension culture medium. Bioassay results from the induction of $interferon-{\gamma}$ from a KG-1 cell line indicated that the hlL-18 secreted into the suspension culture medium was bioactive.

• Plant Biotechnology Reports
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• 제4권1호
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• pp.53-59
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• 2010

A specific deleted version of ARABIDOPSIS RESPONSE REGULATOR1 (ARR1) lacking the signal receiver domain (1.152 amino acids)-coding sequence, referred to as $ARR1{\Delta}DDK$, was amplified using Arabidopsis thaliana cDNA prepared from adult leaves and transferred into the genome of Nicotiana tabacum cv. Samsun under the transcriptional control of a ${\beta}$-estradiol-inducible expression system. The ectopic expression of $ARR1{\Delta}DDK$ affected the morphology of transgenic seedlings and their segments in vitro. In the presence of an inducer, ${\beta}$-estradiol, ectopic expression of $ARR1{\Delta}DDK$ induced only the formation of soft, pseudo-bulbous tissue in the root tip region of intact seedlings, which appeared similar to callus generated on a hypocotyl segment in the presence of 2,4-D and 6-benzyladenine (BA), both at $1\;{\mu}M$. Those callus tissues on the root tip region could not generate shoots unless $1\;{\mu}M$ BA was supplied. In segment culture, ectopic expression of $ARR1{\Delta}DDK$ induced calluslike tissue around the cut-end of cotyledon and hypocotyl segments with occasional shoot formation, suggesting that the expression of $ARR1{\Delta}DDK$ could substitute for the effects of cytokinin on these segments. Additionally, treatment with only ${\beta}$-estradiol induced NtWUS, a WUS ortholog in tobacco, which was detected during the process of callus tissue formation in the root tip region and also in cotyledon or hypocotyl segments. These findings suggest that the NtWUS might be associated in the transdifferentiation process caused by the functional regulation of $ARR1{\Delta}DDK$ in transgenic tobacco seedlings.

• 고려인삼학회:학술대회논문집
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• 고려인삼학회 1984년도 학술대회지
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• pp.1-11
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• 1984

인삼의 대량증식 방법과 원형질체배양기술을 개발하기 위한 연구의 일환으로써 인삼의 자엽 callus 조직에서 많은 유식물체를 생산하는데에 미치는 식물생장조절물질의 영향을 구명하고, 또한 일반 식물과는 전혀 다른 인삼의 생존력이 있는 원형질체를 나출하여 배양할 수 있는 방법을 확립하고저 수행하였던 바 그 결과를 요약하면 다음과 같다. (1) Murashige & Skoog(MS) 배양기조성 성분의 반량($\frac{1}{2}MS$)에 2, 4 - D 0.5mg/$\ell$ Kinetin 0.5mg/$\ell$를 첨가한 배양기에서 가장 많은 양의 배상체가 유기되었다. (2) 유기한 배상체를 동일배기에서 계속 배양할 경우에는 다시 탈분화되는 경향을 보였으나 $\frac{1}{2}MS$ 배양기에 BA와 GA를 같은 농도(BA : GA=1 : 1)로 첨가한 배양기에 옮겨서 배양하였던 바 배상체의 발육이 진전되어 유식물체로 발달하였다. (3) 인삼은 1년근 세포에서 원형질체를 나출할 경우의 최적요건은 효소로서 cellulase $2\%$, macerozy-me $0.5\%$ 였으며, osmoticum으로서는 mannitol 0.9M, pH 5.2였고, 처리기간은 $28{\pm}1^{\circ}C$에서 $7\~8$시간이었다. (4) 인삼 callus조직세포에서 원형질체 나출할 시에는 cellulase $2\%$, macerozyme $2\%$, driselase $1\%$씩 첨가한 효소용액으로 28{\pm}1^{\circ}$에서 25시간 이상 처리하는 것이 나출원형질체의 수와 생존율면에서 볼 때 가장 적합한 것으로 사료되었다.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 1999년도 The 6th International Symposium on the Development of Anti-Cancer Resource from Plants
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• pp.46-57
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• 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.

• 한국식물학회:학술대회논문집
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• 한국식물학회 1987년도 식물생명공학 심포지움 논문집 Proceedings of Symposia on Plant Biotechnology
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• pp.357-389
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• 1987

In an attempt to clarify the physiological functions of individual isoperoxidases, we have studied enzymatic and immunological properties as well as cellular distribution of isoperoxidases from tobacco callus and Korean radish. The gene expression patterns of isoperoxidases in shoot and non-shoot-forming tobbaco callus were also examined by rabbit reticulocyte lysatein vitro translation system. These results indicate that fraction of translatable poly(A)-isoperoxidase mRNA was increased considerably in shoots. At the present time, at least 6-7 isoperoxidases could be detected from the translation mixture of total cellular RNA, among which only one cell wall localized anodic isoperoxidase (named A3) mRNA was bimorphic mRNA. These data suggest the possible regulation of peroxidase activity during shoot formation by altering the polyadenylation state of mRNA. In case of Korean radish seedlings, poly(A)- peroxidase mRNA were also increased depending upon aging.

• 환경생물
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• 제19권3호
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• pp.211-217
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• 2001

식물의 저항성과 방어관련물질 유도에 관련된 salicylate가 담배 미분화세포로부터 분리된 isoperoxidase $A_3$의 활성에 미치는 영향을 살펴보고, $Fe^{2+}$ 의 첨가에 의하여 salicylate에 의한 효소활성 억제가 보호되는 양상을 조사하였다. 다양한 농도의 salicylate가 isoperoxidase $A_3$의 활성에 미치는 영향을 조사한 결과 0.48mM salicylate에 의하여 isoperoxidase $A_3$의 활성이 약 20% 감소되었고, 0.6mM salicylate에 의하여 효소활성이 85% 이상 감소되었다. 이러한 결과는 salicylate에 의하여 isoperoxiase $A_3$가 억제됨을 보여준다. Salicylate에 의한 isoperoxidase $A_3$의 억제반응은 pH 의존적으로 일어났을 뿐만 아니라, noncompetitive inhibition 양상을 나타냈다. 뿐만 아니라 salicylate에 의한 isoperoxidase $A_3$의 활성억제는 $Fe^{2+}$ 첨가에 의하여 거의 완벽하게 보호되었다. Isoeroxidase A3로부터 heme부분을 제거하여 apoperoxidase를 제조한 후 여러가지 금속이온이 apoperoxidase의 활성회복에 미치는 효과를 조사하였다. 그 결과 hemin과 $Fe^{2+}$ 첨가에 의하여 apoperoxidase의 활성이 80% 이상 회복되었으나 $Cu^{2+},\;Zn^{2+},\;Co^{2+},\;Mn^{2+}$ 등은 apoperoxidase의 활성을 재구성시키지 못하였다.

• 한국연초학회지
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• 제27권2호
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• pp.153-162
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• 2005

Tobacco (Nicotiana tabacum L.) cells were transformed with rice expansin genes, OsEXPA4, OsEXPB3, OsEXPB4, and OsEXPB6, to elucidate the function of the genes in tobacco cells. The transformation increased the mass of the callus by $36\%-65 \%$, and the cell length by $12\%-28\%$. The cell width was decreased by $3\%$ for OsEXPB3, not changed for OsEXPB4, increased by $25\%\;and\;20\%$ for OsEXPA4 and OsEXPB6, respectively. From database search, seven expansin genes were found and six of them belong to EXPA group and one of them belongs to EXPB group. EXLA and EXLB were not found. All tobacco expansin genes were evenly distributed in the phylogenetic tree of rice and Arabidopsis expansin genes.