• Title/Summary/Keyword: $^{35}S$

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Plant Protein Improvement by Synthetic Gene (합성유전자를 이용한 식물단백질의 향상)

  • 김태금;양문식
    • KSBB Journal
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    • v.7 no.3
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    • pp.155-160
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    • 1992
  • To improve the nutritional quality of plant proteins, a synthetic gene, called HEAAE (high essential amino acid encoding)-DNA, was introduced and expressed in tobacco plants. The synthetic gene, which is 292 basepair-long, codes for a protein composed of about 80% essential amino acids. To improve its expression level in plants, Cauliflower Mosaic Virus (CaMV) 355 and CaMV duplicate 35S promoters which are known as strong promoters were used with Nopaline Synthase promoter as a control. Transformed and regenerated tobacco plants were subject to analysis for introduction and expression of this gene. Integration of the gene into the plant genome and its expression into mRNAs and its proteins have been demonstrated using Southern, northern blot analysis and amino acid analysis. The differences of expression levels among CaMV duplicate 35S, CaMV 35S and Nopaline Synthase promoters are significant in term of mRNAs, but not in terms of proteins.

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A Study on the Amorphous Phase Change of Obliquely Deposited $As_{40}Se_{15}S_{35}Ge_{10}$ Thin Films (증착각도에 따른 $As_{40}Se_{15}S_{35}Ge_{10}$박막의 비정질상 변화에 관한 연구)

  • 정홍배;김종빈;이현용;박태성
    • Journal of the Korean Vacuum Society
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    • v.2 no.1
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    • pp.85-91
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    • 1993
  • 본 연구에서는 광기록 매질 중 광유기효과가 큰 비정질 As40Se15S35Ge10박막의 증착각도변화에 따른 구조 및 광학적 구조 및 광학적 물질특성에 대해 고찰하였다. 준비된 bulk와 박막이 비정질상(Amorphous phase)임을 XRD 분석을 통해 확인하였다. 특히, 증착각도의 변화에 따른 비정질 As40Se15S35Ge10박막에서의 유리질 천이온도의 변화와 상분리 현상을 연구하였다. 유리질 천이온도의 확인은 DSC, DTA, TGA를 이용한 분석실험을 통해 수행하였다. 실험 결과 벌크의 유리질 천이 온도는 약 $238^{\circ}C$였고, 0。, 60。, 80。로 증착된 박막은 각각 $202^{\circ}C$, $229^{\circ}C$, $201^{\circ}C$였으며 80。로 증착된 박막의 경우 가장 낮은 값을 보였다. 또한 연속상과 분산상으로의 상 분리 현상은 편광현미경에 의한 광학구조분석과 SEM-EDS를 이용한 표면확인 및 성분분석으로 관찰하였다.

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Expression and Inheritance Patterns of Gus Gene Driven by an Endosperm-Specific Promoter in Transgenic Tobacco (배유 특이 프로모터에 의해 유도된 GUS 유전자의 형질전환 담배 내에서의 발현 및 유전 양상)

  • Park, Young Doo;Kim, Hyoung Seok
    • Horticultural Science & Technology
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    • v.18 no.5
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    • pp.594-598
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    • 2000
  • This study was carried out to investigate the tissue-specific expression of ${\beta}$-glucuronidase (gus) gene driven by endosperm-specific promoter (Z4 promoter) in the transgenic tobacco and to find out inheritance pattern of transgene to the next generation. Tobacco (Nicotiana tabaccum cv. Havana SR1) was transformed with Agrobacterium tumerfaciens LBA4404 harboring BV3 construct containing gus gene driven by Z4 promoter and a kanamycin resistant gene. Seven hundred bp PCR products, indicating the presence of npt II gene, were found in the all eight transformants by PCR analysis using nptII primers. To study the expression pattern of the two different kind of promoters, leaf disks of the Z4pro-gus-transformed plants and 35Spro-gus-transformed plants were analyzed histochemically for gus activity. As a result, leaf disks of Z4pro-gus-transformed plants showed very weak and partial positive gus activity. In contrast, leaf disks of 35Spro-gus-transformed plants showed relatively strong positive gus activity. To investigate the expressed position of Z4 promoter, seeds from Z4pro-gus-transformed plants and 35Spro-gus-transformed plants were analyzed histochemically for gus activity. Z4pro-gus-transformed seeds showed positive gus activity restricted to the endosperm. However, the blue-colored product in 35Spro-gus-transformed seeds was observed in all the area including endosperm. Kanamycin resistance assay showed that transgenes were stably inherited to next generation in all lines.

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Design of MMIC 2 Stage Power amplifiers for 35 ㎓ (35 ㎓ MMIC 2단 전력 증폭기 설계)

  • 이일형;채연식
    • Proceedings of the IEEK Conference
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    • 1998.10a
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    • pp.637-640
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    • 1998
  • A 35 ㎓ GaAs MMIC power amplifier was designed using a monolithic technology with AlGaAs/InGaAs/GaAs power PM-HEMTs, rectangualr spiral inductors and Si3N4 MIM capacitors. The GaAs power MESFETs in the input and output stages have total gate widths of 120 um and 320 um, respectively. Total S21 gain of 10.82dB and S11 of -16.26 dB were obtained from the designed MMIC power amplifier at 35 ㎓. And the chip size of the MMIC amplifier was 1.4$\times$0.8 $\textrm{mm}^2$

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Wind Fragility for Urban Street Tree in Korea (강풍 발생 시 국내 가로수의 취약성 분석)

  • Sim, Viriyavudh;Jung, WooYoung
    • Journal of Wetlands Research
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    • v.21 no.4
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    • pp.298-304
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    • 2019
  • In this paper, the analytical method to derive wind fragility for urban street tree in Korea was shown. Monte Carlo Simulation method was used to determine the probability of failure for urban street tree. This probability result was used to determine wind fragility parameters for four types of tree based on the study of street tree species in urban area in Daegu, Korea. Wind fragility for street tree was presented in terms of median capacity and standard deviation of the natural logarithm of the capacity. Results showed that the dominant factor affecting the probability of failure of tree under wind load was their diameter. Moreover, amongst the four types of tree chosen, the tree with height 7m and diameter 35cm had the lowest probability of failure under wind loading, whereas the tree with height 8m and diameter 30cm could resist the least wind loading. The median failure wind speed for urban street tree with height 7m were 43.8m/s and 50.6m/s for diameter 30cm and 35cm, respectively. Also, for tree with height 8m, their median failure wind speeds were 38.7m/s and 45.4m/s for tree with diameter 30cm and 35cm, respectively.

Development of a Plant Transformation Vector, pKCHI (고등식물 형질전환용 유전자 운반체 pKCHI의 개발)

  • 정상호
    • Journal of Plant Biology
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    • v.32 no.1
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    • pp.23-32
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    • 1989
  • We have developed a plasmid vector, pKCH1, for the purpose of higher plant transformation. It contains the promoter region of cauliflower mosaic virus 35S transcript (P35s) and the terminator region of nopaline synthase gene (Tnos) with unique cloning sites, Bam HI and Xba I, between them. After inserting a foreing gene at the cloning sites, P35s-foreign gene-Tnos cassette can be recovered by using a restriction enzyme Hind III.

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Effects of absorbed radioactive sulfur (S35) in plant cell. I. Mitotic chromosome aberrations in rye seedling induced by the treatment of S35 solution (식물에 미치는 방사성 동위원소 S35의 영향에 대하여 (제1보) 호밀 근단세포의 염색체 이상수발에 관한 연구)

  • 홍순우
    • Journal of Plant Biology
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    • v.8 no.1_2
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    • pp.1-4
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    • 1965
  • Beta-ray irradiation effects on structural changes of the chromosomes in root tip of rye, Secale cereale L., seedlings, particularly the frequency of chromosome bridge induction at anaphase stage treated with radioactive sulfur (S35) solutions were studied in this experiment. Among the four different concentrations of isotope solution, the lowest one, 0.4$\mu$c solution, has shown weak effect on the induction of chromosome aberration. On the other hand, higher concentration, 25.6$\mu$c solution, induced higher frequency of chromosome bridge induction as much as 4.3%. Concerning the relationship between the ages of after treatment and the ranges of concentration, the higher concentrations showed more pronounced effects than the lower ones.

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Expression Patterns of CaMV 35S Promoter-GUS in Transgenic Poatoes and Their Clonal Progenies

  • Lee, Kwang-Woong
    • Journal of Plant Biology
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    • v.37 no.1
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    • pp.17-25
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    • 1994
  • Two potato (Solanum tuberosum L.) cultivars were transformed by Agrobacterium tumefaciens harboring cauliflower mosaic virus (CaMV) 35S promoter and $\beta$-glucuronidase (GUS) gene. Expression patterns of the CaMV 35S promoter according to tissue types and developmental stages, and genetic stability of GUS gene were investigated in the clonal progenies of transgenic potatoes. Kanamycin-resistant shoot emerged from tuber disc after 4 weeks of culture, and root was induced 6 weeks after culture on the selection medium. Shooting frequency of cvs. Superior and Dejima were 43% and 27%, respectively. Mature transformants and their clonal progenies showed no phenotypical abnormality. GUS activity was expressed primarily at parenchymatous cells of phloem tissue around the vascular cambium in the stem and root, and higher activity was found at the apical meristem of shoot, root and adventious shoot bud. GUS activity was higher at tubers of young explants than at stored tubers. These facts indicate that expression level of the CaMV 35S promoter differed according to tissue types and developmental stages of the organs. The GUS gene was stably inherited to each clonal progeny and normally expressed.

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