• 제목/요약/키워드: suspension cell culture

검색결과 373건 처리시간 0.025초

Kinetic Analysis of the Effect of Cell Density on Hybridoma Cell Growth in Batch Culture

  • Lee, Eun-Yeol
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제7권2호
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    • pp.117-120
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    • 2002
  • The effect of cell density on cell growth was investigated in a suspension batch culture of hybridoma cells. The specific growth rate was found to increase with increasing initial cell density and then to decrease with further increases in initial cell density. In order to quantitatively describe the dependence of specific growth rate on cell density, a kinetic model is proposed, which satisfactorily represents the experimental data.

Peppermint 세포 현탁배양에서 Cyclodextrin을 이용한 Menthol의 생산성 증대 (Production Enhancement of Menthol in Suspension Cultures of Peppermint Using Cyclodextrin)

  • 조규헌;임철호;박세춘;신명근
    • KSBB Journal
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    • 제13권1호
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    • pp.26-30
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    • 1998
  • The suspension cultures of Mentha piperita produce menthol which has very low solubility in water due to its hydrophobicity. This can be considered as a factor for its low production in the suspension suspension cultures. Cyclodextrin has the hydrophobic cavity inside the molecule in which menthol can be captured and allow to form a stable complex. The suspension culture of Mentha piperita showed 70% higher production enhancement in the medium containing 1.5%(w/v) $\beta$-cyclodextrin than the control. $\beta$-cyclodextrin had no adverse effect on the cell growth and showed the best result among $\alpha$-, $\beta$- and $\gamma$-cyclodextrins tested in terms of menthol production. We demonstrated that $\beta$-cyclodextrin can be used to enhance the production of menthol in the suspension cultures by capturing hydrophobic menthol into the cavity of cyclodextrin molecules.

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Studies on the Production of Bioactive Substances -Callus Culture of Rehmanniae Radix-

  • Chi, Hyung-Joon;Kim, Hyun-Soo;Cho, Hi-Jae
    • 생약학회지
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    • 제25권1호
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    • pp.28-30
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    • 1994
  • The rate of growth and production of bioactive substances from Rehmannia glutinosa Liboschitz (Scrophulariaceae) were studied with the variation on the constituents of the culture media. The best growth was observed from MS basal medium containing 3.0 ppm NAA and 2.0 ppm kinetin. Carbohydrates (fructose, glucose and sucrose), phytosterols(${\beta}-sitosterol$, campesterol and stigmasterol) and carotenoid like substances were identified by GC-MS and TLC from the callus mass. However, catalpol was not detected from both solid and cell suspension cultures containing geraniol. Callus cultured Rehmannia glutinosa in the MS basal medium containing 0.1 ppm NAA and 0.1 ppm kinetin become differentiated to root.

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Effect of Environmental Factors on Flavonol Glycoside Production and Phenylalanine Ammonia-lyase Activity in Cell Suspension Cultures of Ginkgo biloba

  • Kim, Min-Soo;Lee, Won-Kyu;Kim, Hwa-Young;Kim, Chul;Ryu, Yeon-Woo
    • Journal of Microbiology and Biotechnology
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    • 제8권3호
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    • pp.237-244
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    • 1998
  • A study was carried out to elucidate the relation between the production of flavonol glycosides and the change of phenylalanine ammonia-lyase activity in cell suspension cultures of Ginkgo biloba by the unassisted and synergistic effects of various factors. The quercetin production showed a mixed-growth-associated pattern in cell suspension cultures. Fluorescent light and UV radiation increased phenylalanine ammonia-lyase (PAL) activity, and resulted in the increase of the production of quercetin and kaempferol ten- and four-fold, respectively, as compared to that obtained in the normal culture condition. The cell growth of Ginkgo biloba was enhanced .at higher temperatures whereas the quercetin production was at its maximum at low temperatures. Moreover, the quercetin production was increased by temperature change during the culture period. In particular, the quercetin production was at the highest level when the culture temperature was elevated from $10^{\circ}C\;to\;30^{\circ}C$. The addition of phenylalanine as a precursor in the culture medium stimulated an 8-fold increase in the production of quercetin; the addition of naringenin caused a l0-fold increase. The quercetin production was also greatly increased by feeding enzyme cofactors such as 2-ketoglutarate and ascorbic acid in the culture medium, but specific PAL activity was not increased except with phenylalanine feeding. The synergistic effect of UV radiation and naringenin feeding was observed, resulting in the increase of flavonol glycoside production at a rate higher than in any other case investigated.

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포도와 미국자리공의 세포현탁배양계에 있어서 배지내 무기염 농도가 색소축적에 미치는 영향 (Effects of Salt Concentrations on Accumulation of Pigments in Cell Suspension Cultures of Vitis vinifera and Phytolacca americana L.)

  • 인준교;이영복;최관삼
    • 농업과학연구
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    • 제20권1호
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    • pp.34-42
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    • 1993
  • 포도 및 미국자리공의 세포현탁배양계에서 세포생장 및 색소축적에 미치는 배지내 무기 염농도의 효과를 알아 보았다. 포도의 세포 증식은 control구에서만 정상적인 대수증식기를 보였고, 희석배지에서는 4일째에서 6일째까지 완만한 대수증식기를 나타냈다. Anthocyanin은 모든 처리구에서 배양후 12일째에 최대로 축적이 되었다. 미국자리공에 있어서는 모든 처리구에서 세포증식과 동조적으로 betacyanin이 축적되어, 배양 8일 이후에 최대축척을 나타냈다. 포도의 세포배양에서는 sucrose 87.6mM까지는 세포증식이 증가하였으나 그 이상의 농도에서는 증식이 급격히 떨어졌다. Anthocyanin은 146mM에서 최대로 축적되었으며 그 이상의 농도에서도 다량의 anthocyanin이 축적되었다. 미국자리공에서는 sucrose농도가 높아질수록 세포증식 및 색소축적이 증가하는 경향을 보여, 포도의 배양세포와 대조적 인 결과를 보였다. 이상의 결과로써 포도의 anthocyanin과 미국자리공의 betacyanin이 같은 적색색소이지만, 배양세포내에서의 생성기작 및 그 축적과정이 서로 상이하다는 것을 보여주었다.

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야생 흰 제비꽃(viola patrinii DC.)callus의 현탁배양 방법이 세포 활성에 미치는 영향 (Effect of Suspension Culture Conditions on Cell Activity of Wild Viola(Viola partrinii DC.) Callus)

  • 김두현;정용모;정정한;이인;권오창
    • 생명과학회지
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    • 제6권2호
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    • pp.94-103
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    • 1996
  • To understand effect of inoculum size, cell density, sucrose concentration and concentrations of MS basal on suspension culture and protoplast isolation of wild viola(Viola patrinii DC.) callus from petiole segments this experiment was conducted. In the lot of 30 mesh inoculum size, two observations were; One was that a considerable increase in the fresh and dry weight of callus was determined. Another was that the callus mass was relatively compact compared with others. A recommendable cell density was 0.4g for 20ml culture medium and the higher sucrose concentration, the higher fresh and dry weight were obtained. The dilution of MS basal salt was differently affected on fresh and dry weight; the highest fresh weight was found in 1x MS salt, while the higest dry weight was in 1/3x dilution.The addition of casein hydrolysate(3g/L) was more effective to increase of both fresh and dry weight. THe contents of protein was great in the inoculum lots with larger inoculum sizeand higher concentration of MS basal salts contenting 3g/L of casein hydrolysate and higher sucrose compared with others. The greatest protoplasts were isolated from the lot of 10 mesh size treated with 1%pectinase SE-150 and 2% cellulase YC. In general, for optimal protoplast isolation the followingconditions were recommended; 1) Use of smaller cell size cultured for 2-5 weeks, and 2) more than 5 hours incubation using the combined mixture of the enzymes with proper concentrations.

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An Optimization of Flavonoid Production from the Suspension Culture of Scutellaria baicalensis Georgi Cells

  • SEO, WEON-TAEK;YOUNG-HOON PARK;TAE-BOO CHOE
    • Journal of Microbiology and Biotechnology
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    • 제6권5호
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    • pp.347-351
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    • 1996
  • Flavonoid production by suspended cells of Scutellaria baicalensis Georgi was studied and the medium was optimized for cell growth and baicalin production. In SH medium the flavonoid production was not closely associated with the cell growth. A modified SH medium, FPM, was therefore designed for enhanced baicalin production. In FPM, both cell growth and baicalin production were increased by 1.5 times and 1.67 times than in the original SH medium, respectively. The increases could be attributed to the increased metabolic activities involved in the flavonoid biosynthesis as represented by enhanced activities of phenylalanine ammonia-lyase.

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베큘로 바이러스 발현 시스템에 의한 곤충세포에서의 인간 트롬보포이에틴 생산 최적화 (Optimization of Human Thrombopoietin Production in Insert Cells Using Baculovirus Expression System)

  • 고여욱;손미영;박상규;안혜경;박승국;박명환;양재명
    • KSBB Journal
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    • 제13권2호
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    • pp.181-186
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    • 1998
  • 부착의존성 세포주인 Trichoplusia ni 의 유래의 BTI-TN5B1-4 (TN5) 곤충세포주를 이용하여 인간 혈소판생성축진인자인 재조합 인간 트롬보포이에틴(rhTPO)의 배양조건 최적화 연구를 수행하였다. 배양배지, 세포감염에 투입되는 재조합 베큘로바이러스와 숙주세포의 비율(MOI),세포감염시 세포밀도, 배지 회수시간 및 배양방법 등이 rhTPO 의 생산에 미치는 효과를 연구하여 60 mm dish로 정체 배양시 10 MOl 이상,$2\times10^6$ cells 의 세포밀도,바이러스 감염 후72 시간에서 rhTP0 의 최대 발현양 (약 12 mg/L)을 나타내었다. 배양 배지로서는 EXCELL FIVE 배지가 SF900II나Insect serum free media-1 Figure 5. Effect of growth phases on rhTPO production. TN5 cells were grown as suspension culture in 1 L spinner flask with 200 mL of SF900II serum free medium at 80 rpm. The cells were infected with AcBac404-2 at MOl of 1. Culture medium was collected at given time intervals and the expression level of rhTPO was analyzed by ELISA (A) or immunoblot analysis (B). Lanes 1 and 7; cell density of $0.6\times10^6$ cells/mL, lanes 2 and 8; cell density of $1.6\times10^6$ cells/mL, lanes 3 and 9; cell density of $2.0\times10^6$ cells/mL, lanes 4 and 10; cell density of $3.0\times10^6$ cells/mL, lane M; prestained molecular weight marker (Bio-Rad). Lanes 1, 2, 3, and 4; culture medium was collected at 48 hpi and lanes 7, 8, 9, and 10; culture medium was collected at 72 hpi. Figure 6. Effect of culture media on rhTPO production. TN5 cells grown with different culture media were infected with AcBac-404-2 at 10 MOL 10$\mu$L of culture medium was run on SDS-PAGE and Immunoblot analysis was performed. Lane ];TN5 cells cultured with SF900II serum free media(Gibco),and lane 3; TN5 cells cultured with EXPRESS FIVE serum free media (Gibco) 에 비해 더 증가된 발현양을 나타내었다. TN5 세포주를 0.2 L 규모 (1 L spinner flask)oJl에서 세포간의 응집현상 없이 부유배양에 적응,배양시킨 후 세포성장 시기에 따른 발현을 조사한 결과 1 MOI의 감염조건 하에서는 $0.6\times10^6$cell/mL의 early exponential시기의 세포밀도에서 72시간 배양하였을 대 최대 발현양을 나타내었다. 나타내었다.

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Agrobacterium을 이용한 형질전환 벼 현탁 세포주에서 miraculin 단백질의 생산 (Production of miraculin protein in suspension cell lines of transgenic rice using Agrobacterium)

  • 김희경;고지윤;박소영;강권규;정유진
    • Journal of Plant Biotechnology
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    • 제47권3호
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    • pp.227-234
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    • 2020
  • 벼(Oryza sativa L.)에서 세포 현탁 배양을 통한 miraculin 단백질의 생산을 위해 miraculin 유전자(AB512278)가 도입된 Agrobacterium tumefacience EHA105를 매개로 벼 캘러스에 형질전환하였다. 현탁배양세포주는 형질전환 캘러스를 이용하여 몇번의 선발과정 및 계대배양을 통해 선발하였고, 게놈 PCR 분석을 통해 miraculin 유전자가 벼 염색체에 안정적으로 도입된 것을 확인하였다. 또한, RT-PCR 분석을 통해 형질전환 세포주에서 도입된 miraculin 유전자가 과발현 되었다. 재조합 miraculin은 형질전환 현탁배양 HK-2 세포주에서 가장 높게 발현되어 total soluble protein (TSP) 대비 2.0%를 보였다. 이러한 결과는 형질전환 현탁세포배양이 miraculin과 같은 미각 수식 단백질의 대량생산 시스템을 구축하는데 이용 가능 할 것으로 사료된다.

강낭콩의 현탁배양시 증식과 세포벽 다당류 전환에 미치는 생장조절제 및 질소원의 장기간 효과 (Long-Term Effects of Growth Regulators and Nitrogen Sources on Proliferation and Turnover of Cell Wall Polysaccharides in Suspension Culture of Kidney Bean (Phaseolus vulgaris L.))

  • CHAI, Youn Kyung;KIM, Kyong Ho;YEO, Up Dong;SAKURAI Naoki
    • 식물조직배양학회지
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    • 제25권6호
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    • pp.477-485
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    • 1998
  • 감자 plastid 형질전찬을 위한 새로운 DNA 절편을 확보하고자, 감자의 trnK-matK 유전자를 PCR 방법으로 클로닝하고 특성을 조사하였다. 염기서열 분석을 통하여 trnK-matK 유전자에는 두 종류의 polymerase 인지부위[Prokaryotic site(plastid encoded polymerase)와 eukaryotic site (nuclear-encoded polymerase)]가 족재함을 알 수 있었다. 이 사실은 trnK-matK 유전자의 발현이 광합성조직과 비광합성조직에서 서로 다른 polymerase에 의하여 조절됨을 시사하였다. 한편 MatK의 아미노산서열을 분석한 결과 식물에 따라 아미노산 identity가 39-75%로 다양하였으나, 감자와 담배는 98%의 아주 높은 identity를 보였다. Northern분석을 통하여 포장과 기내에서 생육된 감자 식물체 모두에서, trnK-matK 의 전사 수준이 잎에서 높고 괴경에서는 낮음을 알 수 있었다. 한편 잎에서의 16s rDNA의 전사수준은 괴경에 비해 약 50배 높았다. 이것으로 미루어보아 괴경에서 수준이 낮을 것은, 괴경에서는 plastid genome copy 수가 적거나 plastid 수가 적기 때문으로 추정된다. 이상의 결과로서 엽록체와 amyloplst 모두에서 trunK-matK 유전자가 활발하게 발현되고 있음을 알 수 있었다. Plastid genomic DNA의 Southern 분석을 통하여 trnK는 1 copy로 존재하고, matK는 trnK intron을 포함하고 있음을 확인하였다. 따라서 감자 plastid형질전환의 새로운homologous recombination 부위로 trnK-matK유전자를 이용할 수 있을 것이다.

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