• 제목/요약/키워드: Flask-shaking

검색결과 63건 처리시간 0.031초

인 축적균 Acinetobacter CW3의 분리 및 특성 (Isolation and Characterization of Phosphorus Accumulating Acinetobacter CW3)

  • 심성훈;류원률;이영호;김정목;조무환
    • KSBB Journal
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    • 제14권1호
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    • pp.71-75
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    • 1999
  • 인 축적능이 우수한 균주를 자연계로부터 위노그라드스키 칼럼을 이용해 분리하여 Acinetobacter 속으로 동정하였고, Aci-netobacter CW3로 망명하였다. 인 축적균주의 배양초기조건은 $20^{\circ}C$. pH 7, 200rpm, 18.5mg $FO_4-P/\ell$가 최적임을 보였다. Acinetobacter CW3은 회분배양에서는 최적조건에서 12시간만에 인의 제거가 완료되었다. 이 균주는 호기조건에서는 인을 균주 내부에 과량 축적하고 첨가조건에서 인을 다시 방출함을 보였다.

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오미자의 형질전환된 근으로부터 리그난 화합물의 검출 (Detection of Lignans from Transformed Root Cultures of Schisandra chinensis Baillon)

  • 황성진;표병식;황백
    • 한국약용작물학회지
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    • 제12권6호
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    • pp.448-453
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    • 2004
  • Transformed roots of Schisandra chinensis were obtained following co-cultivation of in vitro cultivated plantlet segments with Agrobaterium rhizogens ATCC15834. This root was examined for its growth and gomisin J contents under various culture conditions. Among the six basal culture media tested, WPM (Lloyd & McCown, 1980) medium supplemented with 5% sucrose was the best roots growth 6.2 (g D.W/flask) and gomisin J accumulation 1.56 $(X10^{-3}\;ug/g\;D.W)$. Initial inoculum size correlated with the yield of biomass while gomisin J contents was not affect. Gomisin J production was influenced by the initial sucrose concentration and the highest production yield was achieved at the concentration of 7%. The optimal shaking speeds for roots growth and gomisin J production was 120 and 140 rpm, respectively.

해양미생물로부터 카로테노이드 색소의 생산을 위한 최적조건 (Optimal Growth Conditions for Carotenoid Pigment Production from marine Microorganism)

  • 정영기;김태수;정명주;류병호;주우홍;박정욱
    • 한국식품영양과학회지
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    • 제28권6호
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    • pp.1239-1243
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    • 1999
  • The optimal medium composition for the production of carotenoid pigment from Haloarcular sp. EH 1 as a dietary for fishes were 1.0% sucrose, 1.0% yeast extract, 25% sodium chloride, 0.3% sodium citrate, 0.2% potassium chloride, 2.0% magnesium sulphate, 0.002% ferric sulphate(pH 7.0). The incubation temperate, aeration rate and agitation speed were 40oC, 100ml medium/500ml vol. shaking flask, and 180 rpm/min. The carotenoid pigment production was highest after 5 days of incubation with the light.

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Polyoxyethylene monooleate 및 oleyther계 유분산제의 제조와 Bunker B유의 분산효율에 미치는 영향 (Preparation of Oil dispersants using polyoxyethylene Monooleate and Oleyether and its Effect on dispersing efficiency to Bunker B Oil)

  • 염규설;강두환
    • 한국응용과학기술학회지
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    • 제12권1호
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    • pp.59-67
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    • 1995
  • Oil dispersants using polyoxyethylene monooleate, polyoxyethylene oleylether, and poly(oxypropylene-oxyethylene)glycol block copolymer were prepared, and oil dispersant efficiency was measured using vertical shaking flask method to 4 kinds of Bunker B oil with different physical properties by appling the prepared dispersants. Although the dispersant efficiency was differed according to the differences of physical properties of Bunker B oil, the dispersant prepared using polyoxyethylene oleylether was the most effective to disperse the oil into water. The impurities like surfur contained in sample oil have to be removed by filteration to obtain the correct degree of absorption using UV spectrophotometer.

계면활성제 생분해도 측정방법에 관한 연구 (Studies on the Biodegradation Test Method of Sufactant)

  • 김영환;정해권김은기윤태일
    • KSBB Journal
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    • 제8권4호
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    • pp.364-369
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    • 1993
  • The biodegradability of some anionic surfactants were investigated using biological oxygen consumption measurement at different temperatures. As test surfactants, soap, alkyl sulfate (AS), alpha olefin sulfonate (AOS), alkyl polyoxyethylene sulfate (AES), linear alkylbezene sulfonate(LAS), microbial surfactants such as sophorose lipid (sopholipid) and spiculisporic acid (S-acid), were used. The test solution were incubated at $5^{\circ}C$, $18^{\circ}C$ and $32^{\circ}C$, respectively. The comparative rates of biodegradation were in accordance with the results obtained from the surface tension measurement and methylene blue method. The results of comparative blodegradabilities of the surfactants were as follows; soap, AS>AES>AOS>LAS at $18^{\circ}C$ and $32^{\circ}C$. However, at$ 5^{\circ}C$, the biodegradation rate of soap was better than other surfactants. Considering the actual environment of the river, it was concluded that the biological oxygen consumption rate method at lower temperature was more practical than the current method such as methylene blue assay with adapted shaking flask culture at $25^{\circ}C$

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환경친화적 미생물비료 자원 Pseudomonas fluorescens RAF15에 의한 가용성 인산 생산에 영향을 미치는 조건 (Conditions for Soluble Phosphate Production by Environment-Friendly Biofertilizer Resources, Pseudomonas fluorescens)

  • 박기현;박근태;김성만;이충열;손홍주
    • 한국환경과학회지
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    • 제17권9호
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    • pp.1033-1037
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    • 2008
  • The effects of inorganic salts, inoculum concentration, aeration rate and shaking speed on insoluble phosphate solubilization by Pseudomonas fluorescens RAF15 were investigated. Soluble phosphate production was dependent on the presence of $MgCl_2{\cdot}6H_2O$ and $MgSO_4{\cdot}7H_2O$ in the medium. Supplementation of medium with 0.01% $CaCl_2{\cdot}2H_2O$ and 0.01% NaCl slightly increased soluble phosphate production. The optimal medium compositions for the solubilization of insoluble phosphate by P. fluorescens RAF15 were 1.5% glucose, 0.005% urea, 0.3% $MgCl_2{\cdot}6H_2O$, 0.01% $MgSO_4{\cdot}7H_2O$, 0.01% $CaCl_2{\cdot}2H_2O$ and 0.01% NaCl, respectively. Optimal inoculum concentration was 2.0%(v/v). Maximum soluble phosphate production was obtained with 20-50 ml/250-ml flask and 200 rpm of shaking speed, respectively. The addition of EDTA decreased cell growth and soluble phosphate production.

함박꽃나무의 현탁배양세포로부터 [+]-Eudesmin의 생산을 위한 최적화 (Optimization of Culture Conditions for the [+]-Eudesmin Production in Magnolia Sieboldii Cells)

  • 황성진
    • KSBB Journal
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    • 제20권1호
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    • pp.34-39
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    • 2005
  • 목련과 수종인 함박꽃나무의 현탁배양세포로부터 생리활성을 갖는 리그난화합물인 (+)-eudesmin을 효율적으로 생산하기 위한 연구로써 플라스크배양 단계에서의 다양한 배양조건들 즉, 배지, 초기 당농도, 교반속도, 초기 접종농도, 그리고 elicitation 효과를 확인하고자 하였다. MS배지를 포함한 4종의 배지에서는 물질의 생산성과 생중량 모두에서 MS배지가 적합한 것으로 나타났다. 130 rpm으로 교반되는 항온배양기에서 $3\%$ sucrose와 0.5 mg/L 2,4-D가 첨가된 MS배지에 0.5 mg (DCW)의 농도로 세포를 접종한 실험구에서 8주 후 플라스크 당 3.71 g (DCW)의 생중량을 얻었으며, 지표물질인 (+)-eudesmin의 함량은 $5\%$ sucrose와 200 mg/L chitosan 처리구에서 $3.2{\mu}g/g$ (DCW)으로 대조구에 비해 1.7배의 증가를 나타내었다. 이와 같은 연구결과는 생물반응기를 이용한 목련과 수종에서의 유용물질 생산 연구에 활용될 수 있을 것으로 사료된다.

분광광도계를 이용한 점토함량 분석 (Use of Spectrophotometry for Quantitative Determination of Soil Clay Content)

  • 박순남;김계훈;강지영
    • Applied Biological Chemistry
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    • 제48권2호
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    • pp.183-188
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    • 2005
  • 토양 입경분석 중 점토함량 분석과정은 특히 시간과 공간을 많이 필요로 한다. 본 연구는 분광광도계(spectrophotometer)를 이용하여 점토함량을 측정하는 방법을 개발하고자 수행되었다. 분광광도계를 이용한 점토함량 분석방법은 다음의 4단계를 통해 개발되었다. 첫째, 분광광도계로 점토 분석이 가능한 최적파장을 선택하기 위해 표준 점토 시료(kaolinite, vermiculite, illite, montmorillonite)를 이용하여 점토종류에 따른 파장별 흡광도를 측정하였으며, 최적 파장으로 500 nm를 선정하였다. 둘째, 분광광도계를 이용한 재현성이 높은 분석 방법은 250 ml 삼각 플라스크에 풍건 토양과 분산액을 넣고 12시간 진탕(130 rpm)하여 토양시료를 분산시킨 후 용기를 30초간 상하로 흔들어 미리 설치한 cell에 4 ml를 피펫으로 취하여 즉시 흡광도를 측정하는 것으로 조사되었다. 셋째, 점토함량 정량 분석을 위해 검정선(calibration curve)을 작성하였다. 넷째, 분광광도법(spectrophotometry)으로 분석된 동일 시료의 점토함량을 표준 방법으로 알려진 피펫법(pipet method)으로 분석한 후 회귀분석을 실시하여 분광광도법으로 측정한 점토함량을 피펫법으로 분석한 결과로 환산하는 환산식을 유도하였다. 분광광도법으로 측정한 점토함량은 토양시료내에 포함된 유기물 함량과도 상관관계가 조사되어 피펫법으로 측정한 점토함량과 분광광도법으로 측정한 점토함량, 유기물 함량간의 다중 회귀분석을 실시하였다. 그 결과 회귀방정식은 $y\;=\;38.03x_1-0.17x_2-1.17$(y = 피펫법으로 측정한 점토함량(%); $x_1$ = 분광광도법으로 측정한 점토함량(%); $x_2$ = 유기물 함량($g{\cdot}kg^{-1})$)이었으며, 상관계수는 $0.984^{**}$로 두 방법사이에 높은 상관관계가 있는 것으로 조사되었다. 여기서 유도된 회귀방정식을 프로그램화하여 컴퓨터나 분석기기에 입력시 시간과 공간을 절약하고 신속하고 정확하게 점토함량을 분석할 수 있을 것으로 판단된다.

오이조직 배양세포에 의한 Ascorbate Oxidase 생성 및 생산 (Formation and Production of Ascorbate Oxidase by Cucumber Tissue Cultured Cells)

  • 이종화;정호권;;임번삼
    • 한국미생물·생명공학회지
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    • 제21권4호
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    • pp.329-335
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    • 1993
  • Ascorbate oxidase activity in various cucumber tissue extracts was highest in young fruit peeling. Cucumber callus was induced from young fruit peeling and callus cell lines were selected for more than 7 months, which porduced high levels of ascorbate oxidase and had a high growth rate. Induction of callus was optimized with Linsmaier-Skoog(LS) medium at 25$^{\circ}C$ in dark phase. Ascorbate oxidase activity reached a maximum at 5 days after transfer to LS basal liquid-medium ant then declined. The enzyme activity in callus cells was stimulated by addition of 10${\mu}$M $CuSO_4$ in the early logarithmic phase of growth. And also, adding 10${\mu}$M $CuSO_4$ at 3rd day 7th day of culture period, ascorbate oxidase activity in callus cells was maintained to high level. Maximum yield of ascorbate oxidase was found at the 25th day by flask shaking culture, but three-fold of ascorbate oxidase activity was obtained at the 16th day by jar fermentation.

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해양유류오염 방제를 위한 생물유화제 생산세균의 분리 및 특성 (Isolation and Characterization of a Bioemulsifier-Producing Bacterium for Marine Oil Spill Bioremediation)

  • 손홍주;차미선
    • 한국환경과학회지
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    • 제6권5호
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    • pp.473-480
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    • 1997
  • Microorganisms producing bioemulslfiler were isolated from the sea water In Pusan coastal area. The isolated strain which had the highest emulsification activity and stability was identified as the genus Achetobacter from the results of morphological. cultural and biochemical tests and named Achetobacter sp. EL-C6 for convenience. The compositions of optimum medium for emulsification of crude oil by Acinetobacter sp. EL-C6 were crude oil 2.0%, NH4NO3 0.2%, $K_2HPO_4$ 0.01%, $MgSO_4$.$7H_2O$ 1.o%, $CaCl_2$.$2H_2O$ 0.1% and NaCl 3.0% at initial pH 7.5 and 3$0^{\circ}C$, respectively. The cultivation for emulsification of crude ell was carried out in 500m1 shaking flask containing 100m1 of the optimum medium at 3$0^{\circ}C$. The highest emulsification was observed after 5 days. The utilization on the various hydrocarbon of the Achetobacter sp. EL-C6 showed that utilization of n-alkane compounds were better than that of aromatic compounds. Among the petroleum compounds, crude ell was best utilized by the Achetobacter sp. EL-C6.

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