• 식물조직배양학회지
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• 제27권6호
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• pp.447-451
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• 2000

나리‘Gelria’의 인편에서 캘러스를 유도, 증식시키고, 증식된 캘러스에서 식물체를 재분화하여 캘러스를 통한 재분화 기술체계를 확립하고자 실험한 결과, 인편에서 캘러스의 유도는 생장조절제가 전혀 첨가되지 않은 배지에서도 유도되었고, kinetin 0.5 ∼ l.0 mg/L와 NAA 0.1 ∼ l.0 mg/L가 첨가된 배지에서는 유연성이 높은 캘러스가 100%유도되었다. 생장조절제가 첨가되지 않은 배지에서도 캘러스의 증식이 양호하였으며, 생장조절제가 첨가된 배지에서는 증식률이 높아 캘러스가 왕성하게 증식되었다. 또한 캘러스로부터 신초가 발생하여 캘러스의 증식과 신초의 재분화가 동시에 발생하였다. 캘러스는 암배양보다는 명배양에서, 액체배양보다는 고체배양에서 더 잘 증식하였다. 생장조절제가 첨가된 배지에서는 캘러스가 왕성하게 증식하였고 신초의 재생은 생장조절제가 첨가되지 않은 배지에서 높았고, 다음으로 1.0mg.L의 BA와 NAA가 첨가된 배지에서 높았다.

• Applied Biological Chemistry
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• 제50권1호
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• pp.77-81
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• 2007

인산가용화균 Aspergillus sp. PS-104를 생물비료화하기 위하여 이 균주의 액침배양 시 mycelial pellet 형성을 억제하는 배양조건(배지 종류, 초기접종량)과 배지 첨가물(점토광물, 계면활성제, PEG 200)의 종류에 대하여 조사하였다. 그 결과 이 균주는 배지 종류를 달리하여 배양했을 때 SDB=YPD>PDB 순으로 pellet 크기가 감소하였다. 또한 이 균주는 $1{\times}10^{3}{\sim}1{\times}10^{7}$ conidia/ml 범위의 초기접종농도에서는 농도가 높을수록 pellet의 크기가 감소하였다. 또한 bentonite를 제외한 점토광물인 zeolite, diatomite, 황토, kaoline과 talc를 0.1% 농도로 배지에 첨가하였을 경우 pellet 크기가 대조군에 비해서 1/6${\sim}$1/4로 감소하였다 계면활성제인 Tween 80과 Triton X-100 및 PEG 200을 0.1% 농도로 첨가하였을 경우 pellet의 크기가 감소하였고, SDS를 첨가한 경우에는 균의 성장이 완전히 저해되었다.

• 환경위생공학
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• 제15권1호
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• pp.39-45
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• 2000

The purpose of this study was conducted to indentified the fixing quality of $CO_2$, the most important greenhouse effect gas, by microalgae Chlorella ellipsoidea in batch test apparatus. The glass flask of $1.4{\ell}$ culture media which was saturated with 99.99% pure $CO_2$ gas was setted water bath of $25^{\circ}C$, 5000Lux, and seeded 100$m\ell$ algae liquid. We checked the change of inorganic carbon concentration and algae population with time in culture media. The result were next: the growth of algae population relied on aquatic IC(inorganic carbon) concentration. And the pH was increased with decrease of IC concentration. The growth of algae population had positive correalation with $CO_2$ concentration, and the coefficient of correlation was 0.982. The specific growth rate($\mu$) of Chlorella ellipsoidea was 1.104/d, the maximum specific growth $rate({\mu}_{max}$) of 9.21/d, and helf velocity constant($K_s$) of $259mg/{\ell}$ by Monod equation.

• 한국균학회지
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• 제11권1호
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• pp.23-26
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• 1983

Aspergillus ustus의 dextranase을 정제하기 위하여 냉각 Aceton에 침전시키고, DEAE-cellulose, Bio-Gel P-150 및 Sephadex G-200을 사용하며 순수정제하였다. 처음 배양액 10l에 대한 총 효소량은 1,340kunits 단백질 양은 38,500mg였으며, 최종정제 단계인 Sephadex G-200에서는 총 효소 활성량은 421 kunits, 단백질량은 172mg이었으며 비활성은 약 70배로 증가했다.

• Clinical and Experimental Reproductive Medicine
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• 제26권2호
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• pp.137-148
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• 1999

Purpose of the present study was to find the optimal ovulation induction medicine for the maturation and development of immature oocytes and culture media for 2-cell embryos in the mouse model. ICR female mouse aged 6 to 8 weeks, were stimulated with 5 IU PMSG injection. At 47 to 50 hour post-PMSG injection, ovaries were dissected out and oocytes-cumulus complexes were punctured. The oocyte-cumulus complexes were cultured in media containing various ovulation induction medicine, CC, HMG and Metrodin for 18 hours. Female ICR mice were stimulated with 5 IU PMSG and 48 hours later were injected 5 IU of hCG, then female and male mice were mated. At 48 hour post-hCG injection, oviducts were dissected out and 2-cell embryos were flushed. The 2-cell embryos were cultured in various media, Ham's F-10 media of milli-Q water $(3^{\circ})$, Ham's F-10 media of HPLC (high performance liquid chromatography, Baxter) water, Medicult media, HTF (human tubal fluid) media for 96 hours. The results were as follows. 1. When the oocytes-cumulus complexes were cultured in $10^{-9}{\mu}g/ml{\sim}10^{-8}{\mu}g/ml$ of CC, those were suppressed in meiotic maturation $(28.2{\sim}33.7%)$. Whereas the oocytes-cumulus complexes were cultured in $10^{-7}{\mu}g/ml{\sim}10^{-4}{\mu}g/ml$, these were not effected in meiotic maturation $(54.5{\sim}72.7%)$. 2. When the oocytes-cumulus complexes were cultured in $10^{-4}{\mu}g/ml{\sim}10^{-1}{\mu}g/ml$ of Metrodin, those were suppressed in meiotic maturation $(35.7{\sim}41.5%)$. Meanwhile the oocytes-cumulus complexes were cultured in $10^{-7}{\mu}g/ml{\sim}10^{-5}{\mu}g/ml$, those were not effected in meiotic maturation $(54.2{\sim}70.3%)$. 3. When the oocytes-cumulus complexes were cultured in $10^{-5}{\mu}g/ml{\sim}10^{-4}{\mu}g/ml$ of HMG, those were suppressed in meiotic maturation $(48.2{\sim}50.4%)$. As being cultured in $10^{-7}{\mu}g/ml{\sim}10^{-6}{\mu}g/ml$, increased in meiotic maturation $(75.8{\sim}80.7%)$. 4. When the 2-cell embryos were cultured in Ham's F-10 media of milli-Q water $(3^{\circ})$, Ham's F-10 media of HPLC (high performance liquid chromatograpy, Baxter) water, Medicult media, HTF (human tubal fluid) media, developmental rates to blastocyst and hatching for 96 hour were 50.0%, 45.2%, 71.5% and 95.6%, respectively.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2003년도 생물공학의 동향(XII)
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• pp.209-212
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• 2003

본 연구는 고수율의 아라비녹실란을 얻기위해 필수요소인 Lentinus edodes의 액체배양을 통해 생산되어지는 탄수화물 복합효소의 생산수율을 증대시키는데 그 목적이 있다. 그러기 위해 탄수화물 복합효소의 생산에 배지성분이 미치는 영향을 검토 하였다.

• Journal of Microbiology
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• 제38권1호
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• pp.48-51
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• 2000

In liquid cultures using sucrose media, the coculture of Monascus with recombinant Saccharomyces cerevisiae expressing the glucoamylase gene from Aspergillus niger enhanced red pigment production by approx. 19％, compared with the coculture of wild type S. cerevisiae. Coculture with recombinant S. cerevisiae was more effective than with wild type S. cerevisiae for Monascus red pigment production. Cocultures of Monascus with commercial amylases of Aspergillus also induced high production of pigment and morphological changes in a solid culture using sucrose media.

• 한국자원식물학회지
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• 제11권2호
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• pp.176-176
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• 1998

This study was carried out to obtain the information for growth characteristics of crown gall tumor and hairy root transformed by Agrobacterium spp,. on the media with phytohormones, casein hydrolysate and activated charoal. Crown gall tumors and hairly roots were formed respectively on potato tuber discs infected by tumerfaciens A ch 5 and A.rhizogenes ATCC15834. These tumors and roots could be grown on the phytohormone free media. PCR analysis of Rol C and Vir C gene fragments confirmed that crown gall root was prompted on the medium containing 2,4-D 2mg/l with casein hydrolysate lg/l. The survival ration of crown gall tumor callus derived from potato increased on medium containing the activated charcoal 0.5∼0.2mg/l because of the prevention, on the other hand, hairly roots were necrosis on the same medium. Callus derived from hairly root were excellently grown for a short time by suspension culture on liquid medium containing 2.4-d 2mg/L and casein hydrolysate lg/l.

• 한국자원식물학회지
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• 제11권2호
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• pp.179-187
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• 1998

This study was carried out to obtain the information for growth characteristics of crown gall tumor and hairy root transformed by Agrobacterium spp,. on the media with phytohormones, casein hydrolysate and activated charoal. Crown gall tumors and hairly roots were formed respectively on potato tuber discs infected by tumerfaciens A ch 5 and A.rhizogenes ATCC15834. These tumors and roots could be grown on the phytohormone free media. PCR analysis of Rol C and Vir C gene fragments confirmed that crown gall root was prompted on the medium containing 2,4-D 2mg/l with casein hydrolysate lg/l. The survival ration of crown gall tumor callus derived from potato increased on medium containing the activated charcoal 0.5∼0.2mg/l because of the prevention, on the other hand, hairly roots were necrosis on the same medium. Callus derived from hairly root were excellently grown for a short time by suspension culture on liquid medium containing 2.4-d 2mg/L and casein hydrolysate lg/l.

• 한국식품위생안전성학회지
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• 제38권5호
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• pp.319-331
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• 2023

아미노글리코사이드계 항생제(Aminoglycosides, AGs)는 그람음성균과 양성균에 광범위하게 작용하는 동물용 의약품으로, 최근 배양육에 사용된다고 알려져 있어, 안전성 관리를 위한 분석법 마련이 반드시 필요하다. AGs는 고극성 화합물로 성분 간의 분리를 위해 이온쌍 시약(ion-pairing reagent, IPR)을 사용하고 있으나 IPR을 이동상에 첨가하는 기존 분석방법의 경우 용매가 흐르는 동안 질량분석기로 주입되는 IPR로 인해 기기적인 문제가 발생할 가능성이 높아, IPR를 바이알에 직접 첨가하는 분석방법을 검토하였다. 본 연구에서 10종 AGs 성분에 대한 분석방법을 확인하고 유효성을 검증하였다. 검출한계와 정량한계는 각각 0.0001-0.0038 mg/kg 와 0.004-0.011 mg/kg의 범위로 나타났으며, 0.01-0.5 mg/kg 범위 내의 직선성(R²)은 0.99 이상이었다. AGs의 시료 회수율을 확인하고자 소고기와 세포배양배지(cell culture medium) 매질에서 회수율과 상대표준편차로 나타낸 정밀도를 확인한 결과 각각 70.7-120.6% 및 0.2 to 24.7%로 나타났다. 기존의 이동상에 IP 첨가 방법과 비교하였을 때 유사한 수준으로 양호하였다. 검증된 AGs 분석법은 국내 유통되는 닭고기, 소고기, 돼지고기 15품목과 배양육 배지 첨가제 6품목에 적용해보았다. 그 결과 국내 유통되는 육류 15품목 모두 AGs 성분이 검출되지 않았으나, 세포배양배지에서 streptomycin은 695.85-1152.71 mg/kg, dehydrostreptomyci은 6.35-11.11 mg/kg로 검출되었다. 따라서 IRR을 바이알에 직접 첨가하는 LC-MS/MS 방식은 육류, 세포배양배지, 배지첨가제 중 AGs 분석 및 안전성 평가를 위한 기초자료로 활용될 것으로 기대된다.