• 한국약용작물학회지
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• 제8권4호
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• pp.351-361
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• 2000

알콜 발효 증진을 위해 5L 배양조에서 혐기적으로 회분 배양 시 건지황 착즙액을 농도별로 첨가하며 알콜 발효 및 균체 생육을 측정한 결과 균체 생육 및 알콜 생산 수율 모두 착즙액 첨가량이 증가함에 따라 일반 발효에 비해 증가했으며, 30% (v/v) 첨가 시 11.8 (g/L)의 최대 균체양, 0.092 (%/hr)의 최대 알콜 생산성과 같은 최대치를 나타냈다. 하지만 40% 이상 첨가 시는 균체 생육 및 알콜 생산 두 경우 다 감소하는 경향을 보였으며 50% 에서는 심각한 생육 저해 현상이 나타났다. 또한 알콜 생산성 증진을 위해 30% 착즙액을 첨가해 유가식 배양을 실시 한 결과 회분 배양보다 월등히 높은 균체 생육 및 알콜 생산성을 보였다. 이 같은 생산성은 일반 알콜 발효에서 얻을 수 있는 수율보다 약 30-40% 이상 높은 것으로 건지황 착즙액이 알콜 발효에 직접적인 영향을 주는 것이 입증되었다. 이는 알콜 발효 시 건지황의 유용 성분의 활용과 함께 알콜 생산 수율 증진에도 이용이 가능한 지황의 이중적 활용도가 있음을 입증한 것으로 평가된다.

• Journal of Ginseng Research
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• 제38권1호
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• pp.52-58
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• 2014

To determine whether Fourier transform (FT)-IR spectral analysis combined with multivariate analysis of whole-cell extracts from ginseng leaves can be applied as a high-throughput discrimination system of cultivation ages and cultivars, a total of total 480 leaf samples belonging to 12 categories corresponding to four different cultivars (Yunpung, Kumpung, Chunpung, and an open-pollinated variety) and three different cultivation ages (1 yr, 2 yr, and 3 yr) were subjected to FT-IR. The spectral data were analyzed by principal component analysis and partial least squares-discriminant analysis. A dendrogram based on hierarchical clustering analysis of the FT-IR spectral data on ginseng leaves showed that leaf samples were initially segregated into three groups in a cultivation age-dependent manner. Then, within the same cultivation age group, leaf samples were clustered into four subgroups in a cultivar-dependent manner. The overall prediction accuracy for discrimination of cultivars and cultivation ages was 94.8% in a cross-validation test. These results clearly show that the FT-IR spectra combined with multivariate analysis from ginseng leaves can be applied as an alternative tool for discriminating of ginseng cultivars and cultivation ages. Therefore, we suggest that this result could be used as a rapid and reliable F1 hybrid seed-screening tool for accelerating the conventional breeding of ginseng.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2003년도 생물공학의 동향(XII)
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• pp.236-239
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• 2003

생물반응기를 이용한 회분배양에서 균체량 생산에 있어서 조건은 200 rpm, 1 vvm 으로 선정하였으며, 이때 균체량은 11 g/L이었고, polysaccharide는 0.6 g/L이었다. 또한 pH를 초기 pH인 5.5로 고정하여 배양한 결과 pigment들로 인한 균사체의 활성이 떨어지는 것으로 나타났다 균체량을 증가시키기 위한 최적의 회분배양 조건에서는 초기 200 rpm으로 배양을 시작하여 300 rpm으로 증가시키고 glucose 5 g/L를 간헐적으로 첨가함으로써 균체량은 24.2 g/L, polysaccharide는 2.2 g/L로 나타났다. 또한 erinacine A의 분석은 HPLC를 사용하였으며 배양 4.5일째 균사체로부터 추출하여 mobile phase를 Methanol/water (9:1)로 flow rate은 0.7 ml/min으로 실험한 결과 erinacine A는 0.4 mg/g cell 로 측정되었다.

• Journal of Microbiology and Biotechnology
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• 제1권2호
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• pp.111-115
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• 1991

The green alga, Dunaliella salina under fed-batch cultivation produced 51.12 mg of hydrocarbon per liter with maintaining 0.313 (g dry wt/l). About 20% of hydrocarbon production yield based on dry biomass was obtained from both batch and fed-batch processes. Optimum culture conditions of light intensity, pH and salt concentration were obtained as 0.0080 (kJ/$cm^2$/h), 8.0 and 1.4 (g of NaCl/l), respectively by response surface analysis. The production of hydrocarbons in D. salina was closely correlated to cell growth. Fed-batch cultivation produced more hydrocarbons and maintained better cell growth than a batch process.

• 한국식품영양학회지
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• 제1권2호
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• pp.43-49
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• 1988

Fermented barley food was produced by the combining action of an enzyme and a lactobacillus. When Lactobacillus sp. L-5 and commercial liquefying amylase from Tae Pyeong Yang Chemical Co. were selected, inoculated on steamed barley and cultivated at 37$^{\circ}C$ for 48hrs, the fermented product of good quality was obtained. In batch cultivation using rotary drum fermentor, viable cell count reached 1.1$\times$10CFU/g after 12hrs' cultivation, and specific growth rate in logarithmic phase was 0.6hr-1. Viable cell count, acidity, pH, concentration of reducing sugar and viscosity of the 48hrs' fermentation product from rotary drum fermentor was 4.3$\times$108CFU/g, 1.17%, 3.1, 10.7% and 1430cp.

• Journal of Microbiology and Biotechnology
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• 제12권3호
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• pp.457-462
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• 2002

Low Electromagnetic Field (EMF) intensity in the range of $1{\mu}T\;to\;10{\mu}T$(Tesla) was found to enhance the growth of CHO cells and the production of tPA in batch and perfusion cultivations. At $1{\mu}T\;intensity,\;1.3{\times}10^7$ viable cells/ml of maximum cell density and 80 mg/l of maximum tPA production were obtained in batch cultivation, compared to $2.8{\times}10^6$ viable cells/ml and 59 mg tPA/1 in unexposed case (control). A similar trend was observed in the perfusion process, where it was possible to obtain $1.2{\times}10^7$ viable cells/ml of maximum cell density and 81 mg tPA/l of maximum tPA production by more than 80 days of cultivation. However, there was not much difference between $1{\mu}T\;and\;10{\mu}T$ in perfusion cultivation, possibly due to better environmental growth conditions being maintained by continuous feeding of fresh medium into the reactor. On the contrary, both cell growth and tPA production were severely inhibited at higher than 1 mT intensity, showing no growth at 10 mT exposure. Specific growth rate was linearly correlated to specific tPA production rate at $1{\mu}T$EMF intensity, which represents a partially growth-related relationship. It was also found that a large amount of $Ca^2+$ was released at low EMF intensity, even though the cell growth was not much affected. Low EMF intensity significantly improved both cell growth and tPA production, and tPA production seemed to be more affected than the cell growth, possibly due to the changes of cell membrane characteristics. It can be concluded that the elaboration of EMF intensity less than $10{\mu}T$ could improve cell growth and tPA production, but mainly tPA secretion through batch or perfusion process in a bioreactor.

• 생약학회지
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• 제2권4호
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• pp.177-179
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• 1971

The study on cytotoxicities of domestic antitumour crude drugs were carried out in order to evaluate the antitumour activity. The eleven crude drugs were studied in this paper. No cytotoxicities were observed both at 0.1ml of water extracts and alcohol extracts deuted against monkey kidney cell and HeLa-cell after 3 days cultivation at $37^{\circ}C$. The sample shown the heavy cytotoxicities against monkey kidney cell at 0.3ml alcohol extracts diluted sample solution are Lonicerae Flos and Puchrestae Radix.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2000년도 춘계학술발표대회
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• pp.223-226
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• 2000

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2005년도 생물공학의 동향(XVI)
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• pp.198-198
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• 2005

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2000년도 추계학술발표대회 및 bio-venture fair
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• pp.676-679
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• 2000