• Journal of the Korea Academia-Industrial cooperation Society
• /
• v.9 no.3
• /
• pp.800-806
• /
• 2008

The strain HK-12 was enriched and isolated from naturally fermented soybean for the production of fibrinolytic enzyme and the proteome of this enzyme induced during the incubation period was analyzed. The activity of fibrinolytic enzyme derived from supernatants of the HK-12 culture was performed by fibrin plate method for solid fibrinolytic activity. As the result, the fibrinolytic activity of HK-12 grown on the nutrient agar media was about 2.3 times greater than that of plasmin used as standard. The purified enzyme was prepared by a series of purification process including ammonium sulfate precipitation, DEAE-cellulose, Sephadex chromatography. The molecular weight of the enzyme was determined to approximately 23kDa with SDS-PAGE. In order to examine which strain HK-12 proteins increased or decreased during the incubation period, 2-DE analysis was performed. Protein spot #1 significantly expressed on the 2-DE gel of bacteria cultivated for 36-hrs was analysed. As the result of protein sequence analysis using MALDI-TOF MS, one protein was identified as serine protein kinase (PrkA).

• Korean Journal of Agricultural Science
• /
• v.4 no.2
• /
• pp.239-253
• /
• 1977

In order to establish the effective method of producing calluses of Prunus persica, anthers were cultured on Nitsch's medium supplemented with combinations of several growth regulators. Anthers of tetrad stage were preserved in the refrigerator at $4^{\circ}C$ for 50~60 days. Calluses were embeded on the Murashige and Skoog's medium supplemented with multiplicate and differentiate the calluses. Changes of anther color, callus formation, and proliferation of haploid callus were observed under the different medium conditions. The results obtained were summarized as fellows: 1) The cultured anthers were turned dark brown 2~6days after were explanted anthers into the medium. 2) The anthers which were not changed in color were observed more frequently in the medium not added the growth regulators. 3) Calluses were induced from anthers which were turned dark brown and liberated from the anther slit. 4) BA. was very effective to induce calluses and to form the chlorophyll. The medium supplied with BA 0.5ppm were best to induce calluses. 5) The best medium supplied with BA 0.5ppm+IAA or 2.4-D were best to proliferation of calluses. 6) The medium was adjusted to pH 4.5 and supplied with 250mg/l of $CaCl_2{\cdot}2H_2O$ were induced calluses from anthers.

• Korean Journal of Ecology and Environment
• /
• v.42 no.3
• /
• pp.295-302
• /
• 2009

This study was conducted to identify the influences of light-to-nutrients ratio on the zooplankton and phytoplankton community. Various experiment conditions such as HL (high-light and without zooplankton), HLZ (high-light and with zooplankton), LL (low-light and without zooplankton), and LLZ (low-light and with zooplankton) were adjusted. Changes in biomass of phytoplankton species with the incubation time showed a similar tendency in the continuous cultures, but the change of species composition in the continuous cultures was detected. Cyanophyeeae (Phormidium sp.) seems to be affected by the existence of zooplankton. Also, the predominant species were Chlorophyceae (Staurastrum spp., S. dorsidentiferum, Coelastrum cambricam, Chlorella sp., Krichnerialla sp.) in a high-light environment and Bacillariophyceae (Melosyra granulata, Synedra acus, Fragilaria crotonensis) in a high-light environment. The estimated mean POC concentration (after twenty days) in a high-light environment was two times higher than that for a low-light environment. P : C ratio of seston component in a low-light environment was higher than that for a high-light environment. Changes in biomass of zooplankton species during the incubation time were higher than that for a high-light environment.

• Journal of Korean Society of Forest Science
• /
• v.23 no.1
• /
• pp.9-16
• /
• 1974

The anthers of late uninucleate microspore or early binucleate microspore stage of Paeonia suffruticosa Andr. (economic tree) were cultured on the modified Murashige and Skoog's medium suppliment with Keinetin, 2,4-D, and NAA for inducing haploid plants. The results are as follows; 1. Callus were induced from both anther locule and anther wall, where that from anther locule was identified as haploid. 2. Among 2,000 anthers cultured, fourteen haploid callus were developed. These haploid callus were clearly identified to be originated from the microspore in anther locule. 3. Diploid callus were induced only 0.5 percent from the callus of endothelium of anther wall, septium of two neighboring anther locule, parenchyma tissues of connectives and or anther locules. 4. In the anther locule of Paeonia suffruticosa Andr. cultured in medium, swollen microspores, polynucleate microspores, multicellurar pollen grains, or callus mass was frequently observed. And the haploids were seemed to be caused by the callus originated from the reduced microspore.

• 한국생물공학회:학술대회논문집
• /
• 2003.10a
• /
• pp.369-371
• /
• 2003

젤형 인공피부의 약한 물성을 보완하기 위해 스폰지형 인공피부가 개발되었으나 다공성 표면구조 때문에 세포의 배양이 어려운 문제점이 남아 있었다. 이 다공성 구조를 섬유모세포의 장기 배양으로 ECM으로 채우기 위해서는 3주이상의 긴 시간이 필요하며 그 위에 상피층 배양하기 위해서는 2주 이상의 시간이 추가로 소요되기 때문에 환자에게 이식할 적절한 시기를 놓칠수가 있다. 따라서 본 연구결과로 단기일 내에 전층 인공피부를 배양함으로서 적절한 이식시기를 맞출수가 있으며 이러한 기저막이 부착된 스폰지구조는 물성도 향상되어 이식시 조작이 쉽고 볼합이 가능한 장점이 있다.

• Proceedings of the Korean Society for Bio-Environment Control Conference
• /
• 2002.11a
• /
• pp.241-245
• /
• 2002

최근 시설재배에서는 염류 집적 및 토양전염성 병해충 등으로 인한 연작장해를 회피하기 위하여 수경재배로 전환하는 농가가 급속히 증가하고 있다. 우리나라의 수경재배면적은 '98년 23 ha에서 2000년 1,000 ha로 급속히 증가하고 있는데, 이중 약 12％는 담액수경이나 박막수경의 순수 수경재배 방식이 차지하고 있으나 대부분이 고형배지를 이용한 비순환방식이다. 배양액의 비순환방식은 토양이나 지하수의 오염이 염려되지만, 순환방식의 경우에는 배양액 성분의 조정이나 배양액의 소독 등재처리가 필요하여 농가에서는 기피하고 있는 실정이다. (중략)

• Korean Journal of Medicinal Crop Science
• /
• v.3 no.3
• /
• pp.233-239
• /
• 1995

The effects of media, growth regulators, low-temperature treatments, culture temperature and light were investigated to improve the callus induction and growth in the anther culture of Comus officinalis Sieb. et Zucco. The frequency of callus induction was more effective on WPM medium than MS medium, and it was highest as 54% in WPM medium supplemented with Img/L NAA. Callus growth was stimulated on MS medium supplemented with 2mg/L NAA. Effect of temperature and light on the callus induction and growth was highest as 62% in the treatment for 16/8 hrs. (light/dark) at $25^{\circ}C$ Ef­fect of low - temperature treatment on callus induction was highest as 19. 5% in the treatment for 36 hrs. at $4^{\circ}C$. For organization, green cells and rootings were promoted on MS medium supplemented with O. 5mg/L 2,4-D and 1 mg/L kinetin. The prevention of callus browning was effective on the medium con­taining $3{\sim}5mg/L$ ABA or 5mg/L $AgNO_3$. The supplement of ABA or $AgNO_3$,were maintained callus ac­tivity for 4-5 weeks and they were promoted the development of green cells.

• Microbiology and Biotechnology Letters
• /
• v.6 no.4
• /
• pp.187-196
• /
• 1978

Antimetabolite N-2292 substance, an antagonist of L-aspartic acid and L-glutamic acid was isolated from the fermentation broth of Streptomyces. Taxonomical study on the producing strain made it a related species of Streptomyces albulus judged by cultural characteristics and carbon utilization. N-2292 substance was isolated as amorphous white powder with melting point at 185$^{\circ}C$. From the physicochemical characteristics of the substance, it was peptide like substance. It was active against Gram positive and Gram negative bacteria but negative against yeast and mold in its biological properties. It was reversed by L-Asp and L-Glu on the synthetic medium.

• Korean Journal of Plant Tissue Culture
• /
• v.28 no.6
• /
• pp.335-339
• /
• 2001

Grapevine leafroll-associated 3 closterovirus (GLRaV-3) is phloem limited virus, and one of the most severe viral diseases found in Korea. However, nonhomogenous distribution and low concentration and seasonal variations of GLRaV-3 in grapevines remain as main problems which prevent the introduction and molecular biology or serology experiments. Virus-infected plantlet in vitro was obtained from node tissue cuttings, which was GLRaV-3 infected 'kyoho' vines. The amount of purified virus was highest in vitro plantlet. Moreover, viruses seem to be relatively homogeneously distributed in all organs including leaf, stem and callus derived from in vitro plantlets. RT-PCR detection using in vitro plantlet tissue as template was most effective. When comparing ELISA to RT-PCR, RT-PCR detection was 1,000 times as effective as ELISA. These results can be explained by improved quality such as tenderness or less tannins in plantlet in vitro. In conclusion, until infected herbaceous host will be available, tissue culture can be usefully adopted as a technique for a good source of GLRaV-3 closterovirus for further studies.

• Microbiology and Biotechnology Letters
• /
• v.32 no.1
• /
• pp.52-59
• /
• 2004

When both fructose and galactose were added to a production medium as carbon sources, the productivity of PAFS (Psedomonas Antifungal Substance) biosynthesized by Pseudomonas aeruginosa was observed to be reduced significantly due to the well-known phenomenon of catabolite repression. In order to overcome this phenomenon by use of fermentation bioprocess, fed-batch cultivation method was examined. In addition, a high producer mutant strain, AP-20 obtained by a rational screening method was tested for its productivity of PAFS in both batch and fed-batch fermentation processes. Notably fed-batch operation showed approximately 4 fold higher PAFS productivity than traditional batch operation process. It was appeared that galactose was utilized principally for the cell growth of Pseudomonas aeruginosa whereas large portion of fructose was used for the biosynthesis of PAFS. Furthermore it was observed that composition and feeding rate of production media should be optimized even in the fed-batch fermentation bioprocess. As an example, very slow feeding of carbon sources gave rather negative effect on the production of PAFS due to significant limitation of carbon and energy sources available for the producer microorganism.