• 한국해양바이오학회지
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• 제11권2호
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• pp.71-80
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• 2019

Previously, agar obtained from Gelidum sp. has a small molecular weight and has the disadvantage of inherent viscosity properties and poor functionality as a dietary fiber. In order to improve aforementioned disadvantages, agar having a fluidity that can be added to food at a higher concentration that a powder agar having a gelling property at low concertation was manufactured. In addition, the anti-inflammatory activity of agar hydrolysates was evaluated to confirm their potential as a functional material. As a result, agar hydrolysates significantly reduced NO levels secreted by LPS-activated macrophages and inhibited the expression of iNOS and COX-2, which are inflammatory mediators that regulates NO secretion in macrophages. Furthermore, in in vivo zebrafish embryos model results demonstrated significant reduction of LPS induced NO production after the treatment of agar hydrolysate hydrolyzed for 360 min. In addition, ROS production and cell death by stresses were also reduced in LPS-exposed embryos after the treatment of agar hydrolysis product hydrolyzed for 360 min. Taken together, agar hydrolysate hydrolyzed for 360 min can be easily added into food due to their fluidity and used as a food ingredient that inhibits inflammation due to their anti-inflammatory property.

• KSBB Journal
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• 제13권4호
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• pp.378-382
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• 1998

Agar hydorlysates or agarooligosaccharides from agar prepared by Cytophaga agarase showed eight spots on TLC plate and the degree of polymerization of the spots were in the reange of 2.5 - 6.5. Each component of the hydrolysate as tested the several functionalities such as antimicrobial activity, anticavity activity, and anticoagulant activity. The anticativity activity and anticoagulant acitvity were found in all fractions of hydrolysates and several spot on TLC, whereas the anticoagulant activity was very low.

• Journal of Microbiology
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• 제39권1호
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• pp.17-23
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• 2001

Various pretreatment procedures and selective media were applied to assess the optimal conditions for the isolation of rare actinomycetes from soil. Pretreatment of wet-heating for 15 min at 70$^{\circ}C$ and phenol treatment of soil suspension were the most effective methods for the isolation of these microorganisms. Hair hydrolysate vitamin agar (HHVA) was the most suitable medium for the recovery of rare actinomycetes. Thirty-five rare actinomycete strains were chosen using selective isolation approaches, then morphological and chemical properties of the isolates were determined. The isolates belonged to one of the following genus, Micromonospora, Microbispora, Actinoplanes and Streptosporangium.

• 한국미생물·생명공학회지
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• 제22권5호
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• pp.561-563
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• 1994

For the more effective isolation of soil actinomycetes, we have developed HHV (Hair hydrolysate-vitamin) agar medium, containing hair as the sole source of carbon and nitrogen. The HHV agar medium was superior to other media such as colloidal chintin agar, glycerol-arginine agar and starch-casein-nitrate agar, and HV (humic acid-vitamin) agar. The maximum effect of this medium has been shown in hair dry weight 0.4 g/l medium. Of each soil sample, the greatestest number of actinomycetes was isolated from the potato annual planted soil among the tested samp- les. The genus of actinomycetes isolated from the potato annual planted soil sample was identified such 5 group as Stretomyces, Micromonospora, Microbispora, Nocardia and Saccharopolyspora.

• 한국식품영양학회지
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• 제10권4호
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• pp.528-532
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• 1997

새조개 여체부의 긴발을 제외한 나머지인 가공 부산물을 식량자원으로서 효율적 이용을 위한 한 방안으로 효소분해 후 가수분해물의 물성을 개선하여 다소의 조직감을 갖는 반고형 상태의 페이스트 젓갈의 제조와 품질개선에 관하여 검토하였다. 새조개 가공부산물에 절반량의 물과 4% Protease N. P.를 첨가하여 가수분해 후 여과하여 그 여액에 4% glucose를 첨가하여 10$0^{\circ}C$에서1시간 열처리하여 풍미개선, 효소의 불활성화 및 멸균을 시켰다. 물성개량제 즉 0.5% alginic acid, 1% pectin, 0.2% agar를 병용 첨가한 제품이 대조구에 비하여 조직감 및 물성개선의 효과를 나타내었고, 10,000 rpm에서 60분간 원심분리 후에도 조직감이 파괴되지 않아 그 때의 혼합안정성은 98.1%였다. 페이스트 젓갈의 성분은 수분 함량 57.7%, 총당 함량 20.6%, 총질소함향 1,458% 및 아미노질소량 1,187mg%이었으며, 총질소중 아미노질소가 차지하는 비율은 81.4%였다.

• 한국수산과학회지
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• 제30권1호
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• pp.79-87
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• 1997

A study on the processing method of anchovy hydrolysate paste (AHP) was carried out to improve the sensory quality of salted and fermented fish. Homogenized whole anchovy was hydrolyzed using commercial pretenses, Complex enzyme-2000 (CE, Pacific Chem. Co.) and Alcalase (AL, Novo), in a cylindrical vessel with 4 baffle plates and 6-bladed turbine impeller. Optimal pH, temperature, and enzyme concentration for the hydrolysis with CE and AL were $7.0,\;52^{\circ}C,\;7\%$, and $8.0,\;60^{\circ}C,\;6\%$, respectively. The rational amount of water for homogenization, agitation speed, and hydrolyzing time were $100\%\;(w/w)$, 100 rpm, and 210 min, respectively. To make the hydrolysate to paste type, it was effective to mix the additives, such as starch, soybean protein, agar, and carrageenan gum to the hydrolysate 5 min before the end of boiling at $100^{\circ}C$ for 30 min. Minimal NaCl concentration for long-term preservation was $15\%$, and this could be reduced to $12\%$ by adding $5\%$ of KCl. yield of the AHP based on the total nitrogen content was $94.6\~97.0\%,\;and\;86.0\~89.2\%$, of the nitrogen was amino nitrogen. Salinity, pH and histamine content of the AHP prepared with $12\%$ NaCl and $5\%$ KCl were $9.3\~9.9\%,\;6.1\~6.2$, and below 13 mg/100 g, respectively. The AHP was stable at $26{\pm}3^{\circ}C$ for 60 days on bacterial growth, and addition of $0.05\%$ of rosemary (Herbalox) extract was effective to inhibit the lipid oxidation of the AHP during storage.

• 공업화학
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• 제23권3호
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• pp.279-283
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• 2012

화석연료로 인한 환경오염 등의 문제를 해결하기 위해서 다양한 원료를 이용하여 바이오 에탄올 생산에 대한 연구가 진행되고 있다. 해조류 중에 홍조류는 agar, carrageenan, porphyran으로 구성되어 있어 산 처리를 통해 바이오에탄올 생산에 유용한 바이오매스로 전환이 가능하다. 본 연구는 홍조류의 가수분해물을 이용하여 바이오에탄올 생산의 최적 조건을 찾으려고 한다. 바이오에탄올 생산하기 위해 전처리 된 우뭇가사리에 Saccharomyces cerevisiae KCCM112를 접종해 발효하였다. 우뭇가사리 가수분해의 최적조건은 1.5% $H_2SO_4$를 $121^{\circ}C$에서 30 min 반응시켰을 때 7.04 g/L의 galactose와 1.94 g/L의 glucose가 생산되었다. 그리고 $CH_3COOH$의 경우 2.0% 농도로 처리하였을 때, galactose 0.75 g/L가 생산되었다. 이와 반대로 도박에서는 $H_2SO_4$1.5%를 처리하였을 때 galactose를 6.38 g/L 생산하였으며, $CH_3COOH$을 처리했을 때 0.368 g/L이 생산되었다. 우뭇가사리에서 에탄올 생산은 1.0% $H_2SO_4$를 $121^{\circ}C$에서 30 min 간 처리하였을때 가장 높았으며, 96 h 배양하였을 때 3.77 g/L의 에탄올을 생산했다.

• 한국수산과학회지
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• 제27권5호
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• pp.509-514
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• 1994

키조개 부산물을 이용하여 속성 젓갈화를 시도하였다. 마쇄한 키조개부산물에 Protin P $5\%$를 가하여 pH 7.0, $55^{\circ}C$에서 1시간 동안 가수분해시킨 후 불활성화를 위하여 $100^{\circ}C$에서 40분간 열처리시키되, 풍미를 개선하기 위하여 $10\%$의 invert sugar를 첨가하였다. 또한 제품의 물성개선을 위하여 PGDG을 $8\%$ 가하여 유화시킨 후 $2\%$의 한천과 $6\%$의 전분을 함께 첨가하여 조직감을 갖는 반고형 상태로 하고 최종적으로 식염농도를 $15\%$로 조절하였다. 시료로 사용한 키조개부산물은 패주를 제외한 나머지 부분으로 전내용고형물 중량의 $51.6\%$를 차지하였다. 풍미개선을 위하여 $10\%$의 invert sugar를 첨가하여 열처리한 것이 비린내와 쓴맛을 억제시켰다. 또한 한천 $2\%$ 및 전분 $6\%$의 첨가는 대조구에 비하여 hardness, springiness 및 chewiness를 개선시키는 효과를 보였다. 그리고 $23{\pm}3^{\circ}C$에서 저장하였을 때 생균수는 60일째까지 검출되지 않았다. 키조개부산물로 제조한 젓갈중의 주요 아미노산들로는 Glu, Arg, Asp, Leu, Lys, Gly 및 Ala 순으로, 전체 유리아미노산 함량의 $60\%$ 이상을 차지하였고, 저장 90일후에도 양적순서와 함량이 크게 변하지 않았다.

• Journal of Plant Biology
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• 제36권3호
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• pp.211-218
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• 1993

Plant regeneration was accomplished from protoplast culture of rice (Oryza sativa L. cv. Taebaeg). Embryogenic callus was induced from mature seed on MS medium containing 5 mM proline, 2.5 mg/L 2,4-D, 30 g/L sucrose in the dark at 28$^{\circ}C$ and used to establish embryogenic cell suspension culture. Suspension cells were subcultured every one week in N6 medium supplemented with 5 mM proline, 200 mg/L casein hydrolysate, 2.5 mg/L 2,4-D and amino acids of AA medium. Suspension cultures were composed of cells that were densely cytoplasmic, potentially embryogenic and were at least maintained for more than 6 months in liquid medium. Protoplasts were isolated from fast-growing suspension culture cells and cultured in a slightly modified KpR medium by mixed nurse culture. Isolated protoplasts began to divide within 5~7 days and thereafter, protoplast-derived calli were sequentially transferred to callus proliferating medium that soft agar MS medium contained 2 mg/L 2,4-D and produced distinct embryogenic cells. Microcolonies were then transferred to solid medium which consisted of MS medium containing 5 mg/L kinetin, 1 mg/L NAA, 1 mg/L ABA, 30 g/L sucrose and 10 g/L sorbitol under fluorescent light. Mulitple shoots of 4~5 per callus emerged and were transferred to hormone-free MS medium for root initiation. Thereafter, The plantlets were transferred to pots of soil to mature in the culture room.

• 식물조직배양학회지
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• 제24권3호
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• pp.183-188
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• 1997

본 시험은 L. longiflorum 'Gelia'의 캘러스 유지 및 증식, 캘러스 선발, 액체현탁배양 등의 단계로 수행하였다. 재분화를 억제시키면서 캘러스를 유지 증식시키기 위하여 MSH배지에 2.4-D 0.5 mg/L , NAA 1.0 mg/L, BA 0.3 mg/L를 첨가한 배지가 가장 효과적이었으며 재분화를 억제시키기 위해 2,4-D의 첨가는 필수적이었다. 당은 30 g/L 첨가가 캘러스 생육에 가장 적합하였고 50 g/L 이상 고농도는 캘러스 생육에 억제적이었다. 또한 0.42%의 한천을 첨가한 반고형배지에서 캘러스의 생육이 증진되었다. 4~5회 계대배양된 캘러스에서 유사배발생 캘러스(ELC)가 관찰되었다. ELC의 증식과 캘러스의 유연성을 증진시키기 위해 $\textrm{NO}_{3^-}$ 와 $\textrm{NH}_{4^+}$의 비율을 달리하여 배양한 결과, 전반적으로 NO$_3$-의 함량이 높은 배지에서 배양된 캘러스는 생육과 유연성이 양호하였다. 그러나 체세포배발생 가능성이 있는 캘러스의 증식에는 효과적이지 못했다. 액체배양은 MSH배지에 NAA 1.0 mg/L, BA 0.3 mg/L, 16.7% conditioned배지(30 mL당 1 mL), casein hydrolysate 2.0g/L를 첨가한 액체배지에 배지 30 mL당 1.5 g의 캘러스를 배양했을때 가장 캘러스 증식효율이 높았다. 광학현미경으로 조직을 관찰한 결과 1년 이상 장기배양된 캘러스에서 기관분화가 가능했고 배발생 초기단계의 세포도 관찰되어 백합 'Gelia' 캘러스로부터 체세포배 형성이 가능함을 알 수 있었다.