• 미생물학회지
• /
• 제22권1호
• /
• pp.49-56
• /
• 1984

Novozym 234에 의한 K. fragilis와 C. pseudotropicalis의 원형질체 형성과 재생에 관한 연구를 하였다. intact cell을 원형질체로 전환시키는데 정지기의 세포보다 대수기에 있는세포가 효과적이었으며 osmotic stabilizer로는 $(NH_4)_{2}SO_4$가 두 종 똑같이 원형질체 형성이나 재생에 있어서 적합했고 최적 효소농도는 K. Fragilis에서는 3mg/ml, C. pseudotropicalis에서는 1~3mg/ml이었다. 반응 후 관찰된 세포 중의 원형질체 형성 수율은 K. fragilis에서 약 95%, C. pseudotropicalis에서 약 100%였으나 원형질체의 재생은 Glusulase와 비교해 볼 때 매우 낮았다. 그러나 세포 이물질이 없는 원형질체를 얻는데는 Novozym 234가 적합한 것 같다.

• 한국균학회지
• /
• 제22권2호
• /
• pp.130-137
• /
• 1994

담자균류인 잿빛 만가닥버섯 Lyophyllum decastes은 이미 항암작용이 있다고 보고된 바, 이 버섯의 유전연구와 균주개발을 위해 기초적 연구인 원형질체 분리와 재생에 관하여 실험하였다. 원형질체 분리의 최적 조건으로는 여러 효소의 혼용보다 Novozym 234(10 mg/ml)를 단용하였을 때 더 우수하였고, 삼투압 안정제로 0.6 M $MgSO_4$에서 효과적이었으며, $24^{\circ}C$ 에서 5일 배양한 균사와 효소액을 4시간 반응 시켰을 때 수득율이 높았다. 완충용액과 pH는 Na-phosphate buffer(pH 4)에서 원형질체 분리가 양호 하였으며, 고체배지보다 액체배지에서 자란 균사를 완충용액과 pH를 조절하지 않은 상태에서 효소와 반응시켰을 때 $12.5{\times}10^6\;cell/ml$로 높았다. 원형질체 재생시 균사가 배지 전면에 확산되어 성장하여 성장억제제로 Triton X-100(0.0025%)을 사용하였다. 원형질체 분리시와는 대조적으로 0.6M sucrose와 mannitol에서 재생이 효율적이었고, 각각 8.32%와 5.94%의 재생 빈도를 나타내었다.

• 한국균학회지
• /
• 제14권2호
• /
• pp.141-148
• /
• 1986

버섯의 품종개발(品種開發)과 유전연구(遺傳硏究)를 위해서 느타리 균(菌)의 일종(一種)인 P.cornucopiae 노랑 느타리의 원형질체(原形質體) 분리(分離)에 적합한 제조건(諸條件)을 조사하였다. 원형질체(原形質體) 분리(分離)의 최적(最適) 조건(條件)으로 Novozym 234농도(濃度)는 $5\;mg{\cdot}ml^{-1}$이었고 Novozym $234+{\beta}-D-glucanase\;+{\beta}-glucuronidase\;mixture$에서 원형질체수(原形質體數)는 $10.55{\times}10^6\;ml^{-1}$으로 가장 높았으며, 삼투압(渗透壓) 조절제(調節劑)와 농도(濃度)는 0.6 M sucrose에서 효과적(效果的)이었고 혼합효소액(混合酵素液)과의 반응(反應) 90분일때 원형질체(原形質體) 분리량(分離量)은 $2.2{\times}10^7\;ml^{-1}$으로 높았다. 완충용액(緩衝溶液)과 pH는 0.6 M sucrose+Na-maleate buffer (pH 5.0), 0.6 M sucrose+phosphate buffer(pH 6.2)에서 원형질체(原形質體) 분리량(分離量)이 좋았으며 대체로 phosphate buffer가 효과적인 것으로 나타났고 pH를 조절하지 않은 0.6M sucrose 삼투압 조절제(調節劑)가 원형질체(原形質體) 분리(分離)에 가장 알맞았다. 그리고 배양(培養) 일수(日數) 및 균사체량(菌絲體量)을 보면 cellophane MCM에서 4일 배양(培養)한 균사체(菌絲體) 6colonies와 혼합효소(混合酵素) 4 ml과 혼합하여 $28^{\circ}C$에서 90 분간 흔들었을 때 원형질체(原形質體)가 가장 많이 분리되었다.

• 미생물학회지
• /
• 제23권3호
• /
• pp.209-214
• /
• 1985

The optimum conditions of protoplasts formation from Pyricularia oryzae were investigated with lytic enzymes and osmotic stabilizers. The mycelia were begun to refease the protoplasts in response to the complex enzyme solution after 30-60 minutes and reached to maximum after 2-3hrs. Among the lytic enzymes tested, the mixture solution containing ${\beta}-Glucuronidase$(0.01 ml/ml), Cellulase ONOZUKA-RS(20mg/ml), Driselase (10mg/ml), and Macerozyme R-10 (10mg/ml) resulted in the highest rate of protoplasts releasing of Pyricularia oryzae. The best stabilizer was 0.6M KCl at pH 7.0. Shen the mycelia were digested with enzyme mixture, the stationary culture was better than shaking culture for higher protoplast formation.

• 미생물학회지
• /
• 제29권2호
• /
• pp.123-129
• /
• 1991

In order to develop the protoplast fusion method of the strains of Fusarium, the interspecific protoplast fusion was attempted between Fusarium poae and F. sporotrichioides. Various auxotrophic mutants were isolated by the treatment of N-Methyl-N'-Nitro-N-Nitrosoguanidine. The optimal conditions for the formation and regeneration of protoplasts were examined and the characteristics of a fusant were studied. As a results, protoplasts were readily obtained from 18 hours cultured mycelia by the treatment of driselase for 3 hours and 0.6 M KCl as a best osmotic stabilizer at pH 6.0 for the formation of protoplast. Sucrose was the most suitable for the regeneration. Polyetylene glycol (M.W. 8,000) in $CaCl_{2}$-glycine solution was used to induce the protoplast fusion. The interspecific fusion frequency between protoplasts among the auxotrophic mutants of the two strains ranged from $2.7*10^{-2}$ to $5.7*10^{-3}$ . DNA content and cellulase activity were rather increased in the interspecific fusant. The lag phase of growth curve was slightly elongated in the fusant.

• 한국미생물생명공학회:학술대회논문집
• /
• 한국미생물생명공학회 1986년도 추계학술대회
• /
• pp.527.3-527
• /
• 1986

Several factors predicted to affect the protoplast formation and regeneration were investigated. The optimum lysozyme, casamino acid and PVP concentration were 0.5 (mg/$m\ell$), 0.1 (%) and 1.5(%). In B. pumilus, Penicillin-G treatment concentration was 0.3 (U/$m\ell$) and optimum treatment period was transit log. phase. And in the case of Celm. fimi, 0.3 (U/$m\ell$) and initial log. phase. Osmotic stabilizer and di-cation for OSM medium of B.pumilus and Gelm .fimi were 25mM CaCl2, 0.5M sodium sucinate and 50mM MgCl$_2$, 100mM CaCl$_2$, 0.4M sodium succinate. The regeneration frequency of B.pumilus and Celm. fimi were 14.6(%) and 6.9(%).

• Geomechanics and Engineering
• /
• 제15권4호
• /
• pp.957-964
• /
• 2018

In this study, a method of electrochemical consolidation is applied. This method utilizes electro-osmosis, which is an effective ground improvement technique for soft clays, and soil treatment using lime, which is the oldest traditional soil stabilizer. The mechanism of lime treatment for soil involves cation exchange, which leads to the flocculation and agglomeration. Five representative laboratory tests-an electro-osmotic test and four electrochemical tests with various proportions of lime-were performed on dredged marine clay. The objectives of this study are to investigate the effect of electrochemical treatment and to determine the optimum dose for optimal consolidation performance of dredged marine clay. The results show that a better consolidation effect was achieved in terms of current, temperature, and vane shear strength by using electrochemical treatment. The best results were observed for the electrochemical test using 4% lime content.

• 미생물학회지
• /
• 제24권2호
• /
• pp.91-97
• /
• 1986

Intra and interspecfic fusants were produced by the protoplast fusion of auxotrophic mutants from Trichoderma koningii ATCC 26113 and Trichoderma reesei QM 9414. It was found that 0.6M $MgSO_4\;and\;0.6M\;NH_4Cl$ was the best osmotic stabilizer for the preparation of protoplasts from the mycelium of T. koningii and T. reesei respectively. However, $MgSO_4$ was the most suitable one for the regeneration of the protoplasts from both species. The intraspecific protoplast fusion frequencies between the auxotrophic mutants from T. reesei were $1.8{\times}10^{-2}\;to\;5.1{\times}10^{-1}$. Interspecific protoplast fusion frequencies between the auxotrophic mutants from T. koningii and T. reesei were $3.6{\times}10^{-3}$\;to\;8.4{\times}10^{-2}. Interspecific complementing fusants, however, were not alwats produced. Fusants obtained from interspecific potoplast fusion were spontaneously segregated into various strains including parental types, non-parental auxotrophic hybrids, and prototrophic hybrids on complete plate. Interspecific hybrids revealed to have partially enhanced celluloytic activities.

• KSBB Journal
• /
• 제13권4호
• /
• pp.399-403
• /
• 1998

This study was carried out to optimize the concentration of Ca2+ and pH of fusion medium which affected electrofusion frequency of protoplasts isolated from Nicotiana tabacum L. (cv. BY4) mesophyll cells and callus. The protoplasts were electrofused in the fusion media containing two different Ca2+ concentrations and three different pH regions. Fusion frequency was lower in the fusion medium containing only 13% mannitol as osmotic stabilizer. However, higher degree of fusion frequency (47.3%) was observed in the fusion medium containing 50mM CaCl2 at pH 10.5 than any other conditions. Cell viability was decreased by Ca2+ and high pH treatment in the fusion media, while fusion frequency was increased. It is concluded that Ca2+ is involved in electrofusion of protoplasts.

• 한국미생물·생명공학회지
• /
• 제23권3호
• /
• pp.359-364
• /
• 1995

Two lactic strains, Leuconostoc mesenteroides Lu5 and Pediococcus pentosaceus P1 isolated from Kimchi, were used to determine the optimum conditions for protoplast formation and regeneration. The maximum protoplast formation rate was obtained with both strains at early exponential growth phase and decreased rapidly during growth phase. For P. pentosaceus P1, 30 $\mu$g/ml of lysozyme treatment was sufficient to obtain over 90% of protoplast formation and 300 $\mu$g/ml for L. mesenteroides Lu5, showing great difference in sensitivity of these strains to lysozyme. For both strains, best results were obtained at pH 7, using 0.5 M sucrose as osmotic stabilizer. For regeneration of protoplast, the highest regeneration rate was obtained after 15 minutes of lysozyme treatment and declined drastically with prolonged digestion.