• 미생물학회지
• /
• 제22권3호
• /
• pp.175-181
• /
• 1984

In order to develope a protoplast fusion system for industrial coryneform bacteria, the optimum conditions for the formation and regeneration of progoplast were examined for Brevibacterium flavum and Corynebacterium glutamicum and the protoplast fusion was performed. For the formation of the protoplast of B. flavum and C. glutamicum, the optimum time for penicillin G. treatment to obtain protoplast was mid-exponential growth phase ($O.D_{580}=0.6-0.8,\;8.0{\times}10^7-1.0{\times}10^8cell/ml$). At the optimum conditions (0.3units/ml penicillin G and $400{\mu}g/ml$ lysoyme for treatement), frequencies of protoplast formation and protoplast regeneration were 99% and 25%, respectively. Protoplast regeneration frequency was highest under the optimum conditions for the protoplast formation. Addition of 25mM $Mg^{2+}\;and\;50mM\;Ca^{2+}$ to the regeneration medium further increased the regeneration frequencies. The protoplast fusion frequencies of B. flavum and C. glutamicum in intraspecies fusion were $1.0{\times}10^{-8}\;and\;7.8{\times}10^{-4}$, of the regenerated protoplast respectively, when 33% of PEG (polythylene glycol) 6,000 was used as the fusing agent.

• Mycobiology
• /
• 제47권4호
• /
• pp.483-493
• /
• 2019

Antrodia cinnamomea is a unique medicinal fungus in Taiwan. It has been found rich in some pharmacologically active compounds for anti-cancer, hangover, and immune regulation etc. With the in-depth study of these components, it would be interesting and important to establish a molecular system for basic studies of A. cinnamomea. Thus, we would like to set up a foundation for this purpose by studying the A. cinnamomea protoplast preparation and regeneration. Firstly, we studied the optimization method of protoplast preparation of A. cinnamomea, and found various factors that may affect the yield during protoplast preparation, such as mycelial ages, pH values, and osmotic stabilizers. Secondly, in the regeneration of protoplasts, we explored the effects of various conditions on the regeneration of protoplasts, including different media and osmotic pressure. In addition, we found that citrate buffer with pH value around 3 dramatically increased the regeneration of protoplasts of A. cinnamomea, and provided a set of regeneration methodology for A. cinnamomea.

• 생명과학회지
• /
• 제13권2호
• /
• pp.143-149
• /
• 2003

This experiment was undertaken to investigate proper conditions for protoplast isolation and regeneration from the mycelia of Lyophyllum ulmnrium. Protoplast isolation and regeneration are influenced by a variety of factors such as enzyme, osmotic stabilizer, reaction time and age of mycelia. A combination of Novozyme 234 (10mg/ml) and cellulase Onozuka R-10 (10 mg/ml) with 0.6 M $MgSO_4$ was most effective for isolation of the protoplasts. The optimum reaction time of the mycelia with the lytic enzymes was 3.5~4 hours at $28^{\circ}C$ in shaking condition at 120 strokes per min. High yield of the protoplasts were obtained from its 4~5 days old mycelia on complete agar media. Its protoplasts were regenerated to normal hyphae. Regeneration media with 0.6 M sucrose were proper for regeneration of the protoplasts. Their regeneration frequency on complete agar media was 2.3~2.7%.

• 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.

• 한국균학회지
• /
• 제21권1호
• /
• pp.1-8
• /
• 1993

Phytophthora capsici에서 원형질체를 형성, 재생 시키는데 관여하는 요인에 대해 조사연구하였다. 삼투압조절제로서 0.35 M $CaCl_2$가 첨가된 Novozym 234를 6-9시간 처리하면 균사체에서 원형질체가 양호하게 나출되었다. 24시간 배양한 어린 균사체에서 가장 많이 원형질체를 나출시킬 수 있었으며, 또한 Novozym 234의 농도가 진할수록 효과적으로 원형질체가 나출되었다. 원형질체를 재생시키는데는 0.4 M mannitol과 0.1 M $CaCl_2$를 혼합한 것이 삼투압 조절제이었다. 원형질체의 재생률은 모든 영양소가 첨가된 Henninger 합성배지에서 가장 높았다. 아미노산이나 ${\beta}-sitosterol$은 원형질체의 재생에 영향을 미쳐 두 영양소가 빠지면 원형질체의 재생이 억제되었다. 특히 아미노산 중 L-aspartic acid와 L-glutamic acid는 원형질체의 재생을 촉진시켰다. 그러나, 미량원소는 원형질체의 재생에 영향을 주지 않았다.

• 한국미생물·생명공학회지
• /
• 제13권2호
• /
• pp.145-149
• /
• 1985

전분자원의 효율적 이용을 위한 방법의 일환으로 분리동정된 전분이용성 효모 H. anomala var. anomala FRI YO-32와 S. cerevisiae와의 세포융합가능성을 검토하기 위하여, 두 효모원형질체의 재생을 위한 최적조건들이 검토되었다. S. cerevisiae에 비하여 FRI YO-32균주의 원형질체가 삼투압안정성이 더 좋았으며 원형질체 재생에 영향을 주는 중요한 인자로서 agar와 삼투압안정제의 농도, 원형 질체 배양방법 등이 검토되었다. 또한 원형 질체 형성을 위한 효소처리 시간이 길어질수록 원형 질체 형성수율은 증가하나 재생효율은 감소하였다.

• Archives of Pharmacal Research
• /
• 제10권3호
• /
• pp.158-164
• /
• 1987

To obtain a new strain of Ganoderma lucidum by protoplast fusion technique, its protoplast formation and regeneration were studied. Several factors affecting the protoplast formation and regeneration were investigated to find their optimum conditions. The mycelium was grown for four days on the cellophane membrane placed on G. Incidum complete medium (GCM). When various commercial lytic enzymes were examined for protoplast isolation, the combination of Novozym 234 and $\beta$glucuronidase was found to be effective. An osmotic stabilizer, 0.6 M sucrose in 20 mM phosphate buffer pH 5.8, gave the highest yield of protoplasts. Three-hour incubation in shaking incubator was most suitable for releasing protoplasts. To increase the protoplast yield, pretreatment with 2-mercaptoethanol was carried out. The regeneration frequency in GCM containing 0.6M MgSO$_4$ 7$H_2O$ was shown to be 0.66%.

• Applied Microscopy
• /
• 제13권1호
• /
• pp.49-61
• /
• 1983

Protoplast releasing mechanisms from Trichoderma koningii, fine structures of the released protoplsts, and their regeneration mode were studied by scanning and transmission electron microscopy. Two types of protoplast releasing mechanisms were observed. In one mechanism, cytoplasm emerged through a cell wall pore developed by cell lytic enzymes and formed a spherical protoplast. In the other mechanism, as the cell wall became progressively thinner, the inner cytoplasm partially rounded to form nonspherical bodies which became spherical protoplasts after being released into the enzyme solution. But, these two types of protoplast releasing mechanisms did not seem to be. mutually exclusive but could occur on the same mycelium simultaneously. And it appeared that cytoplasm which did not become a protoplast by the first mechanism could from a protoplast by the second mechanism. The preparations contained two types of protoplasts, released from different sites of the mycelia. Those released from younger mycelia had dense cytoplasm and small vesicles. Those released from the older mycelia had less dense cytoplasm and larger vacuoles. In the case of regeneration, before producing normal mycelia, most of the protoplasts assumed aberrant tube and yeast-like-forms. Normal mycelia were produced at the end of the yeastlike-forms and sometimes in the middle of the aberrant tube.

• 한국미생물·생명공학회지
• /
• 제15권2호
• /
• pp.89-94
• /
• 1987

Streptomyces mitakaensis 균주의 원형질체 형성과 정상세포로의 재생에 관한 최적조건을 연구했다. S. mitakaensis 균주를 GBYN 배지(glycerol 20g, beef extract 5g, yeast extract 5g과 NaCl 5g, 증류수 1,000$m\ell$)에 glycine 0.5% 함유된 배지에서 대수증식 기말까지 배양한 뒤에 lysozyme(1mg/$m\ell$)을 35$^{\circ}C$에서 60분간 처리를 했을 때에 원형질체 형성은 최고치를 나타냈다. 정상세포로의 재생은 R2 평판배지에 원형질체를 접종한 후 10일이 됐을 때에 재생이 되는 것을 관찰했고, H2액체 배지에서는 3일 후에 재생되는 것을 관찰했다. 세포재생 비율은 0. 1% 정도였다.

• 한국미생물·생명공학회지
• /
• 제14권3호
• /
• pp.251-257
• /
• 1986

Lactobacillus casei 균주의 protoplast 형성과 정상세포로의 재생에 관한 최적조건이 연구되었다. Lactobacilus casei 균주들은 sucrose 1 mole이 함유된 20mM potassium phosphate완충액 (pH6.8)에서 mutanolysin을 10 $\mu\textrm{g}$/$m{\ell}$ 농도로 처리하였을 때 용이하게 protoplast가 형성되었다. Protoplast의 최대형성은 균주가 0. 5%의 glycine이 함유된 TCM 배지에서 생장이 대수기 중기에서 말기에 도달된 세포를 수확하여 사용했을 때에 이루어졌다. 세포 재생은 6 mM CaCl$_2$, 6mM MgCl$_2$, 0.8 M sucrose 그리고 horse serum 10%가 함유한 재생 배지에서 효율적으로 이루어 졌다. Protoplast의 세포벽 재생 빈도는 3$0^{\circ}C$에서 3-4 일간 배양후 2-5% 범위로 나타났다.