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 $234+{eta}-D-glucanase;+{eta}-glucuronidase;mixture$에서 원형질체수(原形質體數)는 $10.55{ imes}10^6;ml^{-1}$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 $2.2{ imes}10^7;ml^{-1}$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.
The optimal conditions for high yields of mycelial protoplasts from P. cornucopiae were established. The concentraion of enzyme system containing Novozym 234, ${eta}-D-glucanase$ and ${eta}-glucuronidase$ was $5mg;ml^{-1}$ each. The osmotic stabilizer most effective for protoplast isolation was O.6 M sucrose. The optimal reaction time of mycelium with the lytic mixture was 90 min in a shaking condition at 120 strokes $min^{-1}$. When the myelium of P. cornucopiae was cultured for 4 days on mushroom complete medium at $28^{circ}C$, the formation of protoplast was effective. When the pH of the digestion mixture with O.6 M sucrose as stabilizer varied between pH 4.0 and 7.0, the production of protoplasts was effective in phosphate buffer (pH 6.2) and Na-maleate buffer (pH 5.0). Generally, phosphate buffer was more effective for protoplast isolation than Na-maleate buffer, but 0.6 M sucrose osmotic stabilizer without adjusting pH was most effective. Using these conditions, protoplasts from P. cornucopiae were obtained at a ratio $1{ imes}10^7;ml^{-1}$.
