江西农业大学学报
江西農業大學學報
강서농업대학학보
ACTA AGRICULTURAE UNIVERSITATIS JIANGXIENSIS
2015年
1期
84-89
,共6页
李霖%刘冰%陈秀润%崔朝宇%蒋军喜%胡琼波
李霖%劉冰%陳秀潤%崔朝宇%蔣軍喜%鬍瓊波
리림%류빙%진수윤%최조우%장군희%호경파
玫烟色棒束孢%原生质体%制备%转化
玫煙色棒束孢%原生質體%製備%轉化
매연색봉속포%원생질체%제비%전화
Isaria Fumosorosea%protoplast%preparation%transformation
为了提高虫生真菌玫烟色棒束孢IfB01原生质体的产量和转化效率,进而为该菌株的基因工程和细胞工程改良奠定基础,本文研究了不同细胞壁降解酶配比、渗透压稳定剂、酶解温度、时间、pH值和转速等对玫烟色棒束孢IfB01原生质体制备以及不同聚乙二醇4000( PEG4000)浓度对原生质体转化的影响。结果显示,培养30 h的菌丝用1%蜗牛酶+2%纤维素酶配比、以0.7 mol/L 的 NaCl 溶液(pH6.0)为渗透压稳定剂,30℃、100 r/min酶解8 h,获得的原生质体产量最高,达6.72×106个/mL;此原生质体在40%的PEG4000作用下可获得最高的转化效率,达7.05%。研究表明酶液、酶解温度、时间、pH值、渗透压、稳定剂、转速和PEG4000的浓度等因素对原生质体的制备和转化有较大影响。
為瞭提高蟲生真菌玫煙色棒束孢IfB01原生質體的產量和轉化效率,進而為該菌株的基因工程和細胞工程改良奠定基礎,本文研究瞭不同細胞壁降解酶配比、滲透壓穩定劑、酶解溫度、時間、pH值和轉速等對玫煙色棒束孢IfB01原生質體製備以及不同聚乙二醇4000( PEG4000)濃度對原生質體轉化的影響。結果顯示,培養30 h的菌絲用1%蝸牛酶+2%纖維素酶配比、以0.7 mol/L 的 NaCl 溶液(pH6.0)為滲透壓穩定劑,30℃、100 r/min酶解8 h,穫得的原生質體產量最高,達6.72×106箇/mL;此原生質體在40%的PEG4000作用下可穫得最高的轉化效率,達7.05%。研究錶明酶液、酶解溫度、時間、pH值、滲透壓、穩定劑、轉速和PEG4000的濃度等因素對原生質體的製備和轉化有較大影響。
위료제고충생진균매연색봉속포IfB01원생질체적산량화전화효솔,진이위해균주적기인공정화세포공정개량전정기출,본문연구료불동세포벽강해매배비、삼투압은정제、매해온도、시간、pH치화전속등대매연색봉속포IfB01원생질체제비이급불동취을이순4000( PEG4000)농도대원생질체전화적영향。결과현시,배양30 h적균사용1%와우매+2%섬유소매배비、이0.7 mol/L 적 NaCl 용액(pH6.0)위삼투압은정제,30℃、100 r/min매해8 h,획득적원생질체산량최고,체6.72×106개/mL;차원생질체재40%적PEG4000작용하가획득최고적전화효솔,체7.05%。연구표명매액、매해온도、시간、pH치、삼투압、은정제、전속화PEG4000적농도등인소대원생질체적제비화전화유교대영향。
In order to increase the yield and transformation efficiency of protoplast from Isaria fumosorosea strain IfB01,an entomopathogenic fungus,and then to lay a foundation for the strain improvement by genetic and cell engineering,the effects of selected parameters( concentration ratio of cell wall-degrading enzyme,en?zyme digestion time,temperature,pH value,rotating speed and concentration of osmotic stabilizer) on proto?plast preparation of I.fumosorosea strain IfB01,and the effects of different concentrations of PEG4000 on trans?formation efficiency of the fungus were examined.The highest protoplast yield of 6.72×106 per milliliter was ob?tained from 30 h-old mycelia after treatment with 1% snailase-2% cellulose,osmotic stabilizer of 0.7 mol/L NaCl(pH6.0),8 h of enzymolysis under 30℃,100 r/min.The highest transformation efficiency of 7.05% was obtained under the treatment of 40% PEG4000.It showed that enzyme solution,hydrolysis temperature,time, pH,osmotic pressure,stabilizer,speed and concentration of PEG4000 have great influence on protoplast prepa?ration and transformation.