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机构地区:[1]长春解放军农牧大学军事兽医研究所农学农机系,长春130062
出 处:《微生物学杂志》1999年第1期19-23,共5页Journal of Microbiology
基 金:吉林省科委资助
摘 要:研究了康氏木霉B-7和黑曲霉X-152株纤维素酶高产菌株的原生质体制备与再生。结果表明,采用纤维素酶、蜗牛酶、溶菌酶的混合酶液,可成功地制备2株真菌的原生质体。其中,B-7以这3种酶的配比6:5:2为最佳,X-15以8:4:2为最佳。原生质体形成的缓冲液系统均以0.2mol/L,pH6.0磷酸盐缓冲液为宜,渗透压稳定剂则分别以0.6mol/LNaCl和0.6mol/L蔗糖为宜。以菌龄18h(B-7)和16h(X-15)2株真菌的菌丝体,在37℃下酶解90min可获得最适量的原生质体,产量分别达9×106个/ml和1.9×107个/ml,且其再生率也较高,均达95%左右。The preparation and regeneration of protoplasts from two high - yield cellulase - produc-ing fungal strains, Trichoderma koningii B - 7 and Aspergillus nipe X - 15 were obtainedsuccessfully by using a mixed enzyme soution of cellulase, snail enzpe, and lysozyme. Theoptimum proportion of the enzymes were 6: 5: 2 (B - 7) and 8: 4: 2 (X -15) respectively.Phosphate buffer (0. 2mol/L at pH 6. 0) was suitable buffer for protopast formation. Silu-tion of 0. 6mol/L of NaCl for B - 7 and 0. 6mol/L of sucme for X - 15 were the suitable os-motic stabilizer respectively. The mycelia of 18h old for B - 7 and 16h old for X - 15 could beenzyme- digested in 90min at 37℃, and just to the right amount of protoplasts were ob-tained. The yields were up to 9X106/ml (B - 7), and 1. 9X107/ml (X - 15) respectively.And the regeneration rate of the protolasts was also high, it was around 95%.
分 类 号:TQ926.4[轻工技术与工程—发酵工程] Q949.327.1[生物学—植物学]
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