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Abstract:
12%的蔗糖浓度、0.5%甘氨酸、溶菌酶酶解1h,是金色链霉菌原生质体制备的较优条件.采用麸皮再生培养基替代R2YE再生培养基,原生质体再生率、生长及筛选效果得到明显改善.P-buffer介导的质粒转化效率高于T-buffer,33%的PEG1000是质粒转化金色链霉菌原生质的最适浓度.
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微生物学通报
ISSN: 0253-2654
CN: 11-1996/Q
Year: 2002
Issue: 5
Volume: 29
Page: 14-17
Cited Count:
SCOPUS Cited Count:
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 2
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