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作 者:佘秋生[1] 杨海波[1] 杨冠军[1] 薛银磊[1] 祝小龙[1] 单林娜[1]
机构地区:[1]河南城建学院生物工程系,河南平顶山467036
出 处:《中国酿造》2012年第6期134-137,共4页China Brewing
基 金:河南城建学院科研基金项目(2010JYB013)
摘 要:以黑曲霉(Aspergilus niger)CICC41254为出发菌株,进行紫外线诱变。初筛使用透明圈法,从果胶平板上的突变菌株中,挑取了26株透明圈与菌落直径比值显著大于出发菌株的突变株。将这些突变株进行三角瓶固体发酵复筛,最后筛选出1株高产果胶酶的突变株CICC41254-D8。突变株CICC41254-D8经斜面传代培养了5代,产酶遗传特性稳定,其果胶酶活力最高可达1156.8U/g干基,比出发菌株酶活力(750.0U/g)提高了54.24%。Aspergilus niger CICC41254 was treated by ultraviolet radiation for the development of high pectinase-producing strain. Transparent circle method was used for preliminary screening, by which 26 mutant strains were selected with higher ratio of transparent circle diameter to colony diame-ter on pectin plate media. These mutant strains were re-screened by solid state fermentation in flasks, and one strain named CICC41254-D8 was se-lected with high pectinase-producing ability. CICC41254-D8 was incubated on slant through 5 generations. It was showed that the genetic expression of pectinase was stable. The pectinase activity could reach 1156.8U/gdry bionass which was 54.24% higher than that of the original strain (750.0U/g).
分 类 号:TS201.3[轻工技术与工程—食品科学]
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