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投稿时间:2018-05-23
投稿时间:2018-05-23
中文摘要: 为完善高效的黑曲霉工程菌10142基因敲除体系,提高其基因敲除效率,构建含有致死基因单纯疱疹病毒胸苷激酶(herpes simplex virus thymidine kinase,HSVtk)的基因敲除质粒,通过农杆菌介导的黑曲霉转化(Agrobacterium tumefaciens-mediated transformation,ATMT)法,使致死基因随机插入黑曲霉基因组,其阳性转化子在添加10 μmol/L的5-氟脱氧尿苷的培养基上无法生长,从而得到致死基因随机插入转化子的“反向筛选”方法。利用该方法对黑曲霉海藻糖-6-磷酸合成酶进行基因敲除,结果表明阳性转子占总转化子的比例为63%。成功构建高效黑曲霉基因敲除体系。
中文关键词: 黑曲霉 基因敲除 致死基因 5-氟脱氧尿苷 海藻糖-6-磷酸合成酶
Abstract:Abstract:An efficient method of gene knockout system was developed in Aspergillus niger 10142,an hyperproducer of citric acid fermentation.It constructed a binary vector containing lethal genes that a herpes simplex virus thymidine kinase(HSVtk)gene in T-DNA.By using Agrobacterium tumefaciens-mediated transformation(ATMT),the ectopic transformants did not grow on the medium addition of 10 μmol/L 5-fluoro-2'-deoxyuridine.This method increased the proportion of positive transformants to select gene knockout transformants.Gene knockout experiments on trehalose-6-phosphate synthase(tpsA)in Aspergillus niger were performed using double-tagged vector containing lethal gene and hygromycin.The results showed that the frequency which refered to positive number account for total transformants was 63%.The successful construction of Aspergillus niger gene knockout system has provided an efficient technology platform for gene knockout experiments and researchment on the gene mechanisms of Aspergillus niger.
keywords: Key words:Aspergillus niger gene knockout lethal gene 5-fluoro-2'-deoxyuridine trehalose-6-phosphate synthase
文章编号:201822021 中图分类号: 文献标志码:
基金项目:
作者 | 单位 |
刘玲,张鸿飞,张岚,秦郦,王德培 | (1.工业发酵微生物教育部重点实验室,天津300457;2.省部共建食品营养与安全国家重点实验室,天津300457;3.天津科技大学生物工程学院,天津300457) |
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