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转座子Tn5的ble基因编码的博来霉素抗性作为酿酒酵母中的显性选择标记。

Phleomycin resistance encoded by the ble gene from transposon Tn 5 as a dominant selectable marker in Saccharomyces cerevisiae.

作者信息

Gatignol A, Baron M, Tiraby G

出版信息

Mol Gen Genet. 1987 May;207(2-3):342-8. doi: 10.1007/BF00331599.

Abstract

Phleomycin, a water-soluble antibiotic of the bleomycin family is as effective against Saccharomyces cerevisiae cells as against Escherichia coli cells. The ble gene of transposon Tn5, which confers resistance to phleomycin, was inserted in place of the iso-1-cytochrome C (CYC1) gene on an autonomously replicative multicopy E. coli-yeast shuttle plasmid. Higher resistance levels are obtained in S. cerevisiae when the region immediately upstream from the initiation codon conforms to the nucleotide sequence stringencies observed in almost every yeast gene. The expected regulation pattern of the whole CYC1 promoter confers different phleomycin resistance levels to the cell under varying physiological conditions. Partial deletions in the CYC1 promoter lead to changes in the resistance level of cells which are mostly accounted for by the removal of known positive and negative regulatory elements. Some of the vector constructions allow direct selection of phleomycin-resistant transformants on rich media.

摘要

博来霉素是博来霉素家族的一种水溶性抗生素,对酿酒酵母细胞和大肠杆菌细胞的作用效果相同。赋予博来霉素抗性的转座子Tn5的ble基因,被插入到自主复制的多拷贝大肠杆菌-酵母穿梭质粒上的异-1-细胞色素C(CYC1)基因的位置。当起始密码子上游紧邻区域符合几乎每个酵母基因中观察到的核苷酸序列严格性时,酿酒酵母中可获得更高的抗性水平。整个CYC1启动子的预期调控模式在不同生理条件下赋予细胞不同的博来霉素抗性水平。CYC1启动子中的部分缺失导致细胞抗性水平的变化,这主要是由于已知的正负调控元件的去除。一些载体构建允许在丰富培养基上直接筛选博来霉素抗性转化体。

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