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胞嘧啶脱氨酶MX盒作为酿酒酵母中的正/负选择标记

Cytosine deaminase MX cassettes as positive/negative selectable markers in Saccharomyces cerevisiae.

作者信息

Hartzog Phillip E, Nicholson Bradly P, McCusker John H

机构信息

Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Yeast. 2005 Jul 30;22(10):789-98. doi: 10.1002/yea.1245.

Abstract

We describe positive/negative selectable cytosine deaminase MX cassettes for use in Saccharomyces cerevisiae. The basis of positive selection for cytosine deaminase (Fcy1) activity is that (a) fcy1 strains are unable to grow on medium containing cytosine as a sole nitrogen source and (b) fcy1 ura3 strains are unable to grow on medium containing cytosine as the sole pyrimidine source. Conversely, as 5-fluorocytosine (5FC) is toxic to cytosine deaminase-producing cells, fcy1 strains are resistant to 5FC. FCY1MX and FCA1MX cassettes, containing open reading frames (ORFs) of S. cerevisiae FCY1 and Candida albicans FCA1, respectively, were constructed and used to disrupt targeted genes in S. cerevisiae fcy1 strains. In addition, new direct repeat cassettes, kanPR, FCA1PR, FCY1PR and CaURA3PR, were developed to allow efficient deletion of target genes in cells containing MX3 repeats. Finally, the FCY1- and FCA1MX3 or PR direct repeat cassettes can be readily recycled after 5FC counter-selection on both synthetic and rich media.

摘要

我们描述了用于酿酒酵母的正/负选择胞嘧啶脱氨酶MX盒。胞嘧啶脱氨酶(Fcy1)活性正选择的基础是:(a)fcy1菌株无法在以胞嘧啶作为唯一氮源的培养基上生长,以及(b)fcy1 ura3菌株无法在以胞嘧啶作为唯一嘧啶源的培养基上生长。相反,由于5-氟胞嘧啶(5FC)对产生胞嘧啶脱氨酶的细胞有毒,fcy1菌株对5FC具有抗性。分别构建了包含酿酒酵母FCY1和白色念珠菌FCA1开放阅读框(ORF)的FCY1MX和FCA1MX盒,并用于破坏酿酒酵母fcy1菌株中的目标基因。此外,还开发了新的直接重复盒,即kanPR、FCA1PR、FCY1PR和CaURA3PR,以允许在含有MX3重复序列的细胞中高效缺失目标基因。最后,在合成培养基和丰富培养基上进行5FC反选择后,FCY1-和FCA1MX3或PR直接重复盒可以很容易地回收利用。

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