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利用Tn917在A群链球菌中产生插入突变。

Use of Tn917 to generate insertion mutations in the group A streptococcus.

作者信息

Eichenbaum Z, Scott J R

机构信息

Department of Microbiology and Immunology, Emory University, Atlanta, GA 30322, USA.

出版信息

Gene. 1997 Feb 28;186(2):213-7. doi: 10.1016/s0378-1119(96)00705-6.

Abstract

The Enterococcus faecalis transposon Tn917 is functional in a broad range of bacteria, including both Gram-positive and Gram-negative species. We cloned Tn917-LTV3, a derivative carrying a promoterless lacZ (beta-galactosidase gene), into the thermosensitive shuttle replicon pG+host4 and assayed for chromosomal insertions in group A streptococcus (GAS). Tn917 transposed into the GAS chromosome at a frequency of (2.8 +/- 3.2) x 10(-5) per colony forming unit (cfu). Transposition products were predominantly simple insertions and no target site preference was detectable. Some transcriptional fusions were identified in which the promoterless lacZ of the transposon appeared to be expressed from an external promoter.

摘要

粪肠球菌转座子Tn917在广泛的细菌中具有功能,包括革兰氏阳性菌和革兰氏阴性菌。我们将携带无启动子lacZ(β-半乳糖苷酶基因)的衍生物Tn917-LTV3克隆到温度敏感穿梭复制子pG+host4中,并检测其在A组链球菌(GAS)中的染色体插入情况。Tn917以每集落形成单位(cfu)(2.8 +/- 3.2) x 10(-5) 的频率转座到GAS染色体中。转座产物主要是简单插入,未检测到靶位点偏好。鉴定出一些转录融合体,其中转座子的无启动子lacZ似乎由外部启动子表达。

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