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利用转座子插入zdc - 235::Tn10(最小32)从大肠杆菌末端区域克隆和删除DNA。

The use of transposon insertion zdc-235::Tn10 (min 32) to clone and delete DNA from the terminus region of Escherichia coli.

作者信息

Henson J M, Kuempel P L

出版信息

Mol Gen Genet. 1983;189(3):506-12. doi: 10.1007/BF00325918.

Abstract

Transposon zdc-235::Tn10 is inserted at min 32 on the genetic map of Escherichia coli, and we have used this transposon to clone 14 kb of DNA that flanks this insertion. The site of insertion of the transposon, and the restriction map of the cloned DNA, correspond well with the predictions of the Bouché restriction map for the terminus region (Bouché 1982). The zdc-235::Tn10 insertion, along with the zdd-230::Tn9 insertion, was used to obtain deletions of the region that has been cloned. Strains lacking a minimum of 14 kb, and more likely a minimum of 40 kb of DNA, showed no alteration of growth or cell morphology.

摘要

转座子zdc - 235::Tn10插入在大肠杆菌基因图谱的32分钟处,我们利用这个转座子克隆了位于该插入位点两侧的14kb DNA。转座子的插入位点以及克隆DNA的限制酶切图谱,与布歇(Bouché)对末端区域的限制酶切图谱预测结果非常吻合(布歇,1982年)。zdc - 235::Tn10插入以及zdd - 230::Tn9插入被用于获得已克隆区域的缺失突变体。缺失至少14kb,更可能是至少40kb DNA的菌株,其生长或细胞形态没有改变。

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