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用于插入诱变、基因融合和基因构建的uidA抗生素抗性盒。

'uidA-antibiotic-resistance cassettes for insertion mutagenesis, gene fusions and genetic constructions.

作者信息

Bardonnet N, Blanco C

机构信息

Laboratoire de Microbiologie, I.N.S.A., Villeurbanne, France.

出版信息

FEMS Microbiol Lett. 1992 Jun 15;72(3):243-7. doi: 10.1016/0378-1097(92)90469-5.

Abstract

We have constructed a series of promoterprobe cassettes that provides powerful tools for insertion mutagenesis, transcription fusions and genetic constructions. These cassettes contain the Tn9 chloramphenicol (CmR) and the Tn903 kanamycin (KmR) resistance genes which are expressed in a large variety of microorganisms; these antibiotic-resistance markers were associated with the uidA promoterless gene. This beta-glucuronidase-encoding gene of Escherichia coli K-12 has been successfully used as reporter gene for various organisms including prokaryotes and eukaryotes. The resulting 'uidA-KmR and 'uidA-CmR cassettes (truncated at the ') can be excized with most of the commonly used restriction enzymes. Furthermore, they are borne by ApR or CmR plasmids which facilitate their utilization. These promoter-probe cassettes allow transcriptional signal localization and regulation studies.

摘要

我们构建了一系列启动子探针盒,这些启动子探针盒为插入诱变、转录融合和基因构建提供了强大的工具。这些盒式结构包含Tn9氯霉素(CmR)和Tn903卡那霉素(KmR)抗性基因,它们在多种微生物中表达;这些抗生素抗性标记与无启动子的uidA基因相关联。大肠杆菌K-12的这个编码β-葡萄糖醛酸酶的基因已成功用作包括原核生物和真核生物在内的各种生物体的报告基因。所得的“uidA-KmR”和“uidA-CmR”盒式结构(在“处截断)可用大多数常用的限制性内切酶切除。此外,它们由ApR或CmR质粒携带,这便于它们的使用。这些启动子探针盒可用于转录信号定位和调控研究。

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