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克隆于质粒上的大肠杆菌核糖体蛋白及RNA聚合酶基因的表达。

Expression of Escherichia coli ribosomal protein and RNA polymerase genes cloned on plasmids.

作者信息

Fiil N P, Bendiak D, Collins J, Friesen J D

出版信息

Mol Gen Genet. 1979 May 23;173(1):39-50. doi: 10.1007/BF00267689.

Abstract

Fragments of lambda drifd 18 DNA with different end-points within the set of structural genes of ribosomal proteins L11 (RPLK), Li (rplA), L10 (rplJ) and L12 (rplL) as well as the beta (rpoB) ANd beta' (rpoC) subunits of RNA polymerase have been cloned on plasmids. These plasmids were transformed in host cells which were mutant for each of the genes, enabling expression of both wild-type (plasmid-borne) and mutant (chromosomal) genes to be differentiated. On the basis of these results we propose the following genetic structure for the region: rplK and rplA are in one operon; rplL, rpoB and rpoC are in a second. Our data suggest the possibility that rplJ is by itself in an operon situated between the other two.

摘要

已将λ噬菌体drifd 18 DNA片段克隆到质粒上,这些片段在核糖体蛋白L11(RPLK)、L1(rplA)、L10(rplJ)和L12(rplL)的结构基因以及RNA聚合酶的β(rpoB)和β'(rpoC)亚基组内具有不同的端点。这些质粒被转化到对每个基因均为突变型的宿主细胞中,从而能够区分野生型(质粒携带)和突变型(染色体)基因的表达。基于这些结果,我们提出该区域的以下遗传结构:rplK和rplA在一个操纵子中;rplL、rpoB和rpoC在第二个操纵子中。我们的数据表明,rplJ可能单独存在于位于其他两个操纵子之间的一个操纵子中。

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