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大肠杆菌复制起点在单链DNA噬菌体中的克隆与表达。

Cloning and expression of the Escherichia coli replication origin in a single-stranded DNA phage.

作者信息

Kaguni J, LaVerne L S, Ray D S

出版信息

Proc Natl Acad Sci U S A. 1979 Dec;76(12):6250-4. doi: 10.1073/pnas.76.12.6250.

Abstract

The Escherichia coli DNA replication origin (oriC) and the adjacent asparagine synthetase gene (asnA) have been inserted into the duplex replicative form DNA of the single-stranded phage vector M13Goril. By in vitro recombination, the entire oriC asnA-containing plasmid pJS5 was inserted into M13Gori1 in both possible orientations. Both phage types transduce the asnA gene and confer upon the M13 vector the ability to replicate as a plasmid in the E. coli mutant rep3. In rep+ hosts, these phages undergo single-stranded DNA synthesis and viral morphogenesis.

摘要

大肠杆菌DNA复制起点(oriC)及相邻的天冬酰胺合成酶基因(asnA)已被插入单链噬菌体载体M13Goril的双链复制型DNA中。通过体外重组,整个含oriC asnA的质粒pJS5以两种可能的方向插入M13Gori1中。两种噬菌体类型都能转导asnA基因,并赋予M13载体在大肠杆菌突变体rep3中作为质粒进行复制的能力。在rep+宿主中,这些噬菌体进行单链DNA合成和病毒形态发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc53/411841/51217db08202/pnas00012-0235-a.jpg

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