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Plasmids carrying oriC can integrate at or near the chromosome origin of Escherichia coli in the absence of a functional recA product.

作者信息

Masters M, Andresdottir V, Wolf-Watz H

出版信息

Cold Spring Harb Symp Quant Biol. 1979;43 Pt 2:1069-72. doi: 10.1101/sqb.1979.043.01.118.

DOI:10.1101/sqb.1979.043.01.118
PMID:385219
Abstract
摘要

相似文献

1
Plasmids carrying oriC can integrate at or near the chromosome origin of Escherichia coli in the absence of a functional recA product.
Cold Spring Harb Symp Quant Biol. 1979;43 Pt 2:1069-72. doi: 10.1101/sqb.1979.043.01.118.
2
[Dependence of recA gene for the replication of chromosome of Escherichia coli initiated by the integrated mini-F plasmid carrying IS1 sequence].[携带IS1序列的整合型mini-F质粒引发的大肠杆菌染色体复制对recA基因的依赖性]
Yi Chuan Xue Bao. 1990;17(6):476-83.
3
Conjugal transmission of plasmids.质粒的配偶传递
Annu Rev Genet. 1979;13:99-125. doi: 10.1146/annurev.ge.13.120179.000531.
4
Maintenance and incompatibility of plasmids carrying the replication origin of the Escherichia coli chromosome: evidence for a control region of replication between oriC and asnA.携带大肠杆菌染色体复制起点的质粒的维持与不相容性：oriC和asnA之间存在复制控制区域的证据
Nucleic Acids Res. 1983 Aug 25;11(16):5775-91. doi: 10.1093/nar/11.16.5775.
5
Studies on the role of dam methylation at the Escherichia coli chromosome replication origin (oriC).关于大肠杆菌染色体复制起点（oriC）处DNA甲基化作用的研究。
Adv Exp Med Biol. 1984;179:543-9. doi: 10.1007/978-1-4684-8730-5_57.
6
Multiple origin usage for DNA replication in sdrA(rnh) mutants of Escherichia coli K-12. Initiation in the absence of oriC.大肠杆菌K-12的sdrA(rnh)突变体中DNA复制的多起点使用。在无oriC情况下的起始。
J Mol Biol. 1984 Sep 15;178(2):227-36. doi: 10.1016/0022-2836(84)90141-4.
7
The 245 base-pair oriC sequence of the E. coli chromosome directs bidirectional replication at an adjacent region.大肠杆菌染色体的245个碱基对的oriC序列在相邻区域指导双向复制。
Nucleic Acids Res. 1983 May 11;11(9):2617-26. doi: 10.1093/nar/11.9.2617.
8
[Participation of plasmid F in the replication of the chromosome of an Hfr strain of Escherichia coli K-12].[质粒F参与大肠杆菌K - 12 Hfr菌株染色体的复制]
Genetika. 1983 Mar;19(3):416-24.
9
[Replication characteristics of plasmids and their dependence of recA gene for the initiation of Escherichia coli chromosome replication in the integrated state].[整合状态下质粒的复制特性及其recA基因对大肠杆菌染色体复制起始的依赖性]
Yi Chuan Xue Bao. 1990;17(1):53-62.
10
Site-specific integration of an F' lac pro factor in the region of the replication origin (oriC) of E. coli.F' lac pro 因子在大肠杆菌复制起点（oriC）区域的位点特异性整合。
Mol Gen Genet. 1980;179(2):437-46. doi: 10.1007/BF00425474.

引用本文的文献

1
The segregation of Escherichia coli minichromosomes constructed in vivo by recombineering.体内重组构建的大肠杆菌小型染色体的分离。
Plasmid. 2012 Mar;67(2):148-54. doi: 10.1016/j.plasmid.2012.01.002. Epub 2012 Jan 10.
2
oriC region and replication termination site, dif, of the Xanthomonas campestris pv. campestris 17 chromosome.野油菜黄单胞菌野油菜致病变种17号染色体的oriC区域和复制终止位点dif。
Appl Environ Microbiol. 2002 Jun;68(6):2924-33. doi: 10.1128/AEM.68.6.2924-2933.2002.
3
Suppressor mutations (rin) that specifically suppress the recA+ dependence of stable DNA replication in Escherichia coliK-12.
抑制突变（rin），其可特异性抑制大肠杆菌K-12中稳定DNA复制对recA+的依赖性。
Mol Gen Genet. 1982;187(2):225-30. doi: 10.1007/BF00331121.
4
The genes for the eight subunits of the membrane bound ATP synthase of Escherichia coli.大肠杆菌膜结合ATP合酶八个亚基的基因。
Mol Gen Genet. 1981;183(3):463-72. doi: 10.1007/BF00268766.
5
Pseudovirulent mutants of lambda b221poriCasnA resulting from mutations in or near oriC, the E. coli origin of DNA replication.由大肠杆菌DNA复制起点oriC及其附近的突变产生的λb221poriCasnA假毒力突变体。
Mol Gen Genet. 1980;178(2):391-6. doi: 10.1007/BF00270489.
6
Isolation and characterization of lambda b221poriCasnA, a plaque-forming specialized transducing phage carrying the origin of replication of the Escherichia coli chromosome.λb221poriCasnA的分离与特性鉴定，λb221poriCasnA是一种携带大肠杆菌染色体复制起点的噬菌斑形成特异性转导噬菌体。
Mol Gen Genet. 1980;178(2):381-9. doi: 10.1007/BF00270488.
7
Affinity of two different regions of the chromosome to the outer membrane of Escherichia coli.染色体两个不同区域与大肠杆菌外膜的亲和力。
J Bacteriol. 1984 Mar;157(3):968-70. doi: 10.1128/jb.157.3.968-970.1984.
8
Expression of a neomycin phosphotransferase gene from Streptomyces fradiae in Escherichia coli after interplasmidic recombination.经质体间重组后，弗氏链霉菌新霉素磷酸转移酶基因在大肠杆菌中的表达。
Mol Gen Genet. 1983;189(1):27-33. doi: 10.1007/BF00326051.
9
Copy number mutations (Cop-) of the plasmid containing the replication origin (oriC) of the Escherichia coli chromosome: lethal effect of the cop region cloned onto a high-copy-number vector on host cells.
J Bacteriol. 1983 Jan;153(1):550-4. doi: 10.1128/jb.153.1.550-554.1983.
10
Use of lambda unc transducing bacteriophages in genetic and biochemical characterization of H+-ATPase mutants of Escherichia coli.λ unc 转导噬菌体在大肠杆菌 H⁺-ATP 酶突变体的遗传和生化特性研究中的应用
J Bacteriol. 1983 Dec;156(3):1078-92. doi: 10.1128/jb.156.3.1078-1092.1983.