首页> 美国卫生研究院文献>Journal of Virology >Excision and duplication of su3+-transducing fragments carried by bacteriophage phi 80. I. Novel structure of phi 80sus2psu3+ DNA molecule.
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Excision and duplication of su3+-transducing fragments carried by bacteriophage phi 80. I. Novel structure of phi 80sus2psu3+ DNA molecule.

机译:噬菌体phi 80携带的su3 +转导片段的切除和重复。I. phi 80sus2psu3 + DNA分子的新结构。

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摘要

DNA molecules of phi 80sus2psu3+ and phi 80dsu3+ isolated by Andoh and Ozeki (1968) were studied by the electron microscope heteroduplex method. The phi 80sus2psu3+ and phi 80dsu3+ DNA lengths were found to be 108.7 and 103.3% of the phi 80 DNA, respectively. The phi 80sus2psu3+/phi 80 heteroduplex shows an insertion loop of 8.7% of the phi 80 DNA which migrates from 7.7 to 9.7%, as measured relative to the left (0%) and right (100%) termini of the mature phi 80 DNA molecule. The region of loop migration occupies the central region of the phi 80 head gene cluster. The presence of su3+-containing Escherichia coli DNA of 6.7% phi 80 unit flanked by two homologous regions of phage DNA of 2.0% of phi 80 unit gives rise to a movable insertion loop. In phi 80dsu3+, from which phi 80sus2psu3+ was derived, 50.5% of the phi 80 DNA at the left arm was replaced by E. coli DNA containing the su3+ gene, equivalent to about 53.8% phi 80 unit in length. The phi 80sus2psu3+/phi 80dsu3+ heteroduplex appears as a double-stranded molecule that bifurcates into two clearly visible single-stranded regions, rejoins, bifurcates, and rejoins again. The middle double-stranded stretches of 6.7% phi 80 unit correspond to the E. coli DNA inserted in phi 80sus2psu3+. Therefore the transducing fragment carried by phi 80sus2psu3+ originates from the inside region of the transducing fragment of defective phage phi 80dsu3+ by at least two illegitimate recombination events.
机译:用电子显微镜异源双链体方法研究了由安藤和大关(1968)分离的phi 80sus2psu3 +和phi 80dsu3 +的DNA分子。发现phi 80sus2psu3 +和phi 80dsu3 + DNA长度分别为phi 80 DNA的108.7%和103.3%。 phi 80sus2psu3 + / phi 80异源双链体显示了phi 80 DNA的8.7%的插入环,相对于成熟phi 80 DNA的左端(0%)和右端(100%)而言,它从7.7迁移到9.7%。分子。环迁移的区域占据了phi 80 head基因簇的中心区域。含su7 +的6.7%phi 80单位的大肠杆菌DNA与两个80%phi 80单位的噬菌体DNA的同源区域相接,形成了一个可移动的插入环。在派生phi 80sus2psu3 +的phi 80dsu3 +中,左臂的phi 80 DNA的50.5%被含有su3 +基因的大肠杆菌DNA所取代,相当于长度为约53.8%phi 80单位。 phi 80sus2psu3 + / phi 80dsu3 +异源双链体显示为双链分子,分叉成两个清晰可见的单链区域,重新连接,分叉,然后再次重新连接。中间6.7%的phi 80单位的双链延伸对应于插入phi 80sus2psu3 +中的大肠杆菌DNA。因此,通过至少两个非法重组事件,由phi 80sus2psu3 +携带的转导片段源自缺陷噬菌体phi 80dsu3 +的转导片段的内部区域。

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