首页> 外文期刊>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:由噬菌体PHI 80携带的SU3 + -Transduding片段的切除和重复。I. PHI 80SUS2PSU3 + DNA分子的新型结构。

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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:通过电子显微镜异透掺杂方法研究了由ANDOH和OZEKI(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异掺杂显示了8.7%的PHI 80DNA的插入回路,其迁移为7.7%至9.7%,如成熟PHI 80 DNA的左(0%)和右(100%)末端测量分子。环迁移区域占据PHI 80头基因簇的中心区域。由2.0%的PHI 80单元的两种噬菌体DNA的两个同源性区域侧翼的SU3 +型大肠杆菌DNA的存在导致可移动插入环。在PHI 80DSU3 +中,从中得出PHI 80SUS2PSU3 +,左臂的50.5%的PHI 80 DNA被含有SU3 +基因的大肠杆菌DNA取代,其长度为约53.8%PHI 80单位。 PHI 80SUS2PSU3 + / PHI 80DSU3 +异络表现为双链分子,其分为两个清晰可见的单链区域,再加速,分叉和再次重新冻结。中间双链拉伸的6.7%phi 80单元对应于插入的大肠杆菌DNA,插入PHI 80SUS2PSU3 +。因此,PHI 80SUS2PSU3 +携带的转晶片段由至少两种非法重组事件源自缺陷噬菌体PHI 80DSU3 +的转换片段的内部区域。

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