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SPO1基因组的克隆与定位

Cloning and mapping of the SPO1 genome.

作者信息

Curran J F, Stewart C R

出版信息

Virology. 1985 Apr 15;142(1):78-97. doi: 10.1016/0042-6822(85)90424-6.

Abstract

Many of the XbaI, EcoRI, KpnI, and BglII fragments of bacteriophage SPO1, accounting for about 65% of the genomic sequences, were cloned in Bacillus subtilis. Four of the EcoRI fragments were specifically refractory to cloning in both Escherichia coli and B. subtilis, probably because of expression of deleterious genes carried on the SPO1 fragments. To permit complete identification of the regions cloned, the SPO1 restriction map has been extended to include the XbaI fragments and the previously unmapped KpnI fragments. Markers for 26 of the 39 known genes have been located on specific cloned fragments, permitting more precise determination of the positions of most of the genes. One cloned SPO1 fragment was inhibitory to SPO1 development.

摘要

噬菌体SPO1约65%的基因组序列中的许多XbaI、EcoRI、KpnI和BglII片段被克隆到枯草芽孢杆菌中。四个EcoRI片段在大肠杆菌和枯草芽孢杆菌中都特别难以克隆,这可能是因为SPO1片段上携带的有害基因的表达。为了能够完全鉴定所克隆的区域,SPO1限制酶切图谱已扩展到包括XbaI片段和先前未定位的KpnI片段。39个已知基因中的26个基因的标记已定位在特定的克隆片段上,从而能够更精确地确定大多数基因的位置。一个克隆的SPO1片段对SPO1的发育具有抑制作用。

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