LaFauci G, Widom R L, Eisner R L, Jarvis E D, Rudner R
J Bacteriol. 1986 Jan;165(1):204-14. doi: 10.1128/jb.165.1.204-214.1986.
Integrable plasmids pGR102 and pWR103 containing ribosomal sequences from within the transcriptional units for 16S and 23S were used to transform Bacillus subtilis. To date, these plasmids integrated into 7 of 10 known rrn operons. Two such events occurred at unassigned operons, revealing a close linkage of the CAT gene of the plasmid to pha-1 situated between dal-1 and purB33 for rrnE and to thiA78 situated between glyB133 and re-12 for rrnD. All seven integration events that led to the loss of unique ribosomal BclI fragments can now be assigned to known rrn operons.
含有来自16S和23S转录单元内核糖体序列的可整合质粒pGR102和pWR103被用于转化枯草芽孢杆菌。到目前为止,这些质粒已整合到10个已知rrn操纵子中的7个。在未分配的操纵子中发生了两起这样的事件,揭示了质粒的CAT基因与rrnE的pha-1紧密连锁,pha-1位于dal-1和purB33之间;与rrnD的thiA78紧密连锁,thiA78位于glyB133和re-12之间。所有导致独特核糖体BclI片段丢失的七个整合事件现在都可以归因于已知的rrn操纵子。