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四个肌动蛋白结合蛋白编码基因agfA、fimA、sefA和sefD在肠炎沙门氏菌和/或鼠伤寒沙门氏菌XbaI - BlnI基因组限制性酶切图谱上的位置。

The location of four fimbrin-encoding genes, agfA, fimA, sefA and sefD, on the Salmonella enteritidis and/or S. typhimurium XbaI-BlnI genomic restriction maps.

作者信息

Collinson S K, Liu S L, Clouthier S C, Banser P A, Doran J L, Sanderson K E, Kay W W

机构信息

Department of Biochemistry and Microbiology, University of Victoria, British Columbia, Canada.

出版信息

Gene. 1996 Feb 22;169(1):75-80. doi: 10.1016/0378-1119(95)00763-6.

Abstract

Four fimbrin-encoding genes, fimA (type-1 or SEF21 fimbriae), agfA (thin aggregative or SEF17 fimbriae), sefA (SEF14 fimbriae and sefD (SEF18 fimbriae) from Salmonella enteritidis (Se) 27655-3b were located onto the XbaI-BlnI genomic restriction maps of Salmonella typhimurium (St) LT2 and Se strains SSU7998 and 27655-3b. The XbaI or BlnI genomic fragments carrying these genes were identified by hybridization with labeled oligodeoxyribonucleotides or fimbrin-encoding genes. The fimbrin-encoding genes were not encoded by the virulence plasmids, but were located on chromosomal DNA fragments. The position of each gene on a given XbaI fragment was determined by hybridization of a series of XbaI-digested genomic DNA samples from previously characterized Tn10 mutants of Se and St with its respective probe. The fimA gene mapped near 13 centisomes (Cs) between purE884::Tn10 at 12.6 Cs (11.8 min) and apeE2::Tn10 at 12.8 Cs (12.3 min) beside the first XbaI site at 13.0 Cs in St or between purE884::Tn10 at 12.6 Cs and the XbaI site at 13.6 Cs in Se. The agfA gene mapped near 26 Cs between putA::Tn10 and pyrC691::Tn10 in St, but near 40 Cs between pncX::Tn10 and the XbaI site at 43.3 Cs in Se. This difference in map position was due to the location of agfA near one end of the 815-kb chromosomal fragment inverted between Se and St. The sefA and sefD genes mapped precisely at 97.6 Cs in Se, but were absent from the genome of St LT2. To verify the mapping procedures used herein, tctC was also mapped in both Salmonella serovars. As expected, tctC mapped near 60 Cs in both St and Se, thereby confirming previous studies.

摘要

将肠炎沙门氏菌(Se)27655 - 3b的4个菌毛蛋白编码基因,即fimA(1型或SEF21菌毛)、agfA(细聚集性或SEF17菌毛)、sefA(SEF14菌毛)和sefD(SEF18菌毛)定位到鼠伤寒沙门氏菌(St)LT2以及Se菌株SSU7998和27655 - 3b的XbaI - BlnI基因组限制酶切图谱上。通过与标记的寡脱氧核糖核苷酸或菌毛蛋白编码基因杂交,鉴定出携带这些基因的XbaI或BlnI基因组片段。菌毛蛋白编码基因并非由毒力质粒编码,而是位于染色体DNA片段上。通过用来自先前鉴定的Se和St的Tn10突变体的一系列XbaI酶切基因组DNA样品与其各自的探针杂交,确定每个基因在给定XbaI片段上的位置。fimA基因在St中位于13.0 Cs处的第一个XbaI位点旁边,在12.6 Cs(11.8分钟)的purE884::Tn10和12.8 Cs(12.3分钟)的apeE2::Tn10之间,距离约13个厘摩(Cs);在Se中位于12.6 Cs的purE884::Tn10和13.6 Cs的XbaI位点之间。agfA基因在St中位于putA::Tn10和pyrC691::Tn10之间,距离约26 Cs;但在Se中位于pncX::Tn10和43.3 Cs的XbaI位点之间,距离约40 Cs。图谱位置的这种差异是由于agfA位于Se和St之间倒位的815 - kb染色体片段的一端附近。sefA和sefD基因在Se中精确地定位在97.6 Cs处,但在St LT2的基因组中不存在。为了验证本文使用的定位程序,还在两种沙门氏菌血清型中对tctC进行了定位。正如预期的那样,tctC在St和Se中均定位在60 Cs附近,从而证实了先前的研究。

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