Analysis of cepA and other Bacteroides fragilis genes reveals a unique promoter structure

被引:111
作者
Bayley, DP [1 ]
Rocha, ER [1 ]
Smith, CJ [1 ]
机构
[1] E Carolina Univ, Sch Med, Dept Microbiol & Immunol, Greenville, NC 27858 USA
关键词
transcription; promoter; cepA; Bacteroides fragilis;
D O I
10.1016/S0378-1097(00)00472-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
There is little known about the sequences that mediate the initiation of transcription in Bacteroides fragilis, thus transcriptional start sites for 13 new genes were determined and a total of 23 promoter regions upstream of the start sites were aligned and similarities were noted. A region at about -7 contained a consensus sequence of TAnnTTTG and upstream in the region centered at about -33, another TTTG motif was found in the majority of promoters examined. Canonical, Escherichia coli, -10 and -35 consensus sequences were not readily apparent. Mutations within the -7 motif indicated the TTTG residues were essential since changes in this sequence reduced the promoter activity to that of a no promoter control in a chloramphenicol acetyl transferase transcriptional fusion model system. Additional fusion studies indicated that the -33 region was also necessary for Full activity. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 154
页数:6
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