Solovieva Irina M, Kreneva Rimma A, Errais Lopes Lubov, Perumov Daniel A
Molecular and Radiation Biophysics Division, St. Petersburg Nuclear Physics Institute of the Russian Academy of Sciences, Gatchina, Leningrad district 188350, Russia.
FEMS Microbiol Lett. 2005 Feb 1;243(1):51-8. doi: 10.1016/j.femsle.2004.11.038.
The riboflavin kinase encoding gene ribR is situated within a 12 genes locus ytmI-ytnM of the Bacillus subtilis chromosome. Here we demonstrate that ribR is transcribed as part of a 10 kb ytmI-ytnM operon. The riboflavin overproduction phenotype of B. subtilis ribC mutant strains, which is a result of the strongly reduced flavokinase activity of the riboflavin kinase/FAD synthetase RibC, was suppressed by ribR expression. Analysis of mutations with an upregulated ribR gene revealed 2 different groups of mutants. One class of mutants contained base substitutions in an 8 nucleotide sequence of the promoter region of the ytmI-ytnM operon. A second class of mutants had single point mutations within the yrzC gene or in the RBS of this gene. Dot-blot analysis of ytmI-ytnM transcription and the results of in trans complementation experiments for the yrzC mutants confirmed a role of the yrzC gene product as a negative regulator for the ytmI-ytnM operon.
编码核黄素激酶的基因ribR位于枯草芽孢杆菌染色体的一个包含12个基因的ytmI - ytnM基因座内。在此我们证明ribR作为一个10 kb的ytmI - ytnM操纵子的一部分被转录。枯草芽孢杆菌ribC突变株的核黄素过量生产表型是核黄素激酶/FAD合成酶RibC的黄素激酶活性大幅降低的结果,该表型被ribR的表达所抑制。对ribR基因上调的突变体分析揭示了2种不同类型的突变体。一类突变体在ytmI - ytnM操纵子启动子区域的一个8核苷酸序列中存在碱基替换。另一类突变体在yrzC基因内或该基因的核糖体结合位点(RBS)有单点突变。ytmI - ytnM转录的点杂交分析以及yrzC突变体的反式互补实验结果证实了yrzC基因产物作为ytmI - ytnM操纵子负调控因子的作用。