Martín M, Magni C, López P, de Mendoza D
Instituto de Biología Molecular y Celular de Rosario and Departamento de Microbiología, Universidad Nacional de Rosario, Argentina.
J Bacteriol. 2000 Jul;182(14):3904-12. doi: 10.1128/JB.182.14.3904-3912.2000.
In this study we describe the expression pattern of the Leuconostoc paramesenteroides citMCDEFGRP operon in response to the addition of citrate to the growth medium. An 8.8-kb polycistronic transcript, which includes the citMCDEFGRP genes, was identified; its synthesis was dramatically induced upon addition of citrate to the growth medium. We also found that expression of the cit operon is subjected to posttranscriptional regulation, since processing sites included in four complex secondary structures (I, II, III, and IV) were identified by Northern blot analysis and mapped by primer extension. Upstream of the citMCDEFGRP operon a divergent open reading frame, whose expression was also increased by citrate, was identified by DNA sequencing and designated citI. The start and end sites of transcription of the cit operon and citI gene were mapped. The start sites are separated by a stretch of 188 bp with a very high A+T content of 77% and are preceded by transcriptional promoters. The end sites of the transcripts are located next to the 3' end of two secondary structures characteristic of rho-independent transcriptional terminators. The effect of the citI gene on expression of the cit operon was studied in Escherichia coli. The presence of the citI gene in cis and in trans resulted in increased activity of the cit promoter. These data provide the first evidence that citrate fermentation in Leuconostoc is regulated at the transcriptional level by a transcriptional activator rather than by a repressor.
在本研究中,我们描述了副干酪乳杆菌citMCDEFGRP操纵子在向生长培养基中添加柠檬酸盐时的表达模式。鉴定出了一个包含citMCDEFGRP基因的8.8 kb多顺反子转录本;在向生长培养基中添加柠檬酸盐后,其合成被显著诱导。我们还发现cit操纵子的表达受到转录后调控,因为通过Northern印迹分析鉴定出了四个复杂二级结构(I、II、III和IV)中包含的加工位点,并通过引物延伸进行了定位。通过DNA测序在citMCDEFGRP操纵子上游鉴定出一个 divergent 开放阅读框,其表达也因柠檬酸盐而增加,并将其命名为citI。绘制了cit操纵子和citI基因转录的起始和终止位点。起始位点被一段188 bp的序列隔开,该序列的A+T含量非常高,为77%,并且前面有转录启动子。转录本的终止位点位于两个不依赖ρ的转录终止子特征性二级结构的3'端附近。在大肠杆菌中研究了citI基因对cit操纵子表达的影响。citI基因的顺式和反式存在导致cit启动子活性增加。这些数据提供了第一个证据,即副干酪乳杆菌中的柠檬酸盐发酵在转录水平上由转录激活因子而非阻遏因子调控。