Salerno A J, Lampen J O
Waksman Institute of Microbiology, Rutgers, State University of New Jersey, Piscataway 08855-0759.
FEBS Lett. 1988 Jan 18;227(1):61-5. doi: 10.1016/0014-5793(88)81414-5.
Induction of beta-lactamase (blaP) in Bacillus licheniformis involves the regulatory genes blaI (repressor), blaR1 (coinducer) and R2 (function unknown). Transcription of the bla genes during induction was followed by Northern hybridization. In the first 30 min 2.3-kb transcripts encoding blaI and blaR1 were present. Subsequently, blaP mRNA and short transcripts encoding only blaI accumulated and reached a peak at 1 h. All bla transcripts turn over rapidly. Active repressor is not required for the burst of blaI-blaR1 mRNA. The production of blaI-blaR1 mRNA, and thus of BlaR1, is probably controlled both at initiation of transcription and at a later step in its synthesis and degradation.
地衣芽孢杆菌中β-内酰胺酶(blaP)的诱导涉及调控基因blaI(阻遏物)、blaR1(共诱导物)和R2(功能未知)。诱导过程中bla基因的转录通过Northern杂交进行跟踪。在最初的30分钟内,存在编码blaI和blaR1的2.3 kb转录本。随后,blaP mRNA和仅编码blaI的短转录本积累,并在1小时达到峰值。所有bla转录本周转迅速。blaI-blaR1 mRNA的爆发不需要活性阻遏物。blaI-blaR1 mRNA的产生,进而BlaR1的产生,可能在转录起始以及其合成和降解的后续步骤中都受到控制。