Vecerek B, Venema G
Laboratory of Enzyme Technology, Institute of Microbiology CAS, Prague, Czech Republic.
J Bacteriol. 2000 Jul;182(14):4104-7. doi: 10.1128/JB.182.14.4104-4107.2000.
The expression of the neutral protease gene (npr) from the thermophilic Bacillus sp. BT1 strain was studied in its natural host and in mesophilic Bacillus subtilis. In the thermophilic BT1 strain, the transcription of the protease gene is initiated from its own promoter, just 5' to the gene. In contrast, in heterologous B. subtilis this thermophilic npr promoter does not function, and expression of the npr gene results from transcription originating upstream of an adjacent gene, open reading frame X (ORF X). A functional promoter was identified 5' to ORF X that is required for efficient expression of the npr gene in Bacillus subtilis as verified by primer extension, reverse transcription-PCR, and 5' rapid amplification of cDNA ends experiments. These data suggest that transcriptional signals used in thermophilic Bacillus sp. BT1 strain are different from those used in B. subtilis.
对嗜热芽孢杆菌BT1菌株的中性蛋白酶基因(npr)在其天然宿主及嗜温性枯草芽孢杆菌中的表达进行了研究。在嗜热BT1菌株中,蛋白酶基因的转录从其自身启动子开始,该启动子就在基因的5'端。相比之下,在异源的枯草芽孢杆菌中,这个嗜热npr启动子不起作用,npr基因的表达是由相邻基因开放阅读框X(ORF X)上游起始的转录导致的。通过引物延伸、逆转录PCR和5' cDNA末端快速扩增实验验证,在ORF X的5'端鉴定出了一个功能性启动子,它是枯草芽孢杆菌中npr基因高效表达所必需的。这些数据表明嗜热芽孢杆菌BT1菌株中使用的转录信号与枯草芽孢杆菌中使用的不同。