Liu X, Taber H W
Department of Microbiology, Immunology, and Molecular Genetics, Albany Medical College, Albany, New York 12201, USA.
J Bacteriol. 1998 Dec;180(23):6154-63. doi: 10.1128/JB.180.23.6154-6163.1998.
Bacillus subtilis cytochrome c oxidase caa3 is encoded by the ctaCDEF genes at the ctaABCDEF locus, with the ctaBCDEF genes organized as an operon-like unit. A dyad symmetry sequence and a catabolite response element homolog can be recognized in the 240-bp intercistronic region between ctaB and ctaC. ctaB'-lacZ and ctaBCD'-lacZ transcriptional fusions integrated at the native locus were used to study catabolite effects on transcription of the ctaB and ctaCDEF genes. In Schaeffer's medium lacking glucose, ctaBCD'-lacZ was expressed at a very low level during the exponential phase, and expression increased about 30-fold 2 h after entry into the stationary phase. In the presence of 0.5% glucose, ctaBCD'-lacZ expression was totally repressed. In contrast to ctaBCD'-lacZ, ctaB'-lacZ was constitutively expressed regardless of carbon source. The ctaCDEF genes were separated from ctaB by insertion of plasmids carrying selectable markers in such a way that the ctaCDEF and ctaB transcription units remained intact. Enzymatic assays of caa3 with these constructs, showed that ctaCDEF was not expressed independently of ctaB. Also, when a 'ctaB-ctaC'-lacZ fusion (containing the ctaB-ctaC intercistronic region) was placed at a remote nonessential locus, beta-galactosidase activity could not be detected. The absence of a promoter in the ctaB-ctaC intercistronic space also was indicated by the inability to detect ctaC-specific transcripts with RNase protection assays, primer extension, and rapid amplification of 5' cDNA ends. Direct mRNA measurements showed that, in the presence of 0.5% glucose, ctaBCDEF transcripts terminated at the 3' end of the putative stem-loop structure and the distal portion was down-regulated. A possible mechanism for ctaCDEF gene regulation is suggested. Catabolite repression of ctaBCD'-lacZ was partly dependent on CcpA but was independent of HPr. The expression of ctaBCDEF also appears to require the strC, ctaA, and resD-resE gene products.
枯草芽孢杆菌细胞色素c氧化酶caa3由ctaABCDEF位点的ctaCDEF基因编码,其中ctaBCDEF基因组成一个类似操纵子的单元。在ctaB和ctaC之间240bp的基因间区域可识别出一个二元对称序列和一个分解代谢物反应元件同源物。整合在天然位点的ctaB'-lacZ和ctaBCD'-lacZ转录融合体用于研究分解代谢物对ctaB和ctaCDEF基因转录的影响。在缺乏葡萄糖的Schaeffer培养基中,ctaBCD'-lacZ在指数期表达水平很低,进入稳定期2小时后表达增加约30倍。在0.5%葡萄糖存在的情况下,ctaBCD'-lacZ的表达完全被抑制。与ctaBCD'-lacZ不同,ctaB'-lacZ无论碳源如何均组成性表达。通过携带选择标记的质粒插入,使ctaCDEF基因与ctaB分离,使得ctaCDEF和ctaB转录单元保持完整。用这些构建体对caa3进行酶活性测定表明,ctaCDEF不能独立于ctaB表达。此外,当一个“ctaB-ctaC”-lacZ融合体(包含ctaB-ctaC基因间区域)置于一个遥远的非必需位点时,无法检测到β-半乳糖苷酶活性。通过核糖核酸酶保护分析、引物延伸和5' cDNA末端快速扩增无法检测到ctaC特异性转录本,这也表明ctaB-ctaC基因间区域不存在启动子。直接的mRNA测量表明,在0.5%葡萄糖存在的情况下,ctaBCDEF转录本在假定的茎环结构的3'末端终止,远端部分表达下调。提出了一种ctaCDEF基因调控的可能机制。ctaBCD'-lacZ的分解代谢物阻遏部分依赖于CcpA,但不依赖于HPr。ctaBCDEF的表达似乎也需要strC、ctaA以及resD-resE基因产物。