Janiyani Kamala L, Ray M K
Centre for Cellular and Molecular Biology, Hyderabad 500 007, India.
Appl Environ Microbiol. 2002 Jan;68(1):1-10. doi: 10.1128/AEM.68.1.1-10.2002.
A promoter-fusion study with a Tn 5-based promoter probe vector had earlier found that the hutU gene which encodes the enzyme urocanase for the histidine utilization pathway is upregulated at a lower temperature (4 degrees C) in the Antarctic psychrotrophic bacterium Pseudomonas syringae. To examine the characteristics of the urocanase gene and its promoter elements from the psychrotroph, the complete hutU and its upstream region from P. syringae were cloned, sequenced, and analyzed in the present study. Northern blot and primer extension analyses suggested that the hutU gene is inducible upon a downshift of temperature (22 to 4 degrees C) and that there is more than one transcription initiation site. One of the initiation sites was specific to the cells grown at 4 degrees C, which was different from the common initiation sites observed at both 4 and 22 degrees C. Although no typical promoter consensus sequences were observed in the flanking region of the transcription initiation sites, there was a characteristic CAAAA sequence at the -10 position of the promoters. Additionally, the location of the transcription and translation initiation sites suggested that the hutU mRNA contains a long 5'-untranslated region, a characteristic feature of many cold-inducible genes of mesophilic bacteria. A comparison of deduced amino acid sequences of urocanase from various bacteria, including the mesophilic and psychrotrophic Pseudomonas spp., suggests that there is a high degree of similarity between the enzymes. The enzyme sequence contains a signature motif (GXGX(2)GX(10)G) of the Rossmann fold for dinucleotide (NAD(+)) binding and two conserved cysteine residues in and around the active site. The psychrotrophic enzyme, however, has an extended N-terminal end.
一项使用基于Tn 5的启动子探针载体的启动子融合研究早些时候发现,编码组氨酸利用途径中尿刊酸酶的hutU基因在南极嗜冷细菌丁香假单胞菌中,于较低温度(4℃)下会上调。为了研究来自该嗜冷菌的尿刊酸酶基因及其启动子元件的特性,在本研究中克隆、测序并分析了丁香假单胞菌完整的hutU基因及其上游区域。Northern印迹和引物延伸分析表明,hutU基因在温度下降(从22℃降至4℃)时可被诱导,且存在多个转录起始位点。其中一个起始位点是4℃生长的细胞所特有的,这与在4℃和22℃均观察到的常见起始位点不同。尽管在转录起始位点的侧翼区域未观察到典型的启动子共有序列,但在启动子的-10位置有一个特征性的CAAAA序列。此外,转录和翻译起始位点的位置表明,hutU mRNA含有一个长的5'非翻译区,这是许多嗜温细菌的冷诱导基因的一个特征。对包括嗜温和嗜冷假单胞菌属在内的各种细菌的尿刊酸酶推导氨基酸序列进行比较,表明这些酶之间具有高度相似性。该酶序列包含一个用于二核苷酸(NAD(+))结合的Rossmann折叠的特征基序(GXGX(2)GX(10)G)以及活性位点内和周围的两个保守半胱氨酸残基。然而,嗜冷酶具有延伸的N末端。