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首页> 外文期刊>Applied and Environmental Microbiology >Cloning, Sequencing, and Expression of the Cold-Inducible hutU Gene from the Antarctic Psychrotrophic Bacterium Pseudomonas syringae
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Cloning, Sequencing, and Expression of the Cold-Inducible hutU Gene from the Antarctic Psychrotrophic Bacterium Pseudomonas syringae

机译:南极精神营养细菌丁香假单胞菌的冷诱导性hutU基因的克隆,测序和表达

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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° 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°C) and that there is more than one transcription initiation site. One of the initiation sites was specific to the cells grown at 4°C, which was different from the common initiation sites observed at both 4 and 22°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 (GXGX2GX10G) 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.
机译:使用基于Tn 5的启动子探针载体进行的启动子融合研究更早地发现,在较低温度(4°C)的南极精神营养细菌丁香假单胞菌中,编码组氨酸利用途径尿酸酶的hutU基因被上调。为了检查来自精神营养菌的尿素酶基因及其启动子元件的特性,在本研究中克隆,测序和分析了丁香假单胞菌的完整hutU及其上游区域。 Northern杂交和引物延伸分析表明,温度下降(22至4°C)时,hutU基因是可诱导的,并且存在多个转录起始位点。起始位点之一对在4°C下生长的细胞具有特异性,这与在4和22°C下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没有观察到典型的启动子共有序列,但是在启动子的α10位置有特征性的CAAAA序列。此外,转录和翻译起始位点的位置表明hutU mRNA包含一个长的5'非翻译区,这是许多嗜温细菌的冷诱导基因的特征。比较各种细菌(包括嗜温和嗜营养的假单胞菌属)的尿素酶的氨基酸序列,表明这些酶之间具有高度相似性。酶序列包含罗斯曼折叠的签名基序(GXGX2GX10G),用于二核苷酸(NAD +)结合以及活性位点内和周围两个保守的半胱氨酸残基。然而,精神营养酶具有延伸的N-末端。

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