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首页> 外文期刊>Nucleic Acids Research >The tRNA(guanine-26,N2-N2) methyltransferase (Trm1) from the hyperthermophilic archaeon Pyrococcus furiosus: cloning, sequencing of the gene and its expression in Escherichia coli.
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The tRNA(guanine-26,N2-N2) methyltransferase (Trm1) from the hyperthermophilic archaeon Pyrococcus furiosus: cloning, sequencing of the gene and its expression in Escherichia coli.

机译:来自嗜热古菌激烈热球菌的tRNA(鸟嘌呤-26,N2-N2)甲基转移酶(Trm1):该基因的克隆,测序及其在大肠杆菌中的表达。

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摘要

The structural gene pfTRM1 (GenBank accession no. AF051912), encoding tRNA(guanine-26, N 2- N 2) methyltransferase (EC 2.1.1.32) of the strictly anaerobic hyperthermophilic archaeon Pyrococcus furiosus, has been identified by sequence similarity to the TRM1 gene of Saccharomyces cerevisiae (YDR120c). The pfTRM1 gene in a 3.0 kb restriction DNA fragment of P.furiosus genomic DNA has been cloned by library screening using a PCR probe to the 5'-part of the corresponding ORF. Sequence analysis revealed an entire ORF of 1143 bp encoding a polypeptide of 381 residues (calculated molecular mass 43.3 kDa). The deduced amino acid sequence of this newly identified gene shares significant similarity with the TRM1- like genes of three other archaea (Methanococcus jannaschii, Methanobacterium thermoautotrophicum and Archaeoglobus fulgidus), one eukaryon (Caenorhabditis elegans) and one hyperthermophilic eubacterium (Aquifex aeolicus). Two short consensus motifs for S-adenosyl-l-methionine binding are detected in the sequence of pfTrm1p. Cloning of the P.furiosus TRM1 gene in an Escherichia coli expression vector allowed expression of the recombinant protein (pfTrm1p) with an apparent molecular mass of 42 kDa. A protein extract from the transformed E.coli cells shows enzymatic activity for the quantitative formation of N 2, N 2-dimethylguanosine at position 26 in a transcript of yeast tRNAPhe used as substrate. The recombinant enzyme was also shown to modify bulk E.coli tRNAs in vivo.
机译:已经通过与TRM1的序列相似性鉴定了编码严格厌氧的超嗜热古生热球菌的tRNA(鸟嘌呤-26,N 2- N 2)甲基转移酶(EC 2.1.1.32)的结构基因pfTRM1(GenBank登录号AF051912)。酿酒酵母基因(YDR120c)。利用PCR探针通过文库筛选,将P.furiosus基因组DNA的3.0kb限制性DNA片段中的pfTRM1基因克隆到相应ORF的5'部分。序列分析显示,完整的ORF为1143 bp,编码381个残基的多肽(计算分子量43.3 kDa)。这个新鉴定的基因的推导氨基酸序列与其他三个古细菌(詹氏甲烷球菌,嗜热甲烷杆菌和粉状古细菌),一个真核生物(秀丽隐杆线虫)和一个超嗜热真细菌(Aquifex ae。在pfTrm1p的序列中检测到两个S-腺苷-1-蛋氨酸结合的短共有基序。大肠杆菌表达载体中P.furiosus TRM1基因的克隆使得重组蛋白(pfTrm1p)的表观分子量为42 kDa。来自转化的大肠杆菌细胞的蛋白质提取物显示了在用作底物的酵母tRNAPhe转录本中的位置26处定量形成N 2,N 2-二甲基鸟苷的酶活性。还显示了重组酶在体内修饰大量大肠杆菌tRNA。

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