首页> 外文期刊>Biochimica et Biophysica Acta. General Subjects >Genes of the thymidine salvage pathway: Thymine-7-hydroxylase from a Rhodotorula glutinis cDNA library and iso-orotate decarboxylase from Neurospora crassa
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Genes of the thymidine salvage pathway: Thymine-7-hydroxylase from a Rhodotorula glutinis cDNA library and iso-orotate decarboxylase from Neurospora crassa

机译:胸苷挽救途径的基因:来自Rhodotorula glutinis cDNA文库的胸腺嘧啶7-羟化酶和来自Crus Neurospora crassa的异乳清酸脱羧酶

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Genes for two enzymes in the thymidine salvage pathway, thymine-7-hydroxylase (THase; official name thymine dioxygenase) and isoorotate decarboxylase (IDCase) have been isolated from fungal sources. THase was isolated from a Rhodotorula glutinis cDNA library using a degenerate oligonucleotide based on the published amino acid sequence. The coding sequence was transferred to an Escherichia coli expression system, from which recombinant THase activity was measured using C-14-labeled thymine. The THase sequence shows an almost complete avoidance of codons ending in A or T: 95.8% GC content is present in the third position of codons. A connection between this codon bias and the role of the thymidine salvage pathway in pyrimidine metabolism is proposed. The THase sequence is similar to Group I Fe+2-dependent, alpha KG-dependent dioxygenases. The R. glutinis THase gene was used to locate the probable THase genes in the sequenced genomes of Neurospora crassa and Aspergillus nidulans. The genes neighboring THase in these two genomes are similar to each other, and are similar to the mammalian 2-amino-3-carboxymuconate-6-semialdhyde decarboxylase (ACMSD), leading to their identification as IDCase genes. The N. crassa version was isolated by PCR of genomic DNA, and IDCase activity was measured in recombinant E. coli carrying this gene. A new family of decarboxylases, using similar substrates, is identified by virtue of the protein sequence similarity. (c) 2005 Elsevier B.V. All rights reserved.
机译:已从真菌来源中分离出胸苷挽救途径中两种酶的基因,胸腺嘧啶7-羟化酶(THase;正式名称胸腺嘧啶二加氧酶)和异旋酸脱羧酶(IDCase)。使用简并的​​寡核苷酸基于已公开的氨基酸序列从红假单胞菌的glutinis cDNA文库中分离出THase。将编码序列转移到大肠杆菌表达系统中,使用C-14标记的胸腺嘧啶测定重组THase活性。 THase序列显示几乎完全避免了以A或T结尾的密码子:密码子的第三位存在95.8%的GC含量。提出了这种密码子偏倚与嘧啶清除途径在嘧啶代谢中的作用之间的联系。 THase序列类似于第I组Fe + 2依赖性,αKG依赖性双加氧酶。谷氨酸棒杆菌THase基因用于在拟南芥和构巢曲霉的测序基因组中定位可能的THase基因。这两个基因组中邻近THase的基因彼此相似,并且与哺乳动物的2-氨基-3-羧基粘康酸酯-6-二醛脱羧酶(ACMSD)相似,从而被鉴定为IDCase基因。通过基因组DNA的PCR分离了猪笼草的N. crassa版本,并在携带该基因的重组大肠杆菌中测量了IDCase活性。利用相似的底物,通过蛋白质序列相似性鉴定了一个新的脱羧酶家族。 (c)2005 Elsevier B.V.保留所有权利。

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