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嗜热古菌嗜热栖热菌中S-腺苷同型半胱氨酸水解酶编码基因的克隆与测序

Cloning and sequencing of the gene coding for S-adenosylhomocysteine hydrolase in the thermophilic archaeon Sulfolobus solfataricus.

作者信息

Porcelli M, Cacciapuoti G, Fusco S, Bertoldo C, De Rosa M, Zappia V

机构信息

Istituto di Biochimica delle Macromolecole, Facoltà di Medicina e Chirurgia, Seconda Università degli Studi di Napoli, Naples, Italy.

出版信息

Gene. 1996 Oct 24;177(1-2):17-22. doi: 10.1016/0378-1119(96)00263-6.

Abstract

The gene from the thermophilic archaeon Sulfolobus solfataricus (Ss), encoding the S-adenosylhomocysteine hydrolase (AdoHcyHD), has been cloned. Two degenerate oligodeoxyribonucleotide (oligo) probes, synthesized on the basis of amino acid (aa) sequence of cyanogen bromide-peptide fragments of the purified protein, were used to screen a genomic library of Ss cloned into the pGEM7Zf(+) vector. The AdoHcyHD gene (adohcyhd) comprises 1254 nucleotides (nt) and encodes a polypeptide of 417 aa with a deduced molecular mass of 46 kDa, in good agreement with the value directly measured for the purified enzyme. The identity of more than 32% of the deduced aa sequence was confirmed by Edman degradation of peptides. Putative regulatory elements which are in good agreement with the archaeal promoter consensus sequences were identified in the flanking regions. Comparison of the aa sequences of AdoHcyHD from different sources shows a remarkable degree of conservation. Surprisingly, several aa residues, thought important in substrate binding and catalysis, show non-conserved replacements in Ss AdoHcyHD.

摘要

来自嗜热古菌嗜热栖热菌(Ss)的编码S-腺苷同型半胱氨酸水解酶(AdoHcyHD)的基因已被克隆。根据纯化蛋白的溴化氰肽片段的氨基酸(aa)序列合成了两个简并寡脱氧核糖核苷酸(oligo)探针,用于筛选克隆到pGEM7Zf(+)载体中的Ss基因组文库。AdoHcyHD基因(adohcyhd)由1254个核苷酸(nt)组成,编码一个417个aa的多肽,推导分子量为46 kDa,与纯化酶直接测得的值高度一致。通过肽的埃德曼降解证实了推导的aa序列中超过32%的一致性。在侧翼区域鉴定出与古菌启动子共有序列高度一致的假定调控元件。不同来源的AdoHcyHD的aa序列比较显示出显著的保守程度。令人惊讶的是,一些被认为在底物结合和催化中重要的aa残基在Ss AdoHcyHD中显示出非保守替代。

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