Ammendola S, Raia C A, Caruso C, Camardella L, D'Auria S, De Rosa M, Rossi M
Istituto di Biochimica delle Proteine ed Enzimologia, CNR, Napoli, Italy.
Biochemistry. 1992 Dec 15;31(49):12514-23. doi: 10.1021/bi00164a031.
The NAD(+)-dependent alcohol dehydrogenase (EC 1.1.1.1) from the thermoacidophilic archaebacterium Sulfolobus solfataricus, DSM1617 strain (SSADH), has been purified and characterized. Its gene has been isolated by screening two S. Solfataricus genomic libraries using oligonucleotide probes. The encoding sequence consists of 1041 base pairs, and it shows a high preference for codons ending in T or A. The primary structure, determined by peptide and gene analysis, consists of 347 amino acid residues, yielding a molecular weight of 37,588. A level of identity of 24-25% was found with the amino acid sequences of horse liver, yeast, and Thermoanaerobium brockii alcohol dehydrogenases. The coenzyme-binding and catalytic and structural zinc-binding residues typical of eukaryotic alcohol dehydrogenases were found in SSADH with the difference that one out of the four structural zinc-binding Cys residues is substituted by Glu. The protein contains four zinc atoms per dimer, two of which are removed by chelating agents with a concomitant loss of structural stability.
来自嗜热嗜酸古细菌嗜热栖热菌DSM1617菌株(SSADH)的NAD(+)依赖性乙醇脱氢酶(EC 1.1.1.1)已被纯化并进行了特性分析。通过使用寡核苷酸探针筛选两个嗜热栖热菌基因组文库,分离出了其基因。编码序列由1041个碱基对组成,并且对以T或A结尾的密码子具有高度偏好性。通过肽和基因分析确定的一级结构由347个氨基酸残基组成,分子量为37,588。发现与马肝、酵母和布氏嗜热厌氧菌乙醇脱氢酶的氨基酸序列具有24% - 25%的同一性。在SSADH中发现了真核乙醇脱氢酶典型的辅酶结合、催化和结构锌结合残基,不同之处在于四个结构锌结合半胱氨酸残基中的一个被谷氨酸取代。该蛋白质每个二聚体含有四个锌原子,其中两个被螯合剂去除,同时结构稳定性丧失。