人工M374 Arg和M374 Lys突变体中酪氨酸酶多巴氧化酶活性的丧失

Roudabeh Behzadi Andouhjerdi, M. Sadeghizadeh
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引用次数: 0

摘要

酪氨酸酶(Ec: 1.14.18.1)是一种含铜酶,广泛存在于原核生物、真核生物、哺乳动物、无脊椎动物和植物等生命的各个领域。酪氨酸酶催化单酚氧化为二酚和二酚氧化为邻醌。酪氨酸酶结晶学数据显示了两个组氨酸丰富的区域,称为CuA和CuB。含有残基M374, S375和V377的环路连接CuA和CuB中心。这个环对酶的稳定性至关重要。本研究采用定点诱变技术,用精氨酸和赖氨酸替代M374。克隆于pET 28b(+)的合成cDNA。这些突变不影响组氨酸367(H367)侧链的方向,导致活性丧失。
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Loss of Human Tyrosinase DOPA Oxidase Activity in Artificial M374 Arg and M 374 Lys Mutants
Tyrosinase (Ec: 1.14.18.1) is a copper - containing enzyme which is distributed in all domains of life such as prokaryote, eukaryote, mammals, invertebrates and plants. Tyrosinase catalyzes the oxidation of monophenols to diphenols and diphenols to o-quinones . The tyrosinase crystallographic data shows two histidine -rich regions named CuA and CuB. A loop containing residues M374, S375 and V377 connects the CuA and CuB Centers. This loop is essential for stability of the enzyme. In this study, site directed mutagenesis was used for the replacement of M374 by Arginine and Lysine.in synthesized cDNA cloned in pET 28b (+) . These mutations don't affect the orientation of the Histidin 367(H367) side chain, resulting in loss of activity.
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