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Nucleoside 2'-Deoxyribosyltransferase from psychrophilic bacterium bacillus psychrosaccharolyticus - Preparation of an immobilized biocatalyst for the enzymatic synthesis of therapeutic nucleosides

机译:嗜冷细菌解毒芽孢杆菌的核苷2'-脱氧核糖基转移酶-固定化生物催化剂的制备,用于酶法合成治疗性核苷

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摘要

Nucleoside 2'-deoxyribosyltransferase (NDT) from the psychrophilic bacterium Bacillus psychrosaccharolyticus CECT 4074 has been cloned and produced for the first time. A preliminary characterization of the recombinant protein indicates that the enzyme is an NDT type II since it catalyzes the transfer of 2'-deoxyribose between purines and pyrimidines. The enzyme (BpNDT) displays a high activity and stability in a broad range of pH and temperature. In addition, different approaches for the immobilization of BpNDT onto several supports have been studied in order to prepare a suitable biocatalyst for the one-step industrial enzymatic synthesis of different therapeutic nucleosides. Best results were obtained by adsorbing the enzyme on PEI-functionalized agarose and subsequent cross-linking with aldehyde-dextran (20 kDa and 70% oxidation degree). The immobilized enzyme could be recycled for at least 30 consecutive cycles in the synthesis of 2'-deoxyadenosine from 2'-deoxyuridine and adenine at 37 °C and pH 8.0, with a 25% loss of activity. High conversion yield of trifluridine (64.4%) was achieved in 2 h when 20 mM of 2'-deoxyuridine and 10 mM 5-trifluorothymine were employed in the transglycosylation reaction catalyzed by immobilized BpNDT at 37 °C and pH 7.5.
机译:首次克隆并生产了来自嗜冷细菌芽孢杆菌Bacillus psychrosaccharolyticus CECT 4074的核苷2'-脱氧核糖基转移酶(NDT)。重组蛋白的初步表征表明该酶为NDT II型,因为它催化2'-脱氧核糖在嘌呤和嘧啶之间的转移。该酶(BpNDT)在很宽的pH和温度范围内均显示出高活性和稳定性。此外,已经研究了将BpNDT固定在几种载体上的不同方法,以便为不同的治疗性核苷的一步工业酶法合成制备合适的生物催化剂。通过将酶吸附到PEI-官能化的琼脂糖上并随后与醛-葡聚糖交联(20 kDa和70%氧化度)获得最佳结果。固定化的酶可以在37°C和pH 8.0下由2'-脱氧尿苷和腺嘌呤合成2'-脱氧腺苷的过程中至少循环使用30个连续循环,活性降低25%。当在37°C和pH 7.5下固定BpNDT催化转糖基化反应中使用20 mM的2'-脱氧尿苷和10 mM的5-三氟胸腺嘧啶反应时,三氟吡啶的转化率较高(64.4%)。

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