ESTM-Escola Superior de Turismo e Tecnologia do Mar, Instituto Politécnico de Leiria, Santuário N.ª Sra dos Remédios, Apartado 126, 2524-909 Peniche, Portugal.
Biotechnol Bioeng. 2010 Dec 1;107(5):753-62. doi: 10.1002/bit.22867.
There is a marked trend in pharmaceutical industry towards the replacement of classical organic methods by "green" alternatives that minimize or eliminate the generation of waste and avoid, where possible, the use of toxic and/or hazardous reagents and solvents. In this work the kinetically controlled synthesis of cephalexin by soluble and penicillin G acylase immobilized in sol-gel micro-particles with magnetic properties was performed in aqueous media with PGME and 7-ADCA as substrates, at different concentrations of substrate, temperature, pH, enzyme to substrate ratio and acyl donor to nucleophile ratio. Excess acyl donor had a strong effect on cephalexin productivity. A PGME/7-ADCA ratio of 3 was considered optimum. A maximum specific productivity of 5.9 mmol h(-1), gbiocatalyst(-1) at 160 mM 7-ADCA, 480 mM PGME and low enzyme to substrate ratio at 32.5 U mmol(-1) 7-ADCA was obtained with immobilized PGA in full aqueous medium, suggesting that diffusional limitations were minimized when compared with other commercial biocatalysts. A half-life of 133 h for the immobilized biocatalyst was estimated during cephalexin synthesis in the presence of 100 mM 7-ADCA and 300 mM PGME, in 50 mM Tris/HCl at pH 7.2 and 14°C. These results compare quite favorably with those previously reported for the kinetically controlled synthesis of cephalexin.
制药行业有一个明显的趋势,即用“绿色”替代品替代经典的有机方法,这些替代品最大限度地减少或消除了废物的产生,并尽可能避免使用有毒和/或危险的试剂和溶剂。在这项工作中,在水性介质中,使用 PGME 和 7-ADCA 作为底物,在不同的底物浓度、温度、pH 值、酶与底物的比例和酰基供体与亲核试剂的比例下,通过可溶的和固定在溶胶-凝胶微颗粒中的青霉素 G 酰化酶,对头孢氨苄进行动力学控制合成。过量的酰基供体对头孢氨苄的产率有很大的影响。PGME/7-ADCA 的比例为 3 被认为是最佳的。在 160mM 7-ADCA、480mM PGME 和低酶与底物比例(32.5Ummol(-1) 7-ADCA)下,固定化 PGA 在全水介质中获得了 5.9mmol h(-1),gbiocatalyst(-1)的最大比产率,表明与其他商业生物催化剂相比,扩散限制最小。在 100mM 7-ADCA 和 300mM PGME、50mM Tris/HCl(pH7.2)和 14°C 的存在下,固定化生物催化剂在头孢氨苄合成中的半衰期估计为 133h。这些结果与以前报道的动力学控制合成头孢氨苄的结果相当。