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青霉素 G 酰化酶为基础的生物催化的现状与展望。

Current state and perspectives of penicillin G acylase-based biocatalyses.

机构信息

Laboratory of Enzyme Technology, Institute of Microbiology v.v.i., Academy of Sciences of the Czech Republic, Vídeňská 1083, 14220, Prague 4, Czech Republic.

出版信息

Appl Microbiol Biotechnol. 2014 Apr;98(7):2867-79. doi: 10.1007/s00253-013-5492-7. Epub 2014 Jan 21.

Abstract

In the course of more than 60-year history, penicillin G acylase (PGA) gained a unique position among enzymes used by pharmaceutical industry for production of β-lactam antibiotics. Kinetically controlled enzymatic syntheses of cephalosporins of novel generations in which PGA catalyzes coupling of activated acyl donor with nucleophile belong among the latest large-scale applications. Contrary to rather specific roles of other enzymes involved in β-lactam biocatalyses, the PGA seems to have the greatest potential. On the laboratory scale, other applications with industrial potential were described, e.g., directed evolution of the enzyme to meet specific demands of industrial processes or its modification into the enzyme catalyzing reactions with novel substrates. The fact that β-lactams represent the most important group of antibiotics comprising 65 % of the world antibiotic market explains such a tremendous and continuous interest in this enzyme. Indeed, the annual consumption of PGA has recently been estimated to range from 10 to 30 million tons. The application potential of the enzyme goes beyond the β-lactam biocatalysis due to its enantioselectivity and promiscuity: the PGA can be used for the production of achiral and chiral compounds convenient for the preparation of synthons and active pharmaceutical ingrediences, respectively. These biocatalyses, however, still wait for large-scale application.

摘要

在超过 60 年的历史进程中,青霉素 G 酰化酶(PGA)在制药工业用于生产β-内酰胺抗生素的酶中占据了独特的地位。动力学控制的新型头孢菌素的酶促合成,其中 PGA 催化活性酰基供体与亲核试剂的偶联,属于最新的大规模应用之一。与参与β-内酰胺生物催化的其他酶的相当具体的作用相反,PGA 似乎具有最大的潜力。在实验室规模上,还描述了其他具有工业潜力的应用,例如,酶的定向进化以满足工业过程的特定需求或修饰为催化具有新型底物的反应的酶。β-内酰胺类抗生素是世界抗生素市场中最重要的抗生素,占 65%,这一事实解释了人们对这种酶的巨大而持续的兴趣。事实上,最近估计 PGA 的年消耗量在 1000 万至 3000 万吨之间。由于其对映选择性和混杂性,该酶的应用潜力超出了β-内酰胺生物催化:PGA 可用于生产非手性和手性化合物,分别方便地制备前体和活性药物成分。然而,这些生物催化仍有待大规模应用。

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