Molecular Cell Biology, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), Kluyver Center for Genomics of Industrial Fermentation, University of Groningen, The Netherlands.
Biotechnol Genet Eng Rev. 2010;27:1-32. doi: 10.1080/02648725.2010.10648143.
β-lactam antibiotics (e.g. penicillins, cephalosporins) are of major clinical importance and contribute to over 40% of the total antibiotic market. These compounds are produced as secondary metabolites by certain actinomycetes and filamentous fungi (e.g. Penicillium, Aspergillus and Acremonium species). The industrial producer of penicillin is the fungus Penicillium chrysogenum. The enzymes of the penicillin biosynthetic pathway are well characterized and most of them are encoded by genes that are organized in a cluster in the genome. Remarkably, the penicillin biosynthetic pathway is compartmentalized: the initial steps of penicillin biosynthesis are catalyzed by cytosolic enzymes, whereas the two final steps involve peroxisomal enzymes. Here, we describe the biochemical properties of the enzymes of β-lactam biosynthesis in P. chrysogenum and the role of peroxisomes in this process. An overview is given on strain improvement programs via classical mutagenesis and, more recently, genetic engineering, leading to more productive strains. Also, the potential of using heterologous hosts for the development of novel ß-lactam antibiotics and non-ribosomal peptide synthetase-based peptides is discussed.
β-内酰胺类抗生素(如青霉素类、头孢菌素类)具有重要的临床意义,占抗生素总市场的 40%以上。这些化合物是某些放线菌和丝状真菌(如青霉属、曲霉属和枝顶孢属)作为次级代谢产物产生的。青霉素的工业生产者是真菌产黄青霉。青霉素生物合成途径的酶具有很好的特征,其中大多数由基因编码,这些基因在基因组中组织成一个簇。值得注意的是,青霉素生物合成途径是分隔的:青霉素生物合成的初始步骤由胞质酶催化,而最后两个步骤涉及过氧化物酶体酶。本文描述了产黄青霉中β-内酰胺生物合成酶的生化特性以及过氧化物体在该过程中的作用。概述了通过经典诱变和最近的遗传工程进行的菌株改良计划,这些计划导致了更具生产力的菌株。还讨论了利用异源宿主开发新型β-内酰胺抗生素和基于非核糖体肽合成酶的肽的潜力。