Piepersberg W
Department of Microbiology, BUGH Wuppertal, Germany.
Crit Rev Biotechnol. 1994;14(3):251-85. doi: 10.3109/07388554409079835.
Actinomycetes represent the microbial group richest in production of variable secondary metabolites. These mostly bioactive molecules are the end products of complex multistep biosynthetic pathways. Recent progress in the molecular genetics and biochemistry of the biosynthetic capacities of actinomycetes enables first attempts to redesign these pathways in a directed fashion. However, in contrast to several examples of designed biochemical improvement of primary metabolic processes in microorganisms, none of the products or strains derived from pathway engineering in actinomycetes discussed herein have reached pilot or production scale. The main reasons for this slow progress are the complicated pathways themselves, their complex regulation during the actinomycete cell cycle, and their uniqueness, as most pathways and products are specific for a strain rather than for a given species or larger taxonomic group. However, the modular use of a minimum of very similar enzymes and their conversion of similar intermediates to form the building blocks for the production of a maximum of divergent end products gives hope for the future application of these genetic models for the redesign of complex pathways for modified or new natural products. Several strategies that can be followed to reach this aim are discussed, mainly for the variable 6-deoxyhexose metabolism as an ubiquitously applicable example.
放线菌是产生多样次级代谢产物最为丰富的微生物类群。这些大多具有生物活性的分子是复杂多步生物合成途径的终产物。放线菌生物合成能力的分子遗传学和生物化学方面的最新进展使得人们首次尝试以定向方式重新设计这些途径。然而,与微生物中初级代谢过程经设计后的生化改进的几个例子不同,本文讨论的源自放线菌途径工程的产物或菌株均未达到中试或生产规模。进展缓慢的主要原因在于途径本身复杂、在放线菌细胞周期中调控复杂以及其独特性,因为大多数途径和产物是菌株特异性的,而非特定物种或更大分类群所共有。然而,最少数量的非常相似的酶的模块化使用以及它们将相似中间体转化为构建模块以产生最多样化的终产物,为这些遗传模型未来用于重新设计复杂途径以生产修饰的或新的天然产物带来了希望。文中讨论了为实现这一目标可采用的几种策略,主要以普遍适用的6 - 脱氧己糖代谢为例。