Alduina Rosa, Gallo Giuseppe
Department of Science and Molecular and Biomolecular Technology, University of Palermo, Viale delle Scienze, 90128 Palermo, Italy.
J Biomed Biotechnol. 2012;2012:462049. doi: 10.1155/2012/462049. Epub 2012 Aug 7.
Actinomycetes are an important source of biologically active compounds, like antibiotics, antitumor agents, and immunosuppressors. Genome sequencing is revealing that this class of microorganisms has larger genomes relative to other bacteria and uses a considerable fraction of its coding capacity (5-10%) for the production of mostly cryptic secondary metabolites. To access actinomycetes biosynthetic capabilities or to improve the pharmacokinetic properties and production yields of these chemically complex compounds, genetic manipulation of the producer strains can be performed. Heterologous expression in amenable hosts can be useful to exploit and to explore the genetic potential of actinomycetes and not cultivable but interesting bacteria. Artificial chromosomes that can be stably integrated into the Streptomyces genome were constructed and demonstrated to be effective for transferring entire biosynthetic gene clusters from intractable actinomycetes into more suitable hosts. In this paper, the construction of several shuttle Escherichia coli-Streptomyces artificial chromosomes is discussed together with old and new strategies applied to improve heterologous production of secondary metabolites.
放线菌是生物活性化合物的重要来源,如抗生素、抗肿瘤剂和免疫抑制剂。基因组测序表明,这类微生物的基因组相对于其他细菌更大,并且其相当一部分编码能力(5-10%)用于产生大多为隐秘的次级代谢产物。为了挖掘放线菌的生物合成能力,或改善这些化学结构复杂的化合物的药代动力学性质及产量,可以对生产菌株进行基因操作。在合适的宿主中进行异源表达,有助于开发和探索放线菌以及不可培养但有趣的细菌的遗传潜力。已构建出能够稳定整合到链霉菌基因组中的人工染色体,并证明其可有效地将完整的生物合成基因簇从难处理的放线菌转移到更合适的宿主中。本文讨论了几种大肠杆菌-链霉菌穿梭人工染色体的构建,以及应用于提高次级代谢产物异源产量的新旧策略。