Department of Molecular Microbiology, John Innes Centre, Colney Lane, Norwich, NR5 7UH, UK.
Heredity (Edinb). 2019 Jul;123(1):23-32. doi: 10.1038/s41437-019-0196-0. Epub 2019 Jun 12.
Sixty years ago, the actinomycetes, which include members of the genus Streptomyces, with their bacterial cellular dimensions but a mycelial growth habit like fungi, were generally regarded as a possible intermediate group, and virtually nothing was known about their genetics. We now know that they are bacteria, but with many original features. Their genome is linear with a unique mode of replication, not circular like those of nearly all other bacteria. They transfer their chromosome from donor to recipient by a conjugation mechanism, but this is radically different from the E. coli paradigm. They have twice as many genes as a typical rod-shaped bacterium like Escherichia coli or Bacillus subtilis, and the genome typically carries 20 or more gene clusters encoding the biosynthesis of antibiotics and other specialised metabolites, only a small proportion of which are expressed under typical laboratory screening conditions. This means that there is a vast number of potentially valuable compounds to be discovered when these 'sleeping' genes are activated. Streptomyces genetics has revolutionised natural product chemistry by facilitating the analysis of novel biosynthetic steps and has led to the ability to engineer novel biosynthetic pathways and hence 'unnatural natural products', with potential to generate lead compounds for use in the struggle to combat the rise of antimicrobial resistance.
六十年前,放线菌(包括链霉菌属成员)被普遍认为是一种可能的中间群,它们具有细菌的细胞尺寸,但却具有真菌那样的菌丝体生长习性,而且人们对其遗传学几乎一无所知。我们现在知道它们是细菌,但具有许多原始特征。它们的基因组是线性的,具有独特的复制方式,不像几乎所有其他细菌那样是圆形的。它们通过一种接合机制将染色体从供体转移到受体,而这种机制与大肠杆菌的模式完全不同。它们的基因数量是典型杆状细菌(如大肠杆菌或枯草芽孢杆菌)的两倍,基因组通常携带 20 个或更多基因簇,这些基因簇编码抗生素和其他特殊代谢物的生物合成,只有一小部分在典型的实验室筛选条件下表达。这意味着,当这些“休眠”基因被激活时,将会有大量潜在有价值的化合物有待发现。链霉菌遗传学通过促进对新生物合成步骤的分析,彻底改变了天然产物化学,并使构建新型生物合成途径以及“非天然天然产物”成为可能,这可能为对抗抗菌药物耐药性的兴起而产生先导化合物提供了潜力。