Mitousis Lena, Thoma Yvonne, Musiol-Kroll Ewa M
Interfaculty Institute for Microbiology and Infection Medicine Tübingen (IMIT), Microbiology/Biotechnology, University of Tübingen, Auf der Morgenstelle 28, 72076 Tübingen, Germany.
Antibiotics (Basel). 2020 Aug 8;9(8):494. doi: 10.3390/antibiotics9080494.
The first antibiotic-producing actinomycete () was described by Waksman and Woodruff in 1940. This discovery initiated the "actinomycetes era", in which several species were identified and demonstrated to be a great source of bioactive compounds. However, the remarkable group of microorganisms and their potential for the production of bioactive agents were only partially exploited. This is caused by the fact that the growth of many actinomycetes cannot be reproduced on artificial media at laboratory conditions. In addition, sequencing, genome mining and bioactivity screening disclosed that numerous biosynthetic gene clusters (BGCs), encoded in actinomycetes genomes are not expressed and thus, the respective potential products remain uncharacterized. Therefore, a lot of effort was put into the development of technologies that facilitate the access to actinomycetes genomes and activation of their biosynthetic pathways. In this review, we mainly focus on molecular tools and methods for genetic engineering of actinomycetes that have emerged in the field in the past five years (2015-2020). In addition, we highlight examples of successful application of the recently developed technologies in genetic engineering of actinomycetes for activation and/or improvement of the biosynthesis of secondary metabolites.
1940年,瓦克斯曼和伍德拉夫描述了第一种产生抗生素的放线菌()。这一发现开启了“放线菌时代”,在此期间,几种放线菌被鉴定出来,并被证明是生物活性化合物的重要来源。然而,这类卓越的微生物及其产生生物活性剂的潜力仅得到了部分开发。这是因为许多放线菌在实验室条件下无法在人工培养基上繁殖。此外,测序、基因组挖掘和生物活性筛选表明,放线菌基因组中编码的众多生物合成基因簇(BGCs)并未表达,因此,相应的潜在产物仍未得到表征。因此,人们投入了大量精力来开发有助于获取放线菌基因组并激活其生物合成途径的技术。在本综述中,我们主要关注过去五年(2015 - 2020年)该领域出现的用于放线菌基因工程的分子工具和方法。此外,我们还重点介绍了最近开发的技术在放线菌基因工程中成功应用的实例,这些应用旨在激活和/或改善次生代谢产物的生物合成。