Pharmaceutical Biology and Biotechnology, Institute of Pharmaceutical Sciences, Albert-Ludwigs University, Freiburg, Germany.
Pharmaceutical Bioinformatics, Institute of Pharmaceutical Sciences, Albert-Ludwigs University, Freiburg, Germany.
J Biotechnol. 2019 Feb 20;292:23-31. doi: 10.1016/j.jbiotec.2018.12.016. Epub 2019 Jan 11.
Streptomyces asterosporus DSM 41452 is a producer of the polyketide annimycin and the non-ribosomal depsipeptide WS9326A. This strain is also notable for exhibiting a bald phenotype that is devoid of spores and aerial mycelium when grown on solid media. Based on the similarity of the 16S rRNA sequence to Streptomyces calvus, the only known producer of the fluorometabolite nucleocidin, the genome of S. asterosporus DSM 41452 was sequenced and analyzed. Twenty-nine natural product gene clusters were detected in the genome, including a gene cluster predicted to encode the fluorometabolite nucleocidin. Through genome analysis and gene complementation experiments, we demonstrate that the bald phenotype arises from a transposon gene inserted within the promoter sequence for the pleiotropic regulator adpA. Complementation of S. asterosporus DSM 41452 with a functional adpA sequence restored morphological differentiation and promoted the production of nucleocidin.
棘孢小单孢菌 DSM 41452 是聚酮类安密霉素和非核糖体衍生肽 WS9326A 的产生菌。该菌株在固体培养基上生长时表现出光秃表型,缺乏孢子和气生菌丝,这一点也很引人注目。基于 16S rRNA 序列与已知产生氟代谢物核菌素的棘孢小单孢菌 calvus 的相似性,对棘孢小单孢菌 DSM 41452 的基因组进行了测序和分析。在基因组中检测到 29 个天然产物基因簇,包括一个预测编码氟代谢物核菌素的基因簇。通过基因组分析和基因互补实验,我们证明光秃表型是由转座子基因插入多效调控因子 adpA 的启动子序列引起的。用功能正常的 adpA 序列互补 S. asterosporus DSM 41452 恢复了形态分化,并促进了核菌素的产生。