Bridget Adzemye Fovennso, Budhathoki Rabin, Huo Chen, Joshi Soniya, Parajuli Niranjan, Sohng Jae Kyung, Kim Ki Hyun
Department of Life Science and Biochemical Engineering, Institute of Biomolecule Reconstruction (iBR), Sun Moon University, Asan, 31460, Republic of Korea.
Central Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, 44618, Nepal.
Arch Pharm Res. 2025 Jun 17. doi: 10.1007/s12272-025-01553-1.
Saccharopolyspora spinosa, a member of the Pseudonocardiaceae family, was originally isolated from soil in the Virgin Islands and is renowned for producing spinosad, a broad-spectrum insecticidal secondary metabolite. While research on S. spinosa has historically focused on spinosad production, little is known about the broader spectrum of secondary metabolites encoded by its genome. Like Streptomyces, S. spinosa harbors numerous biosynthetic gene clusters (BGCs), many of which remain cryptic under standard laboratory conditions. In this study, the spinosyn gene cluster was deleted using the heat-sensitive vector pKC1139, generating the mutant strain S. spinosaΔSPN. The fermentation products of both the wild-type S. spinosa (B1) and S. spinosaΔSPN (B2) were analyzed through HPLC coupled with high-resolution tandem mass spectrometry (HRMS/MS). Data analysis was conducted using GNPS-based molecular networking and MestReNova. A total of seven metabolites were putatively annotated in the wild-type strain (B1), with spinosyns being the predominant compounds. In contrast, the mutant strain (B2) produced putatively linear and cyclic lipopeptides, including gageostatins and gageopeptins as the major metabolites. Additionally, the crude extract from S. spinosaΔSPN (B2) exhibited antibacterial activity, likely due to the production of lipopeptides, which are known for their antimicrobial properties. These findings indicate that deletion of the spinosyn gene cluster can activate cryptic biosynthetic pathways, leading to the discovery of novel bioactive compounds with potential applications in medicine.
多刺糖多孢菌是假诺卡氏菌科的一员,最初是从美属维尔京群岛的土壤中分离出来的,以产生多杀菌素而闻名,多杀菌素是一种广谱杀虫次生代谢产物。虽然对多刺糖多孢菌的研究历来集中在多杀菌素的生产上,但对其基因组编码的更广泛的次生代谢产物了解甚少。与链霉菌一样,多刺糖多孢菌含有许多生物合成基因簇(BGCs),其中许多在标准实验室条件下仍处于沉默状态。在本研究中,使用热敏载体pKC1139删除了多杀菌素基因簇,产生了突变菌株多刺糖多孢菌ΔSPN。通过高效液相色谱(HPLC)结合高分辨率串联质谱(HRMS/MS)分析了野生型多刺糖多孢菌(B1)和多刺糖多孢菌ΔSPN(B2)的发酵产物。使用基于全球天然产物社会分子网络(GNPS)的分子网络和MestReNova进行数据分析。在野生型菌株(B1)中总共推定注释了七种代谢产物,其中多杀菌素是主要化合物。相比之下,突变菌株(B2)产生了推定的线性和环状脂肽,包括静菌定素和静肽菌素作为主要代谢产物。此外,多刺糖多孢菌ΔSPN(B2)的粗提物表现出抗菌活性,这可能是由于产生了具有抗菌特性的脂肽。这些发现表明,删除多杀菌素基因簇可以激活隐藏的生物合成途径,从而发现具有医学潜在应用的新型生物活性化合物。