Liang Libang, Sproule Amanda, Haltli Brad, Marchbank Douglas H, Berrué Fabrice, Overy David P, McQuillan Kate, Lanteigne Martin, Duncan Noelle, Correa Hebelin, Kerr Russell G
Department of Chemistry, University of Prince Edward Island, Charlottetown, PE, Canada.
Department of Biomedical Sciences, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PE, Canada.
Front Microbiol. 2019 Jan 17;9:3351. doi: 10.3389/fmicb.2018.03351. eCollection 2018.
Herein we describe a modified bacterial culture methodology as a tool to discover new natural products via supplementing actinomycete fermentation media with autoclaved cultures of "inducer" microbes. Using seven actinomycetes and four inducer microbes, we detected 28 metabolites that were induced in UHPLC-HRESIMS-based analysis of bacterial fermentations. Metabolomic analysis indicated that each inducer elicited a unique response from the actinomycetes and that some chemical responses were specific to each inducer-producer combination. Among these 28 metabolites, hydrazidomycin D, a new hydrazide-containing natural product was isolated from the pair sp. RKBH-B178 and . This result validated the effectiveness of the strategy in discovering new natural products. From the same set of induced metabolites, an in-depth investigation of a fermentation of sp. RKBH-B178 and autoclaved led to the discovery of a glucuronidated analog of the pseudomonas quinolone signal (PQS). We demonstrated that RKBH-B178 is able to biotransform the quorum sensing molecules, 2-heptyl-4-quinolone (HHQ), and PQS to form PQS-GlcA. Further, PQS-GlcA was shown to have poor binding affinity to PqsR, the innate receptor of HHQ and PQS.
在此,我们描述了一种改良的细菌培养方法,作为一种通过向放线菌发酵培养基中添加经高压灭菌的“诱导剂”微生物培养物来发现新天然产物的工具。使用七种放线菌和四种诱导剂微生物,我们在基于超高效液相色谱-高分辨电喷雾电离质谱(UHPLC-HRESIMS)的细菌发酵分析中检测到28种被诱导的代谢物。代谢组学分析表明,每种诱导剂都会引发放线菌独特的反应,并且一些化学反应对每种诱导剂-产生菌组合具有特异性。在这28种代谢物中,从菌株RKBH-B178和[未提及的菌株名称]的组合中分离出了一种新的含酰肼天然产物——酰肼霉素D。这一结果验证了该策略在发现新天然产物方面的有效性。从同一组诱导代谢物中,对菌株RKBH-B178和经高压灭菌的[未提及的微生物名称]的发酵进行深入研究,发现了一种假单胞菌喹诺酮信号(PQS)的葡萄糖醛酸化类似物。我们证明RKBH-B178能够将群体感应分子2-庚基-4-喹诺酮(HHQ)和PQS进行生物转化,形成PQS-GlcA。此外,PQS-GlcA被证明与HHQ和PQS的天然受体PqsR的结合亲和力较差。