Lee Thomas Chun-Hung, Lam Winnie, Tam Nora Fung-Yee, Xu Steven Jing-Liang, Lee Chak-Lam, Lee Fred Wang-Fat
School of Science and Technology, Hong Kong Metropolitan University, Hong Kong.
School of Science and Technology, Hong Kong Metropolitan University, Hong Kong; State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong.
Mar Pollut Bull. 2024 Dec;209(Pt B):117227. doi: 10.1016/j.marpolbul.2024.117227. Epub 2024 Nov 4.
Omics technology has been employed in recent research on algicidal bacteria, but previous transcriptomic studies mainly focused on bacteria or algae, neglecting their interaction. This study explores interactions between algicidal bacterium Maribacter dokdonesis P4 and target alga Karenia mikimotoi KMHK using proteomics. Proteomics responses of KMHK after co-culture with P4 in separate compartments of the transwell for 8 and 24 h were evaluated using tandem mass tags (TMT) proteomics, and changes of P4 proteomics were also assessed. Results indicated that essential metabolic processes of KMHK were disrupted after 8 h co-culture with P4. Disturbance of oxidative phosphorylation in mitochondria and electron transport chain in chloroplast raised oxidative stress, leading to endoplasmic reticulum stress and cytoskeleton collapse, and eventual death of KMHK cells. Iron complex outer-membrane receptor protein in P4 was upregulated after co-culture with KMHK for 24 h, suggesting P4 might secrete ferric siderophores, a potential algicidal substance.
组学技术已应用于最近对杀藻细菌的研究中,但以往的转录组学研究主要集中在细菌或藻类上,而忽略了它们之间的相互作用。本研究使用蛋白质组学方法探索杀藻细菌多哥海杆菌P4(Maribacter dokdonesis P4)与目标藻类米氏凯伦藻KMHK(Karenia mikimotoi KMHK)之间的相互作用。使用串联质谱标签(TMT)蛋白质组学评估了KMHK与P4在Transwell独立隔室中共培养8小时和24小时后的蛋白质组学反应,并评估了P4蛋白质组学的变化。结果表明,KMHK与P4共培养8小时后,其基本代谢过程受到破坏。线粒体氧化磷酸化和叶绿体电子传递链的紊乱引发了氧化应激,导致内质网应激和细胞骨架崩溃,最终导致KMHK细胞死亡。P4与KMHK共培养24小时后,其铁复合外膜受体蛋白上调,表明P4可能分泌铁载体,这是一种潜在的杀藻物质。