汉氏葡糖醋杆菌HDM1-3细菌纤维素合成的代谢组学研究OA
Metabolomics Study on Bacterial Cellulose Biosynthesis in Komagataeibacter hansenii HDM1-3
为探究汉氏葡糖醋杆菌(Komagataeibacter hansenii,K.hansenii)HDM1-3 由菌体生长阶段向细菌纤维素(Bacterial cellulose,BC)合成阶段的代谢转变机理,对发酵前期(18 h)和发酵后期(36 h)的K.hansenii HDM1-3 菌株进行非靶向代谢组学分析.对代谢物进行代谢差异筛选,共发现211个差异代谢物.与发酵18 h相比,发酵36 h上调了92 个代谢物,下调了119个代谢物.通路富集分析表明这些代谢物主要富集到淀粉与蔗糖代谢、半乳糖代谢、甘油磷脂代谢、氨基糖与核苷酸糖代谢和鞘脂代谢5条重要代谢通路上.通过KEGG数据库对差异代谢物进一步筛选发现,UDP-葡萄糖、ADP-葡萄糖、蜜二糖和二氢鞘氨醇丰度在发酵18 h和发酵36 h时存在明显差异,可以作为不同发酵时期的潜在生物标志物.总之,本研究分析了K.hansenii HDM1-3生物合成BC前后代谢差异,提出了该菌株在代谢水平上对酸胁迫的潜在响应策略,为阐明K.hansenii HDM1-3 从生长阶段转向纤维素合成的代谢调控机制提供了关键数据,并为后续定向优化细菌纤维素生产提供了潜在的代谢干预靶点.
To investigate the metabolic shift mechanism of Komagataeibacter hansenii(K.hansenii)HDM1-3 from the bacterial growth phase to the bacterial cellulose(BC)synthesis phase,untargeted metabolomics analysis was performed on K.hansenii HDM1-3 cultures at the early fermentation stage(18 h)and late fermentation stage(36 h).Metabolite differential screening identified 211 differential metabolites,with 92 metabolites upregulated and 119 metabolites downregulated at 36 h compared to 18 h.Pathway enrichment analysis indicated that these metabolites were mainly associated with five key metabolic pathways:starch and sucrose metabolism,galactose metabolism,glycerophospholipid metabolism,amino sugar and nucleotide sugar metabolism,and sphingolipid metabolism.Further screening of differential metabolites using the KEGG database showed that UDP-glucose,ADP-glucose,melibiose,and sphinganine exhibited significant abundance differences between 18 h and 36 h of fermentation,suggesting their potential as biomarkers for different fermentation stages.In summary,this study analyzed the metabolic differences in K.hansenii HDM1-3 before and after BC biosynthesis,proposed a potential response strategy of this strain to acid stress at the metabolic level,provided key data for elucidating the metabolic regulatory mechanism underlying the transition from the growth phase to cellulose synthesis in K.hansenii HDM1-3,and identified potential metabolic intervention targets for the subsequent targeted optimization of BC production.
杨承;江柱良;陈俊铭;雷虹;李元敬
华南师范大学 材料与新能源学院,广东 汕尾 516600华南师范大学 材料与新能源学院,广东 汕尾 516600华南师范大学 材料与新能源学院,广东 汕尾 516600黑龙江大学 生命科学院,黑龙江 哈尔滨 150080华南师范大学 材料与新能源学院,广东 汕尾 516600||华南师范大学 行知书院,广东 汕尾 516600
生物科学
汉氏葡糖醋杆菌HDM1-3细菌纤维素非靶向代谢组学差异代谢物
Komagataeibacter hansenii HDM1-3bacterial celluloseuntargeted metabolomicsdifferential metabolites
《纤维素科学与技术》 2026 (1)
8-15,8
国家级大学生创新创业训练计划项目(202310574002)
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