来自Bifidobacterium bifidum的32个家族碳水化合物结合模块对乳糖-N-生物酶I识别的结构洞察力
Xinzhe Zhang1, Naoki Sunagawa2, Toma Kashima1,3
1Department of Biotechnology, The University of Tokyo, Japan.
FEBS letters
|November 8, 2025
概括
比菲多细菌 (Bifidobacterium bifidum) 通过LnbB酶从人乳寡糖化物 (HMO) 中使用乳酸-N-生物I (LNB). 这项研究揭示了LnbB的CBM32域的结构和功能,解释了它如何结合LNB来支持婴儿肠道微生物组.
科学领域:
- 微生物学 微生物学
- 结构生物学 结构生物学
- 葡萄糖生物学 葡萄糖生物学
背景情况:
- 比菲多细菌 (Bifidobacterium bifidum) 是一个关键的婴儿肠道微生物.
- 它会代谢人乳寡糖 (HMO),包括乳酸-N-生物I (LNB).
- 乳酸-N-生物酶 (LnbB) 在HMO降解过程中对LNB释放至关重要.
研究的目的:
- 研究Bifidobacterium bifidum的LnbB.中的CBM32域的结构和功能.
- 为了阐明LNB由LnbB的CBM32域结合的分子机制.
主要方法:
- 异热定位热量计 (ITC) 来评估LNB结合亲和力.
- 用X射线结晶学测定CBM32与LNB的复杂结构.
主要成果:
- LnbB的CBM32域将LNB与98μm的解离常数 (Kd) 结合在一起.
- 晶体结构揭示了CBM32和LNB之间的特定分子相互作用.
结论:
- 对于Bifidobacterium bifidum来说,CBM32域是必不可少的,它可以从HMO中捕获LNB.
- 这种机制促进了LNB交叉养,促进了其他双菌的生长,并支持了婴儿肠道生态系统.
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