在真核生物中,从D-葡萄糖到D-阿拉比诺酸的路径被提出
Elda Iljazi1, Rupa Nagar1, Sabine Kuettel1
1Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee, Scotland, UK.
The Journal of biological chemistry
|June 29, 2024
概括
研究人员发现了一条新的真核细胞途径,用于从D-葡萄糖 (D-Glc) 中生物合成D-阿拉比诺斯 (D-Ara). 这项研究涉及酸路径,并确定谷氨酸果糖-6-酸胺转移酶 (GFAT) 作为D-Ara生产中的关键酶.
科学领域:
- 生物化学和分子生物学
- 代谢途径 代谢途径
- 单核细胞生物学 单核细胞生物学
背景情况:
- D-arabinose (D-Ara) 是真核生物合成中的一个关键中间体,包括D-erythroascorbate和GDP-α-D-arabinopyranose (GDP-D-Arap).
- 在真核生物中,从D-葡萄糖 (D-Glc) 获得D-Ara的生物合成途径在很大程度上仍未表征,与 prokaryotes 不同.
研究的目的:
- 为了阐明未知的真核细胞途径,从D-Glc.中进行D-Ara生物合成.
- 为了确定涉及到这个转化中的特异性酶和中间体,在tripanosomatid *Crithidia fasciculata*.
主要方法:
- 作为前体,使用位置标记为[13C]-D-Glc和[13C]-D-ribose ([13C]-D-Rib).
- 采用了一种新的衍生和气色谱-质谱法 (GC-MS) 程序,对利波阿拉比诺.
- 测试了*C. fasciculata*假定的糖和聚醇酸盐异构酶基因,以补充一个*Escherichia coli* D-Ara-5P异构酶缺乏突变体.
主要成果:
- 数据表明酸途径的参与和D-ribulose-5-phosphate (D-Ru-5P) 到D-Ara-5P的同质化.
- 从*C. fasciculata*中获得的葡萄糖胺-6-酸盐氨基转移酶 (GFAT) 拯救了*大肠杆菌*的突变.
- 来自其他真核生物 (trypanosomatids,酵母,人类) 的GFAT基因也补充了*大肠杆菌*突变,人类的GFAT生物化学异构D-Ru-5P到D-Ara5P.
结论:
- 建议从D-Glc中进行D-Ara生物合成的通用真核细胞途径,涉及GFAT.
- 在 *C. fasciculata* 中的 D-Ara 可能用于 GDP-D-Arap,表面糖联合物和 D-erythroascorbate 合成.
- 已确定的GFAT介导途径为各种真核生物体的糖代谢提供了洞察力.
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