Bulet P, Hoflack B, Porchet M, Verbert A
Eur J Biochem. 1984 Oct 15;144(2):255-9. doi: 10.1111/j.1432-1033.1984.tb08458.x.
Homogenates of Perinereis cultrifera oocytes were found to transform GDP-D-mannose into another sugar nucleotide. Ultraviolet absorption spectra, chromatographic behaviour, gas-liquid chromatography coupled to mass spectrometry analysis revealed that GDP-D-mannose had been converted into GDP-L-fucose. This conversion is a multi-step reaction as proved by the involvement of two intermediates identified as GDP-4-oxo-6-deoxy-D-mannose and GDP-4-oxo-6-deoxy-L-galactose, this latter being reduced by NADPH to give GDP-L-fucose. It is shown that the enzymatic activities responsible for the conversion of GDP-D-mannose into GDP-L-fucose is recovered only in oocytes and is not present in the other coelomic cells (i.e. coelomocytes). More interesting is the fact that maximum activity is recovered at a well defined stage of the hormone-controlled oogenesis. Thus, this enzymatic system appears as a biochemical marker of the oocyte maturation in P. cultrifera.
研究发现,沙蚕(Perinereis cultrifera)卵母细胞的匀浆能够将GDP-D-甘露糖转化为另一种糖核苷酸。紫外吸收光谱、色谱行为以及气相色谱-质谱联用分析表明,GDP-D-甘露糖已被转化为GDP-L-岩藻糖。这种转化是一个多步反应,这一点已通过鉴定出的两种中间体得到证明,这两种中间体分别为GDP-4-氧代-6-脱氧-D-甘露糖和GDP-4-氧代-6-脱氧-L-半乳糖,后者被NADPH还原生成GDP-L-岩藻糖。结果表明,负责将GDP-D-甘露糖转化为GDP-L-岩藻糖的酶活性仅在卵母细胞中检测到,而在其他体腔细胞(即体腔细胞)中不存在。更有趣的是,在激素控制的卵子发生的一个明确阶段,该酶活性达到最大值。因此,这个酶系统似乎是沙蚕卵母细胞成熟的一个生化标志物。