Graduate School of Science and Engineering, Kagoshima University, 1-21-40 Korimoto, Kagoshima 890-0065, Japan.
Graduate School of Science and Engineering, Kagoshima University, 1-21-40 Korimoto, Kagoshima 890-0065, Japan.
Carbohydr Polym. 2016 Oct 20;151:1034-1039. doi: 10.1016/j.carbpol.2016.06.057. Epub 2016 Jun 16.
α-Glucan phosphorylase catalyzes enzymatic polymerization of α-d-glucose 1-phosphate (Glc-1-P) as a monomer from a maltooligosaccharide primer to produce α(1→4)-glucan, i.e., amylose, with liberating inorganic phosphate (Pi). Because of quite weak specificity for the recognition of substrates by thermostable α-glucan phosphorylase (from Aquifex aeolicus VF5), in this study, we investigated the enzymatic copolymerization of Glc-1-P with its analogue monomer, α-d-mannose 1-phosphate (Man-1-P) under the conditions for removal of Pi as the precipitate with ammonium and magnesium in ammonia buffer containing Mg(2+) ion to produce α(1→4)-linked non-natural mannoglucans composed of Glc/Man units. The reaction was conducted in different feed ratios using the maltotriose primer at 40°C for 7days. The MALDI-TOF mass and (1)H NMR spectra of the products fully supported the mannoglucan structures.
α-葡聚糖磷酸化酶催化从麦芽寡糖引物上将α-d-葡萄糖 1-磷酸(Glc-1-P)作为单体进行酶聚合反应,生成α(1→4)-葡聚糖,即直链淀粉,并释放无机磷酸(Pi)。由于热稳定α-葡聚糖磷酸化酶(来自 Aquifex aeolicus VF5)对底物的识别特异性相当弱,因此在本研究中,我们在氨缓冲液中含有 Mg(2+)离子的情况下,使用铵盐和镁将 Pi 作为沉淀物去除,以研究 Glc-1-P 与类似的单体α-d-甘露糖 1-磷酸(Man-1-P)的酶共聚合反应,以生产由 Glc/Man 单元组成的α(1→4)-连接的非天然甘露葡聚糖。使用麦芽三糖作为引物,在 40°C 下进行不同进料比的反应,持续 7 天。产物的 MALDI-TOF 质量和 (1)H NMR 谱完全支持甘露聚糖结构。