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Production medium optimization and structural characterization of an extracellular polysaccharide produced by

机译:生产中等优化和生产细胞外多糖的结构表征

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摘要

Several strains of microorganism are capable of converting carbohydrates into extracellular polysaccharide. The preset research is a first effort made to optimize extracellular polysaccharide (CRMEP) by Rhodotorula minuta ATCC 10658 using one factor at time and response surface methods. One factor at time was applied in the initial screening of substrates prior to optimization study. Of all the substrates examined, starch as carbon source and defatted soy bean powder as protein source were discovered to be best for CRMEP production. Response surface analysis revealed that 15 g/L starch and 30g/L defatted soy bean powder were the optimal chemical conditions. The model predicted 13.22 g/L for CRMEP, which went along with the experimentally observed result. Purification of CRMEP by anion‐exchange column of DEAE‐cellulose yielded RMEP. Structural investigation indicated that the main chain of RMEP was composed of (1 → 3) and (1 → 4)‐linked mannopyranosyl residues, with branches attached to O‐6 of some (1 → 3)‐linked mannopyranosyl residues. The branches were composed of Glcp‐(1 → residues.
机译:几种微生物菌株能够将碳水化合物转化为细胞外多糖。预设的研究是使用rhodotorula Minuta ATCC 10658在时间和响应表面方法中优化rhodotorula minuta ATCC 10658的第一次努力。在优化研究之前,在初始筛选中应用了一个因素。在检查的所有基材中,发现淀粉作为碳源和脱脂大豆粉作为蛋白质来源是最适合CRMEP生产的。响应表面分析显示,15g / l淀粉和30g / L脱脂大豆粉是最佳的化学条件。对于CRMEP预测的模型,与实验观察结果一起进行了13.22克/ L.通过DEAE-纤维素的阴离子交换柱纯化CRMEP产生RMEP。结构调查表明,RMEP的主链由(1→3)和(1→4) - 链接的甘露糖基残基组成,其中分支与一些(1→3) - 链接甘露糖基残基的O-6附着。分支由GLCP-(1→残留物组成。

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