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An integrated approach for phytate degradation and recovery of myo-inositol and phosphate as value-added products from the by-products of corn ethanol industry.

机译:肌醇分解和回收肌醇和磷酸盐作为玉米乙醇工业副产品的增值产品的综合方法。

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摘要

An integrated process was developed to hydrolyze the phytates in light steep water (LSW) and to simultaneously isolate inorganic phosphate (Pi) and myo-inositol products. The proposed integrated process is helpful in resolving the environmental and nutritional concerns in the use of corn gluten feed (CGF) in the animal diets. This process comprised of partial and total hydrolysis of LSW and intermediate anion exchange separation technique. The phytates in LSW were initially degraded to negatively charged myo-inositol phosphates (InsP2 -- InsP5). The optimized experimental parameters for the partial hydrolysis of LSW were determined to be 2 h hydrolysis with 1 FTU A. niger/g substrate at 35°C. The negatively charged species of the partially hydrolyzed substrate were separated on a strong base anion exchange resin. The negatively charged species, retained by the resin, were eluted with 1M NaCl solution and were subjected to complete hydrolysis with E. coli, A. niger-derived phytases and their respective combinations. The maximum amount of myo-inositol released from the anion exchange column was detected after 48 h reactions catalyzed by 100 FTU E. coli , 150 FTU E. coli, and 150 FTU the combination of A. niger and E. coli. The time course of Pi released showed a similar trend to that of myo-inositol and the released Pi reached a maximum amount after 48 h incubation at the enzyme loadings for which the maximum concentration of myo-inositol were reached.;An isocratic HPLC method was developed for routine analysis of myo-inositol and Pi. For myo-inositol, the limit of detection (LOD) was 0.01 mg/ml, and the limit of quantification (LOQ) was 0.04 mg/ml. The linear range of this method for myo-inositol was 0--20 mg/ml. The HPLC method is also a fast method for Pi quantification in the hydrolysate. The linear range of this method for Pi was 0--10 mg/ml. The LOD and LOQ were 0.05 and 0.17 mg/ml, respectively.;A size-exclusion chromatography packed was developed for isolating and purifying myo-inositol and Pi, from the mixture with E. coli phytase and Cl-.
机译:开发了一种集成方法来在轻水(LSW)中水解肌醇六磷酸,同时分离出无机磷酸盐(Pi)和肌醇产品。拟议的综合方法有助于解决动物日粮中使用玉米蛋白饲料(CGF)的环境和营养问题。该过程包括LSW的部分和全部水解以及中间阴离子交换分离技术。 LSW中的肌醇六磷酸最初被降解为带负电荷的肌醇磷酸酯(InsP2-InsP5)。确定LSW部分水解的最佳实验参数为在35°C下用1 FTU黑曲霉/ g底物进行2 h水解。在强碱阴离子交换树脂上分离部分水解的底物带负电荷的物质。用1M NaCl溶液洗脱被树脂保留的带负电荷的物质,并用大肠杆菌,黑曲霉衍生的植酸酶及其各自的组合进行完全水解。在100 FTU大肠杆菌,150 FTU大肠杆菌和150 FTU黑曲霉和大肠杆菌的组合催化下反应48小时后,检测到从阴离子交换柱释放的肌醇的最大量。 Pi释放的时间进程显示出与肌醇相似的趋势,并且在达到最大肌醇浓度的酶负荷下孵育48 h后,Pi释放达到最大量。开发用于肌醇和Pi的常规分析。对于肌醇,检测限(LOD)为0.01 mg / ml,定量限(LOQ)为0.04 mg / ml。该方法对肌醇的线性范围是0--20mg / ml。 HPLC方法也是水解产物中Pi定量的快速方法。该方法对Pi的线性范围是0--10 mg / ml。 LOD和LOQ分别为0.05和0.17 mg / ml。开发了一种体积排阻色谱法,用于从大肠杆菌肌醇六磷酸酶和Cl-的混合物中分离和纯化肌醇和Pi。

著录项

  • 作者

    Dang, Jun.;

  • 作者单位

    The University of Nebraska - Lincoln.;

  • 授予单位 The University of Nebraska - Lincoln.;
  • 学科 Engineering Agricultural.;Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 166 p.
  • 总页数 166
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:44:24

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