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机构地区:[1]南京工业大学制药与生命科学学院,南京210009
出 处:《分析化学》2007年第11期1651-1653,共3页Chinese Journal of Analytical Chemistry
基 金:国家863计划(No2006AA03Z0453);973计划(No2007CB714304)资助项目
摘 要:对于生物法制备丙酸的微生物发酵体系,利用Waters Atlantis dC18反相色谱柱,以0.01mol/LKH2PO4缓冲液(pH2.8)-乙腈(95:5,V/V)作流动相,在流速为1.0mL/min,柱温为25℃时,于紫外波长215nm处检测,9min内发酵液中的草酸、甲酸、乙酸、乳酸、琥珀酸和丙酸能得到良好分离。6种有机酸线性相关系数均在0.9992-1.0000之间;方法的回收率为99%~102%;RSD为0.56~1.66。本方法能够简便、快速测定丙酸发酵体系中主产物丙酸与其它有机酸含量,适于指导整个发酵过程条件的优化及发酵产物的监控。Water altanlis with dC18 column and mobile phase contained 10 mmol/L potassium dihydrogen phosphate buffer (pH 2.8) and acetonitrile (95:5, V/V) was used to determin organic acid in propioic acid fermenlation system. The flow rate was 1.00 mL/min and the column temperature was 25℃. Oxalic acid, formic acid, lactic acid, acetic acid, succinic acid and propionic acid were completely separated and determined with UV detector at 215 nm in 9 min. All the correlation coefficients(r) were between 0.9992 and 1. 0000, and the recovery ranged from 99% to 102%. The relative standard deviation was in the range of 0.6% - 1.7%. By this method, propionic acid and other organic acids could be rapidly and effectively determined.
分 类 号:TQ920[轻工技术与工程—发酵工程]
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