Wu Zhichao, Wu Enguo, Yang Zhongyi, Tao Yuxiang, Chen Tan, Zhong Yongjun
Taizhou University, Taizhou 318000, China.
Zhejiang Hisun Pharmaceutical Co., Ltd., Taizhou 318000, China.
Se Pu. 2019 Oct 8;37(10):1118-1123. doi: 10.3724/SP.J.1123.2019.03033.
A method was developed for the determination of '-ethylenediamine disuccinic acid (EDDS) in bioconversion samples by high performance liquid chromatography (HPLC). An InertSustain AQ-C column (250 mm×4.6 mm, 5 μm) was used in the analysis. The mobile phase was 25% (v/v) methanol with 1.0 g/L Cu(COCH)·HO, 2.0 g/L tetrabutylammonium hydroxide, and the pH was adjusted to 2.80 with phosphoric acid. The flow rate of the mobile phase was 1.0 mL/min, and the column temperature was set at 30℃. The detection wavelength was 254 nm. EDDS, fumaric acid, citric acid, malic acid and ethylenediaminetetraacetic acid (EDTA) were separated from one another within 8 min. EDDS showed good linearity in the range of 0.06-0.6 g/L. About 0.25 g/L EDDS was detected in the biosynthesis reaction solution catalyzed by recombinant EDDS-lyase, while 36.56 g/L malic acid was formed as the by-product from fumaric acid. The catalytic activity of the enzyme was confirmed in the hydrolysis of 10 g/L EDDS, which produced 3.05 g/L malic acid in 3 h. This analytical method is simple, rapid, sensitive, reliable, and suitable for the analysis in the research of EDDS bioconversion process.
建立了一种通过高效液相色谱(HPLC)测定生物转化样品中乙二胺二琥珀酸(EDDS)的方法。分析中使用InertSustain AQ-C柱(250 mm×4.6 mm,5 μm)。流动相为含1.0 g/L Cu(COCH)·HO、2.0 g/L氢氧化四丁铵的25%(v/v)甲醇,并用磷酸将pH调至2.80。流动相流速为1.0 mL/min,柱温设定为30℃,检测波长为254 nm。EDDS、富马酸、柠檬酸、苹果酸和乙二胺四乙酸(EDTA)在8分钟内彼此分离。EDDS在0.06 - 0.6 g/L范围内呈良好线性。在重组EDDS裂解酶催化的生物合成反应溶液中检测到约0.25 g/L的EDDS,同时由富马酸形成36.56 g/L苹果酸作为副产物。该酶在10 g/L EDDS水解反应中表现出催化活性,3小时内产生3.05 g/L苹果酸。该分析方法简单、快速、灵敏、可靠,适用于EDDS生物转化过程研究中的分析。