| Literature DB >> 31642292 |
Zhichao Wu1, Enguo Wu2, Zhongyi Yang1, Yuxiang Tao3, Tan Chen1, Yongjun Zhong1.
Abstract
A method was developed for the determination of N,N'-ethylenediamine disuccinic acid (EDDS) in bioconversion samples by high performance liquid chromatography (HPLC). An InertSustain AQ-C18 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(CO2CH3)2·H2O, 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.Entities:
Keywords: N,N'-ethylenediamine disuccinic acid (EDDS); bioconversion; chelating agent; high performance liquid chromatography (HPLC); reversed-phase ion pair chromatography
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Year: 2019 PMID: 31642292 DOI: 10.3724/SP.J.1123.2019.03033
Source DB: PubMed Journal: Se Pu ISSN: 1000-8713