色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
12期
1400-1403
,共4页
徐颖%臧颖%姜婷%郑兆娟%欧阳嘉
徐穎%臧穎%薑婷%鄭兆娟%歐暘嘉
서영%장영%강정%정조연%구양가
高效阴离子交换色谱%海藻糖%葡萄糖%麦芽糖%生物转化样品
高效陰離子交換色譜%海藻糖%葡萄糖%麥芽糖%生物轉化樣品
고효음리자교환색보%해조당%포도당%맥아당%생물전화양품
high performance anion exchange chromatography( HPAEC)%trehalose%glucose%maltose%biotransformation sample
建立了高效阴离子交换色谱-脉冲安培电化学检测法同时测定生物转化样品中海藻糖、葡萄糖和麦芽糖的分析方法。选用 CarboPacTM10色谱柱(250 mm×2 mm)对分离条件进行优化,使用标准样品测定了线性范围和工作曲线,柱温为30℃,流速为0.30 mL/min,以氢氧化钠溶液和醋酸钠溶液为流动相进行梯度洗脱,脉冲安培法进行检测。研究结果表明,该方法可在15 min内实现海藻糖生物转化液中3种糖的快速定量分析。海藻糖、葡萄糖和麦芽糖峰面积与质量浓度的线性关系良好,检出限为0.010~0.100 mg/L。将此方法用于酶法制备海藻糖的检测,加标回收率为89.40%~103.2%。在生物转化样品中检测到海藻糖浓度为101.084 g/L,转化率达到了50.5%。该方法灵敏度高,简便快速,可应用于海藻糖制备样品中各种成分的分离和定量检测。
建立瞭高效陰離子交換色譜-脈遲安培電化學檢測法同時測定生物轉化樣品中海藻糖、葡萄糖和麥芽糖的分析方法。選用 CarboPacTM10色譜柱(250 mm×2 mm)對分離條件進行優化,使用標準樣品測定瞭線性範圍和工作麯線,柱溫為30℃,流速為0.30 mL/min,以氫氧化鈉溶液和醋痠鈉溶液為流動相進行梯度洗脫,脈遲安培法進行檢測。研究結果錶明,該方法可在15 min內實現海藻糖生物轉化液中3種糖的快速定量分析。海藻糖、葡萄糖和麥芽糖峰麵積與質量濃度的線性關繫良好,檢齣限為0.010~0.100 mg/L。將此方法用于酶法製備海藻糖的檢測,加標迴收率為89.40%~103.2%。在生物轉化樣品中檢測到海藻糖濃度為101.084 g/L,轉化率達到瞭50.5%。該方法靈敏度高,簡便快速,可應用于海藻糖製備樣品中各種成分的分離和定量檢測。
건립료고효음리자교환색보-맥충안배전화학검측법동시측정생물전화양품중해조당、포도당화맥아당적분석방법。선용 CarboPacTM10색보주(250 mm×2 mm)대분리조건진행우화,사용표준양품측정료선성범위화공작곡선,주온위30℃,류속위0.30 mL/min,이경양화납용액화작산납용액위류동상진행제도세탈,맥충안배법진행검측。연구결과표명,해방법가재15 min내실현해조당생물전화액중3충당적쾌속정량분석。해조당、포도당화맥아당봉면적여질량농도적선성관계량호,검출한위0.010~0.100 mg/L。장차방법용우매법제비해조당적검측,가표회수솔위89.40%~103.2%。재생물전화양품중검측도해조당농도위101.084 g/L,전화솔체도료50.5%。해방법령민도고,간편쾌속,가응용우해조당제비양품중각충성분적분리화정량검측。
An analytical method for the determination of trehalose,maltose,and glucose in biotransformation samples was developed by using high performance anion exchange chroma-tography coupled with pulsed ampere detection( HPAEC-PAD). The analysis was performed on a CarboPacTM 10 column( 250 mm × 2 mm ) with the gradient elution of NaOH-NaAc as the mobile phase. The column temperature was set at 30 ℃,the flow rate was 0. 30 mL/min. The results showed that trehalose,maltose,and glucose in biotransformation system were com-pletely separated and determined in 15 min. The linear ranges and the working curves were determined by using standard samples. The correlation coefficients of three kinds of carbohy-drates were over 0. 999 8 . The detection limits( LODs)were 0. 010-0. 100 mg/L. Under the optimized separation conditions,the recoveries of saccharides in the transformation system at three different spiked levels ranged from 89. 4% to 103. 2%. In biotransformation system,50 IU trehalose synthase were added into 200 g/L maltose for reaction of 8 h at 37 ℃,pH 8. 0. Under the above conditions,the concentration of trehalose in biotransformation sample was 101. 084 g/L,and the conversion rate of trehalose reached 50. 5%. The method can be applied to deter-mine the composition in the transformation system with the advantages of simplicity and con-venience.