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食用菌中L-色氨酸HPLC检测方法的建立

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建立了高效液相色谱(high performance liquid chromatography,HPLC)测定食用菌中L-色氨酸含量的方法,并进行了方法学验证.采用AcclaimTM 120 C18 色谱柱(4.6 mm×250 mm,5 μm),以 0.05 moL·L-1 乙酸钠缓冲液(用冰乙酸将pH调至 4.0~5.0)和纯甲醇为流动相(体积比为 70∶30)等度洗脱,流速为 1.0 mL·min-1,检测波长为 280 nm,柱温为 30℃,进样量为 20 μL.结果显示L-色氨酸在 4~100 μg·mL-1 线性关系良好,R2>0.995 5.精密度、重复性、24h内稳定性的相对标准偏差均小于 15%(n=6),加标回收率为 87.5%(相对标准偏差为 0.63%).说明建立的高效液相色谱检测方法简单、快速、灵敏度高、特异性强、分离度好,适用于食用菌中L-色氨酸含量的测定.
Establishment of HPLC Detection Method for L-tryptophan in Edible Fungi
Methodological validation was conducted on the established high performance liquid chromatography(HPLC)method for determining L-tryptophan content in edible fungi.Using an AcclaimTM 120 C18 chromatography column(4.6 mm×250 mm,5 μm),isometric elution was performed with 0.05 mol·L-1 sodium acetate buffer(pH adjusted to 4.0-5.0 with glacial acetic acid)and pure methanol as mobile phases(the volume ratio is 70∶30),with a flow rate of 1.0 mL·min-1,detection wavelength of 280 nm,column temperature of 30℃,and injection volume of 20 μL.The results showed that L-tryptophan showed a good lin-ear relationship in the range of 4-100 μg·mL-1,and the R2>0.995 5.The relative standard deviation of precision,repeatability and stability within 24 hours is less than 15%(n=6),and the spiked recovery rate was 87.5%(relative standard deviation was 0.63%).The established HPLC detection method is simple,fast,highly sensitive,specific,and has good separation,it is suitable for the determination of L-tryptophan content in edible fungi.

edible fungiL-tryptophanhigh performance liquid chromatography

游金坤、孙达锋、代秋琼、曹燕妮、邓雅元、华蓉

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中华全国供销合作总社昆明食用菌研究所,云南 昆明 650221

云南云菌科技(集团)有限公司,云南 昆明 650221

云南省食用菌产业发展研究院,云南 昆明 650221

食用菌 L-色氨酸 高效液相色谱

2024

中国食用菌
中国食用菌协会 中华全国供销合作总社昆明食用菌研究所 全国食用菌科技情报中心站

中国食用菌

影响因子:0.574
ISSN:1003-8310
年,卷(期):2024.43(6)