Applications of the ninhydrin reaction for analysis of amino acids, peptides, and proteins to agricultural and biomedical sciences

被引:482
作者
Friedman, M [1 ]
机构
[1] USDA ARS, Western Reg Res Ctr, Albany, CA 94710 USA
关键词
ninhydrin; Ruhemann's purple; amino acids; peptides; proteins; analysis; food chemistry; protein chemistry; clinical chemistry; histochemistry; fo; rensic science; microbiology; medicine; nutrition; pharmacology; plant science; toxicology; proteolysis; cereal proteins; keratin proteins; milk proteins; soy proteins; whey proteins; protein-tannin complexes; cheeses; fruits; vegetables;
D O I
10.1021/jf030490p
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The reaction of ninhydrin with primary amino groups to form the purple dye now called Ruhemann's purple (RIP) was discovered by Siegfried Ruhemann in 1910. In addition, imines such as pipecolic acid and proline, the guanidino group of arginine, the amide groups of asparagine, the indole ring of tryptophan, the sulfhydryl group of cysteine, amino groups of cytosine and guanine, and cyanide ions also react with ninhydrin to form various chromophores of analytical interest. Since its discovery, extensive efforts have been made to apply manual and automated ninhydrin reactions as well as ninhydrin spray reagents to the detection, isolation, and analysis of numerous compounds of interest across a broad spectrum of disciplines. These include agricultural, biochemical, clinical, environmental, food, forensic, histochemical, microbiological, medical, nutritional, plant, and protein sciences. This reaction is unique among chromogenic reactions in that at pH 5.5 it results in the formation of the same soluble chromophore by all primary amines which react, be they amines, amino acids, peptides, proteins, and even ammonia. Because the chromophore is not chemically bound to the protein or other insoluble material, it is not lost when the insoluble substrate is removed by centrifugation or filtration after the reaction is completed. The visible color of the chromophore is distinctive and is generally not affected by the yellow colors present in many food, plant, and tissue extracts. Adaptations of the classical ninhydrin reaction to specialized needs; in analytical chemistry and biochemistry include the use of acid, alkaline, and fluorogenic ninhydrin reagents. To cross-fertilize information among several disciplines wherein an interest in the ninhydrin reaction has developed, and to enhance its utility, this review attempts to integrate and correlate the widely scattered literature on ninhydrin reactions of a variety of structurally different compounds. Specifically covered are the following aspects: historical perspective, chemistry and mechanisms, applications, and research needs. A better understanding of these multifaceted ninhydrin, reactions provide a scientific basis for further improvements of this important analytical technique.
引用
收藏
页码:385 / 406
页数:22
相关论文
共 261 条
[1]   Colorimetric determination of gabapentin in pharmaceutical formulation [J].
Abdellatef, HE ;
Khalil, HM .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2003, 31 (01) :209-214
[2]  
ABDERHALDEN E, 1911, Z PHYSL CHEM, V72, P37
[3]  
ABDERHALDEN E, 1913, Z PHYSL CH, V85, P143
[4]  
AHOKAS H, 1989, CEREAL CHEM, V66, P135
[5]   Effect of ninhydrin on the biochemical and histopathological changes induced by ethanol in gastric mucose of rats [J].
Al-Shabanah, OA ;
Raza, M ;
Al-Harbi, MM ;
Al-Bekairi, AM ;
Al-Gharably, NM ;
Qureshi, S .
LIFE SCIENCES, 2000, 67 (05) :559-566
[6]   DIRECT ESTIMATION OF LYSINE IN CORN MEALS BY NINHYDRIN COLOR-REACTION [J].
BECKWITH, AC ;
PAULIS, JW ;
WALL, JS .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1975, 23 (02) :194-196
[7]   Nonprotein amino acids of plants: Significance in medicine, nutrition, and agriculture [J].
Bell, EA .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (10) :2854-2865
[9]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF AN ARGININE-CONTAINING OCTAPEPTIDE ANTAGONIST OF VASOPRESSIN IN HUMAN PLASMA BY MEANS OF A SELECTIVE POSTCOLUMN REACTION WITH FLUORESCENCE DETECTION [J].
BOPPANA, VK ;
RHODES, GR .
JOURNAL OF CHROMATOGRAPHY, 1990, 507 :79-84
[10]   Lysinoalanine content of formulas for enteral nutrition [J].
Boschin, G ;
D'Agostina, A ;
Rinaldi, A ;
Arnoldi, A .
JOURNAL OF DAIRY SCIENCE, 2003, 86 (07) :2283-2287