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Simple Detection Methods for Antinutritive Factor ß-ODAP Present in Lathyrus sativus L. by High Pressure Liquid Chromatography and Thin Layer Chromatography.
Ghosh, Bidisha; Mitra, Joy; Chakraborty, Saikat; Bhattacharyya, Jagannath; Chakraborty, Anirban; Sen, Soumitra Kumar; Neerathilingam, Muniasamy.
Affiliation
  • Ghosh B; Protein Technology Core, Centre for Cellular and Molecular Platforms, NCBS-TIFR, Bangalore, Karnataka, India.
  • Mitra J; Advanced Laboratory for Plant Genetic Engineering, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India.
  • Chakraborty S; Advanced Laboratory for Plant Genetic Engineering, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India.
  • Bhattacharyya J; Advanced Laboratory for Plant Genetic Engineering, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India.
  • Chakraborty A; Advanced Laboratory for Plant Genetic Engineering, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India.
  • Sen SK; Advanced Laboratory for Plant Genetic Engineering, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India.
  • Neerathilingam M; Protein Technology Core, Centre for Cellular and Molecular Platforms, NCBS-TIFR, Bangalore, Karnataka, India.
PLoS One ; 10(11): e0140649, 2015.
Article in En | MEDLINE | ID: mdl-26524073
Lathyrus sativus L. (Grass pea) is the source for cheap and nutritious food choice in drought and famine susceptible zones in greater part of North India and Africa. The non-protein amino acid ß-N-oxalyl-L-α,ß-diaminopropionic acid (ß-ODAP) has been known for decades for its potent neurotoxic effect, causing irreversible neurodegenerative disease "neurolathyrism", present in both seed and leaf of Lathyrus sativus L. and other species in varying proportions. It is crucial to establish a rapid as well as reliable detection methodology for ß-ODAP content in various Lathyrus plants. Currently available HPLC based methods involve multi-step derivatization of the sample. To overcome this, we have developed ß-ODAP analysis method by HPLC without any prior derivatization. This method is statistically significant in the range of 2 to 100µg/ml and exhibited linear response with r2 > 0.99. Limit of detection and quantitation of the later method was determined to be 5.56 µg/ml and 16.86 µg/ml, respectively. In addition to this, a TLC based method has also been developed. The limit of detection of ß-ODAP is 0.6µg and for its substrate, L-1,2-diaminopropionic acid is 5µg. Both HPLC and TLC methods were validated by conducting in-vitro bioconversion test to detect the presence of biocatalyst in plant extract. This method is economical, rapid and simple.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, High Pressure Liquid / Chromatography, Thin Layer / Lathyrus / Amino Acids, Diamino Type of study: Diagnostic_studies Country/Region as subject: Africa / Asia Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2015 Document type: Article Affiliation country: India Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, High Pressure Liquid / Chromatography, Thin Layer / Lathyrus / Amino Acids, Diamino Type of study: Diagnostic_studies Country/Region as subject: Africa / Asia Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2015 Document type: Article Affiliation country: India Country of publication: United States