Ghosh Bidisha, Mitra Joy, Chakraborty Saikat, Bhattacharyya Jagannath, Chakraborty Anirban, Sen Soumitra Kumar, Neerathilingam Muniasamy
Protein Technology Core, Centre for Cellular and Molecular Platforms, NCBS-TIFR, Bangalore, Karnataka, India.
Advanced Laboratory for Plant Genetic Engineering, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India.
PLoS One. 2015 Nov 2;10(11):e0140649. doi: 10.1371/journal.pone.0140649. eCollection 2015.
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 β-N-oxalyl-L-α,β-diaminopropionic acid (β-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 β-ODAP content in various Lathyrus plants. Currently available HPLC based methods involve multi-step derivatization of the sample. To overcome this, we have developed β-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 β-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.
草豌豆是印度北部大部分地区和非洲干旱及饥荒易受灾地区廉价且营养丰富的食物来源。非蛋白质氨基酸β-N-草酰-L-α,β-二氨基丙酸(β-ODAP)数十年来一直因其强大的神经毒性作用而为人所知,它会导致不可逆的神经退行性疾病“骨痛病”,草豌豆及其他物种的种子和叶子中均不同程度地含有这种物质。建立一种快速且可靠的方法来检测各种草豌豆植物中β-ODAP的含量至关重要。目前基于高效液相色谱法(HPLC)的方法需要对样品进行多步衍生化。为克服这一问题,我们开发了一种无需任何预先衍生化的HPLC法来分析β-ODAP。该方法在2至100μg/ml范围内具有统计学意义,呈现出线性响应,r2>0.99。该方法的检测限和定量限分别确定为5.56μg/ml和16.86μg/ml。除此之外,还开发了一种基于薄层色谱法(TLC)的方法。β-ODAP的检测限为0.6μg,其底物L-1,2-二氨基丙酸的检测限为5μg。通过进行体外生物转化试验以检测植物提取物中生物催化剂的存在,对HPLC和TLC方法均进行了验证。该方法经济、快速且简便。