Lee, H.X. and Ahmad, F. and Saad, B. and Ismail, M.N. (2017) Evaluation of extraction methods for the identification of proteins from date palm (Phoenix dactylifera L.) seed and flesh. Preparative Biochemistry and Biotechnology, 47 (10). pp. 998-1007. ISSN 10826068
Full text not available from this repository.Abstract
Date fruits are well known to be very nutritious. Nevertheless, the protein contents of the fruit, particularly the seed and flesh, are still understudied, largely due to their difficult physical characteristics. This study was conducted to compare three different protein extraction methods which were the trichloroacetic acid (TCA)-acetone (TCA-A), phenol (Phe), and TCA-acetone-phenol (TCA-A-Phe), and to perform proteomic analysis on date palm seed and flesh. Phe extraction method showed the highest protein yields for both seed (8.26 mg/g) and flesh (1.57 mg/g). Through sodium dodecyl sulfate-polyacrylamide gel electrophoresis, Phe, and TCA-A-Phe extraction methods were shown to be efficient in removing interfering compounds and gave well-resolved bands over a wide range of molecular weights. Following liquid chromatography�tandem mass spectrometry analysis, about 50�64 of extracted proteins were identified with known functions including those involved in glycolysis, Krebs cycle, defense, and storage. Phe protein extraction method was proven to be the optimal method for date flesh and seed. © 2017 Taylor & Francis.
Item Type: | Article |
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Additional Information: | cited By 4 |
Uncontrolled Keywords: | acetone; phenol; plant protein; trichloroacetic acid, chemistry; fruit; isolation and purification; Phoenix (plant); plant seed; polyacrylamide gel electrophoresis; procedures; tandem mass spectrometry, Acetone; Electrophoresis, Polyacrylamide Gel; Fruit; Phenol; Phoeniceae; Plant Proteins; Seeds; Tandem Mass Spectrometry; Trichloroacetic Acid |
Depositing User: | Mr Ahmad Suhairi UTP |
Date Deposited: | 09 Nov 2023 16:19 |
Last Modified: | 09 Nov 2023 16:19 |
URI: | https://khub.utp.edu.my/scholars/id/eprint/8127 |