Evaluation of pectinesterase enzyme extracted from Date Palm fruits cv. Zaghloul

Paper Details

Research Paper 01/08/2018
Views (348) Download (16)
current_issue_feature_image
publication_file

Evaluation of pectinesterase enzyme extracted from Date Palm fruits cv. Zaghloul

Ghada A. Ali
Int. J. Biosci.13( 2), 10-17, August 2018.
Certificate: IJB 2018 [Generate Certificate]

Abstract

The idea of this research is to maximize benefits of ripe date palm fruits (cv. Zaghloul) by using it as a source of pectin esterase which is of prime importance for food industry. Pectin esterase was extracted using sodium chloride and its specific activity was determined. The crude pectin esterase specific activity was17849.52Umg-1 protein. Partial purification of the crude enzyme took place with acetone and ethanol to determine the enzyme optimum temperature and pH. The used purification technique resulted in about2.5-fold purification with 20% acetone resulting in 4127.70Umg-1 protein specific activity and16.64% recovery. The same purification fold was obtained with ethanol resulting in4135.44 Umg-1 protein specific activity and 5% recovery. The optimum temperature was 40°C and optimum pH was 8 for the partially purified enzyme. It can be concluded that the quality of pectiesterase enzyme extracted from ripe Zaghloul dates is comparable with that extracted from apple and orange and has specific activity less than apple (30848.90 Umg-1 protein) and more than orange (12736.00 Umg-1 protein).

VIEWS 15

Abdelbasset El Hadrami, Jameel M, Al-Khayri 2012. Socioeconomic and traditional importance of date palm. Emirates Journal for Food and Agriculture 24(5), 371-385.

Alok Kumar Tiwari, Samarendra Nath Saha, Vishnu Prasad Yadav, Uttam Kumar Upadhyay, Deepshikha Katiyar, Tanya Mishra 2017. Extraction and Characterization of Pectin from Orange Peels. International Journal of Biotechnology and Biochemistry 13(1), 39-47.

Bradford, Marion M. 1972. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical biochemistry 72, 248-254.

Dhembare AJ, Kakad SL, Rajani Rana. 2015. Effect of pH, temperature and kinetics of pectinase enzyme using Aspergillus niger by solid-state of fermentation. Journal for Pharmaceutical Sciences 6(8), 1-5.

Duvetter T, Sila DN, Van Buggenhout S, Jolie R, Van Loey A, Hendrickx M.  2009. Pectins in processed fruit and vegetables: Part I—Stability and catalytic activity of pectinases. Institute of Food Technologists, Comprehensive Reviews in Food Science and Food Safety 8, 75-85.

Hagerman AE, Austin PJ. 1986. Continuous spectrophotometric assay for plant pectin methyl esterase. Journal of Agricultural and Food Chemistry 34, 440-444.

IBM Corp. Released. 2014. IBM SPSS Statistics for Windows, Version 23.0. Armonk, NY: IBM Corp.

Julio MontañezSáenz, Alejandro Téllez, Heliodoro de la Garza, María de la Luz Reyes, Juan Carlos Contreras-Esquivel, Cristóbal Noé Aguilar 2000. Purification and some properties of pectinesterase from potato (Solanum tuberosum L.) Alpha Cultivar. Brazilian Archives of Biology and Technology 43(4).

Körner B, Zimmerman G, Berk Z. 1980. Orange pectinesterase: purification, properties, and effect on cloud stability. Journal of Food Science 45, 1203-1206.

Munir N, Asad MJ, Haidri SH. 2015. Production, purification and characterization of Endopolygalacturonase by Bacillus subtillus. Biochemistry and Analytical Biochemistry 4(3), 181.

Shiv Kumar. 2015. Role of enzymes in fruit juice processing and its quality enhancement. Advances in Applied Science Research 6(6), 114-124.

Ulgen N, Ozilgen M. 1993. Determination of optimum pH and temperature for pasteurization of citrus juices by response surface methodology. Zeitschrift für Lebensmittel-Untersuchung und -Forschung 196(1), 45-8.

Worthington Enzyme Manual. Enzymes and related biochemical. Charles C. Worthington, 1988.