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Original Research Article | OPEN ACCESS

Purification and characterization of an antimicrobial protein from Gastrodia elata Blume tubers

Chen Chen1,2, Xinxin Li1,2, Jing Li1,2, Youmei Xu1,2, Xian Jing1, Sanqiao Wu1, Xiang Liu1,2, Xiaoying Zhang1,3

1Chinese-German Joint Laboratory for Natural Product Research, Qinling-Bashan Mountains Bioresources Comprehensive Development CIC, College of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong 723001; 2Shaanxi Engineering Research Center of Tall Gastrodia Tuber and Medical Dogwood, Hanzhong 723001; 3College of Veterinary Medicine, Northwest A&F University, Yangling 712100, China.

For correspondence:-  Xiaoying Zhang   Email: zhang.xy@nwsuaf.edu.cn   Tel:+869162641661

Accepted: 23 August 2018        Published: 30 September 2018

Citation: Chen C, Li X, Li J, Xu Y, Jing X, Wu S, et al. Purification and characterization of an antimicrobial protein from Gastrodia elata Blume tubers. Trop J Pharm Res 2018; 17(9):1717-1723 doi: 10.4314/tjpr.v17i9.5

© 2018 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To purify and characterize a novel antimicrobial protein from the Gastrodia elata Blume (Bl.) plant, which has long been used in herbal medicine.
Methods:  The procedure for isolation and purification of Gastrodia elata protein (GEP) involved phosphate buffer extraction, ammonium sulfate precipitation, ion-exchange chromatography, and gel-filtration chromatography. Sodium dodecyl sulfate - polyacrylamide gel electrophoresis was employed to detect the apparent molecular mass and determine homogeneity, while paper disc diffusion was used to measure the antibacterial activity of GEP. A hemolytic assay was performed on rabbit red blood cells. The effect of pH, salt concentration, and temperature on the antibacterial activity of GEP was evaluated by minimum inhibitory concentration assay.
Results: GEP was a 14-kDa monomer and displayed antimicrobial activity against Staphylococcus aureus and Candida albicans, with 8.0-mm and 9.4-mm zones of inhibition, respectively, but no antibacterial activity was observed against Escherichia coli. GEP had little hemolytic activity on red blood cells even at a concentrations of up to 200 mg/ml. GEP was thermally stable at temperatures below 70 °C for 30 min, and displayed higher antibacterial activity in the pH range 5.0 to 7.0.
Conclusion: GEP protein is relatively thermostable and possesses antimicrobial activity. The results suggest that GEP protein has potential agricultural and industrial applications, such as in transgenic plants.

Keywords: Antimicrobial protein, Gastrodia elata, Protein characterization

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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