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Purification and characterization of phosphoenolpyruvate carboxykinase from Raillietina echinobothrida, a cestode parasite of the domestic fowl

Published online by Cambridge University Press:  20 August 2012

B. DAS ,
V. TANDON ,
J. K. SAXENA ,
S. JOSHI  and
A. R. SINGH
B. DAS
Affiliation:
Department of Zoology, North Eastern Hill University, Shillong-793022, India
V. TANDON*
Affiliation:
Department of Zoology, North Eastern Hill University, Shillong-793022, India
J. K. SAXENA
Affiliation:
Biochemistry Division, Central Drug Research Institute, Lucknow-226001, India
S. JOSHI
Affiliation:
Biochemistry Division, Central Drug Research Institute, Lucknow-226001, India
A. R. SINGH
Affiliation:
Biochemistry Division, Central Drug Research Institute, Lucknow-226001, India
*
*Corresponding author: Department of Zoology, North Eastern Hill University, Shillong-793022, India. Tel: +91 364 2722312. Fax: +91 364 2550300/2550108. E-mail: tandonveena@gmail.com
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Summary

Phosphoenolpyruvate carboxykinase (PEPCK, EC 4.1.1.32) is an essential regulatory enzyme of glycolysis in helminths in contrast to its role in gluconeogenesis in their host. Previously we have reported that phytochemicals from Flemingia vestita (Family: Fabaceae), genistein in particular, have vermifugal action and are known to affect carbohydrate metabolism in the cestode, Raillietina echinobothrida. In order to determine the functional differences of PEPCK from the parasite and its avian host (Gallus domesticus), we purified the parasite enzyme apparently to homogeneity, and characterized it. The native PEPCK is a monomer with a subunit molecular weight of 65 kDa. The purified enzyme displayed standard Michaelis-Menten kinetics with Km value of 42·52 μM for its substrate PEP. The Ki for the competitive inhibitors GTP, GMP, ITP and IMP for the carboxylation reaction were determined and discussed. In order to identify putative modulators from plant sources, phytochemicals from F. vestita and Stephania glabra were tested on the purified PEPCK, which resulted in alteration of its activity. From our results, we hypothesize that PEPCK may be a potential target site for anthelmintic action.

Keywords

PEPCKcestodeRaillietina echinobothridaFlemingia vestitagenisteinStephania glabra
Type
Research Article
Information
Parasitology , Volume 140 , Issue 1 , January 2013 , pp. 136 - 146
Copyright
Copyright © Cambridge University Press 2012

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