Molecular cloning and functional characterization of a glucose transporter (CsGLUT) in Clonorchis sinensis
- Authors
- Ahn, Seong Kyu; Cho, Pyo Yun; Na, Byoung-Kuk; Hong, Sung-Jong; Nam, Ho-Woo; Sohn, Woon-Mok; Ardelli, Bernadette F.; Park, Yun-Kyu; Kim, Tong-Soo; Cha, Seok Ho
- Issue Date
- Jan-2016
- Publisher
- SPRINGER
- Keywords
- Glucose transporter; Clonorchis sinensis; Xenopus oocyst; Glucose uptake
- Citation
- PARASITOLOGY RESEARCH, v.115, no.1, pp 347 - 354
- Pages
- 8
- Journal Title
- PARASITOLOGY RESEARCH
- Volume
- 115
- Number
- 1
- Start Page
- 347
- End Page
- 354
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/7447
- DOI
- 10.1007/s00436-015-4754-y
- ISSN
- 0932-0113
1432-1955
- Abstract
- A complementary DNA (cDNA) encoding a glucose transporter of Clonorchis sinensis (CsGLUT) was isolated from the adult C. sinensis cDNA library. The open reading frame of CsGLUT cDNA consists of 1653 base pairs that encode a 550-amino acid residue protein. Hydropathy analysis suggested that CsGLUT possess 12 putative membrane-spanning domains. The Northern blot analysis result using poly(A)(+)RNA showed a strong band at similar to 2.1 kb for CsGLUT. When expressed in Xenopus oocytes, CsGLUT mediated the transport of radiolabeled deoxy-D-glucose in a time-dependent but sodium-independent manner. Concentration-dependency results showed saturable kinetics and followed the Michaelis-Menten equation. Nonlinear regression analyses yielded a Km value of 588.5 +/- 53.0 mu M and a Vmax value of 1500.0 +/- 67.5 pmol/oocyte/30 min for [1,2-H-3]2-deoxy-D-glucose. No trans-uptakes of bile acid (taurocholic acid), amino acids (tryptophan and arginine), or p-aminohippuric acid were observed. CsGLUT-mediated transport of deoxyglucose was significantly and concentration-dependently inhibited by radio-unlabeled deoxyglucose and D-glucose. 3-O-Methylglucose at 10 and 100 mu M inhibited deoxyglucose uptake by similar to 50 % without concentration dependence. No inhibitory effects by galactose, mannose, and fructose were observed. This work may contribute to the molecular biological study of carbohydrate metabolism and new drug development of C. sinensis.
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