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Cloning, Expression and Molecular Characterization of Glutathione Transferase P1-1 Gene from the Camel, Camelus dromedarius
被引:0
|作者:
Ataya, Farid S.
[1
,2
]
Fouad, Dalia
[3
,4
]
Malik, Ajamaluddin
[1
]
Labrou, Nikolaos E.
[5
]
Daoud, Mohamed S.
[1
,6
]
Saeed, Hesham M.
[7
]
机构:
[1] King Saud Univ, Coll Sci, Dept Biochem, POB 2455, Riyadh 11451, Saudi Arabia
[2] Natl Res Ctr, Genet Engn Div, Mol Biol Dept, 33 El Bohouth St,PO 1262, Giza, Egypt
[3] King Saud Univ, Coll Sci, Dept Zool, PO 22452, Riyadh 11459, Saudi Arabia
[4] Helwan Univ, Fac Sci, Dept Zool & Entomol, Cairo, Egypt
[5] Agr Univ Athens, Sch Food Biotechnol & Dev, Dept Biotechnol, Lab Enzyme Technol, 75 Iera Odos St, GR-11855 Athens, Greece
[6] Cairo Univ, Kasr Al Ainy Univ Hosp, Dept Clin & Chem Pathol, King Fahd Unit Lab, Cairo 11562, Egypt
[7] Alexandria Univ, Inst Grad Studies & Res, Dept Biotechnol, Alexandria, Egypt
关键词:
One-humped camel;
GST-pi;
Gene expression;
Molecular modelling;
Cloning;
Phylogenetic analysis;
N-CAPPING BOX;
S-TRANSFERASE;
ENZYME;
ALPHA;
ISOENZYMES;
IDENTIFICATION;
ACTIVATION;
PROTEINS;
KAPPA;
THIOL;
D O I:
10.17582/journal.pjz/2017.49.6.2279.2289
中图分类号:
Q95 [动物学];
学科分类号:
071002 ;
摘要:
In this study, we report the cloning, expression and characterization of the glutathione transferase isoenzyme P1-1 gene from Camelus dromedarius (CdGSTP1-1). The coding sequence was cloned using RT-PCR. Sequence analysis demonstrated significant differences between amino acid sequence of C. dromedarius and other mammalian GSTP1-1 enzymes. Phylogenetic relationship was studied with different organisms belonging to animal kingdom and revealed that CdGSTP1-1 is grouped with the enzyme from S. scrofa. The 3D homology model of CdGSTP1-1 showed similar fold and topology with the porcine GSTpi enzyme. Gene expression analysis in five camel tissues was examined employing real-time PCR. The highest level of transcripts was found in the camel testis, followed by liver, spleen, kidney and lung. CdGSTP1-1 was heterologously expressed in Eschericia colt BL21(DE3) as a 24 kDa soluble protein and showed to be catalyticly active towards the model substrate 1-chloro-2,4-dinitrobenzene. The results of the present study provide new information into camelid evolution and give further insights into the diversity and complex enzymatic functions of GST superfamily.
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页码:2279 / 2289
页数:11
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