Cloning and Identification of frc Gene from Oxalobacter Frmigenes
- Author:
Debo KONG
1
;
Zhiqiang CHEN
;
Zhangqun YE
;
Weimin YANG
;
Linfang YAO
;
Hui GUO
;
Guanlin LIU
;
Lingqi ZENG
Author Information
1. 华中科技大学同济医学院附属同济医院
- Keywords:
oxalobacter;
frc;
urolithiasis;
gene cloningKONG Debo,male,born in 1978,Candidate for Doctoral Degree
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2007;27(2):190-192
- CountryChina
- Language:Chinese
-
Abstract:
The cloning and identification of frc gene from Oxalobacter formigenes in the intestines of Chinese people were conducted. The genomic DNA of Oxalobacter formigenes was extracted. frc gene fragment was amplified by polymerase chain reaction (PCR) and linked with pEGFP-C1. The recombinant plasmid was designated pEGFP-frc and was identified by restriction-enzyme digestion and sequencing. Human embryo kidney 293 cells were transfected with pEGFP-frc, then RT-PCR and Western blotting were performed to detect the expression offrc gene. The length of frc gene was found to be 1287 bp, and the homology of nucleotides and amino-acid residue with the sequence in GenBank was 95.88% and 99.07%. Bright green fluorescent light could be observed in 293 cells transfected with the pEGFP-frc. frc mRNA and fusion protein FCoAT-EGFP were detected in the cells. It is concluded that frc gene cloned from the Oxalobacterformigenes in the intestines of Chinese people can be expressed in eucaryotic 293 cells and keep its enzyme activity.
