Cloning and Sequence Analysis of the Gene Encoding LipL32 of Leptospira interrogans Serovar Sejroe

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作者
R. Amutha
P. Chaudhury
Amar P. Garg
P. Vasan
P. S. Cheema
S. K. Srivastava
机构
[1] Indian Veterinary Research Institute,Division of Bacteriology and Mycology
[2] Ch. Charan Singh University,Department of Microbiology
[3] Madras Veterinary College,Department of Animal Nutrition
[4] Tanuvas,undefined
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关键词
leptospirosis; LipL32 cloning;
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摘要
Leptospira, a member of the order Spirochaetales, is the causative agent of leptospirosis, an important zoonosis encountered worldwide. The Leptospira interrogans serovar Sejroe was grown in EMJH medium and its DNA was isolated using standard techniques. The LipL32 gene was amplified using the reported primer of Kirschneri of LipL32. The amplified product was found to comprise 756 base pairs. This amplified gene fragment of LipL32 lipoprotein was cloned in E. coli (DH5α) cells using pDrive plasmid as a vector. The recombinant cells were selected on LB agar medium containing ampicillin, X-gal and isopropyl-β-d-thiogalactopyranoside. Plasmid was extracted from the recombinant white colonies, and restriction endonuclease (RE) analysis was carried out using PstI and SalI. On partial sequence analysis, the product exhibited 756 base pairs, corresponding to 251 amino acids. The cloned gene could be further used for expression of recombinant protein for serodiagnosis of leptospirosis.
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页码:513 / 519
页数:6
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