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猪链球菌srt基因的同源性分析及srtA的原核表达

[Homologous analysis of Streptococcus suis srt gene and prokaryotic expression of srtA].

作者信息

Dong Ya-qing, Wang Chang-jun, Zheng Feng, Pan Xiu-zhen, Fan Hong-jie, Tang Jia-qi

机构信息

College of Veterinary Medicine, Nanjing Agriculture University, Nanjing 210095, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2007 May;23(5):399-401.

Abstract

AIM

To elucidate the distribution of srt gene in the genome of S.suis 05ZYH33, prokaryotically express Sortase A and analyze its antigenicity.

METHODS

Homologous genes encoding sortase family members were analyzed, and then the srtA gene of S.suis was cloned and sequenced. The recombinant protein was analyzed by SDS-PAGE and Western blot. The mice were immunized with recombinant protein and the antibody titer was determined by indirect ELISA.

RESULTS

All the putative srt genes in the genome of 05ZYH33 were analyzed. Six genes were found to be homologous to srt of S.suis isolated in Japan. The predicted srtA and sortase-like proteins were members of Class A of sortase family while srtBCD and srtE belonged to Class B. Western blot analysis showed that the recombinant protein was reactive to with the serum from the rabbits infected with a virulent strain of S.suis Type 2. The antibody titer in blood serum reached 1:6 400 after immunization with recombinant protein four times.

CONCLUSION

Compared with the isolated strain from Japan a new putative srt gene was found in 05ZYH33. The srtA gene was successfully expressed in prokaryotic system and the recombinant protein showed specific antigenicity, which is important for future research of the function of Sortase.

摘要

目的

阐明srt基因在猪链球菌05ZYH33基因组中的分布,原核表达分选酶A并分析其抗原性。

方法

分析编码分选酶家族成员的同源基因,然后克隆并测序猪链球菌的srtA基因。通过SDS-PAGE和Western blot分析重组蛋白。用重组蛋白免疫小鼠,通过间接ELISA测定抗体效价。

结果

分析了05ZYH33基因组中所有推测的srt基因。发现6个基因与日本分离的猪链球菌的srt基因同源。预测的srtA和类分选酶蛋白属于分选酶家族A类,而srtBCD和srtE属于B类。Western blot分析表明,重组蛋白与感染强毒株猪链球菌2型的兔血清有反应。用重组蛋白免疫4次后,血清中的抗体效价达到1:6400。

结论

与日本分离株相比,在05ZYH33中发现了一个新的推测srt基因。srtA基因在原核系统中成功表达,重组蛋白具有特异性抗原性,这对未来分选酶功能的研究具有重要意义。

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