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[牛分枝杆菌卡介苗抗原85-B信号肽基因的克隆与鉴定]

[Cloning and identification of the Mycobacterium bovis BCG gene for signal peptide of antigen 85-B].

作者信息

Zeng X, Wang G, Lu Y

机构信息

Department of Medical Molecular Biology, Tongji Medical University, Wuhan.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 1996 Dec;19(6):350-2.

PMID:9596817
Abstract

OBJECTIVE

To clone and identify the Mycobacterium bovis BCG gene for signal peptide of antigen 85-B.

METHODS

Using a polymerase chain reaction technique, the signal peptide sequence (position 94 to 211) of antigen 85-B was technique, which is one of the major protein secreted by Mycobacterium bovis BCG (Bacille-Calmette-Guerin). The gene of 117bp fragment was cloned into the SacI and EcoRI sites of pBluecript SK, and its sequence was determined by using T7DNA polymerase kit.

RESULTS

The sequence analysis showed that the sequence of 117bp signal peptide was not misincorporated and in 3' end understream of signal peptide the 12 multi cloning sites for foreign gene could be provided by the recombinant plasmid.

CONCLUSIONS

The signal sequence of BCG antigen 85-B was cloned into the pBluescript plasmid. The recombinant plasmid was called BCG-S01. According to the genetic information a secreted protein from M. bovis BCG could be utilized in making a useful vaccine vehicle to produce and secrete a vaccinal protein from M. bovis BCG living cells.

摘要

目的

克隆并鉴定牛分枝杆菌卡介苗(BCG)的抗原85-B信号肽基因。

方法

采用聚合酶链反应技术,扩增牛分枝杆菌卡介苗主要分泌蛋白之一抗原85-B的信号肽序列(第94至211位)。将117bp片段的基因克隆到pBluecript SK的SacI和EcoRI位点,并用T7DNA聚合酶试剂盒测定其序列。

结果

序列分析表明,117bp信号肽序列无误,重组质粒可在信号肽3'端下游提供12个外源基因多克隆位点。

结论

将卡介苗抗原85-B的信号序列克隆到pBluescript质粒中,构建的重组质粒命名为BCG-S01。根据遗传信息,牛分枝杆菌卡介苗的一种分泌蛋白可用于构建有效的疫苗载体,以便从牛分枝杆菌卡介苗活细胞中产生和分泌疫苗蛋白。

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