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沙眼衣原体热休克蛋白10的克隆与序列分析

[Cloning and sequence analysis of Chlamydia trachomatis heat shock protein 10].

作者信息

Zhang Hong-Ye, Lu Jin-Chun

机构信息

Clinical Laboratory, Nanjing Yuhua Hospital, Nanjing, Jiangsu 210012, China.

出版信息

Zhonghua Nan Ke Xue. 2003 Dec;9(9):687-9.

PMID:14727360
Abstract

OBJECTIVE

To obtain Chlamydia trachomatis heat shock protein (cHSP) 10 gene from clinical secretion samples.

METHODS

cHSP10 gene was amplified from 20 cases of clinical secretion samples with positive gold-labelling by specific primers of cHSP10 and identified by sequence analysis.

RESULTS

cHSP10 full-length gene was amplified from 1 of 20 cases of clinical secretion samples with positive gold-labelling. cHSP10 gene encoding 102 amino acids contains 306 bp, which nuclotide at position 194 changes from T to A, leading to the change of corresponding amino acid.

CONCLUSIONS

cHSP10 gene may be cloned from clinical secretion samples with positive gold-labelling, which make it possible to further construct expression plasmid of recombinant cHSP10.

摘要

目的

从临床分泌物样本中获取沙眼衣原体热休克蛋白(cHSP)10基因。

方法

采用cHSP10特异性引物,从20例金标阳性的临床分泌物样本中扩增cHSP10基因,并进行序列分析鉴定。

结果

从20例金标阳性的临床分泌物样本中的1例扩增出cHSP10全长基因。cHSP10基因编码102个氨基酸,含306 bp,其中第194位核苷酸由T变为A,导致相应氨基酸改变。

结论

可从金标阳性的临床分泌物样本中克隆cHSP10基因,这为进一步构建重组cHSP10表达质粒奠定了基础。

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