Isolation, sequencing and expression of the gene encoding a major protein from the backteriophage associated with Bartonella henselae

被引:22
作者
Bowers, TJ
Sweger, D
Jue, D
Anderson, B [1 ]
机构
[1] Univ S Florida, Coll Med, Dept Med Microbiol & Immunol, Tampa, FL 33612 USA
[2] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
关键词
cat scratch disease; transduction; gene cloning; signal peptide;
D O I
10.1016/S0378-1119(97)00580-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The gene encoding a 31-kDa major protein (Pap31) associated with the bacteriophage harbored in Bartonella henselae was cloned and sequenced. Analysis of the resulting sequence revealed an open reading frame of 837 nucleotides coding for a protein of 279 amino acids. pap31 was then subcloned downstream of the lacZ promoter in pUC19. pap31 was amplified by polymerase chain reaction, and the linear amplicon was used as template for in-vitro transcription and translation. A protein with an apparent molecular mass of approximately 31 kDa was synthesized from this reaction. Upon analysis of the deduced aa sequence, a potential signal sequence and a consensus signal peptidase cleavage site were identified, indicative that Pap31 is modified posttranslationally, and the mature protein may be targeted to the host membrane. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:49 / 52
页数:4
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