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伯氏疏螺旋体超氧化物歧化酶基因的转录分析

Transcriptional analysis of a superoxide dismutase gene of Borrelia burgdorferi.

作者信息

Nichols T L, Whitehouse C A, Austin F E

机构信息

Department of Microbiology and Immunology, University of Louisville, School of Medicine, Louisville, KY, USA.

出版信息

FEMS Microbiol Lett. 2000 Feb 1;183(1):37-42. doi: 10.1111/j.1574-6968.2000.tb08930.x.

Abstract

A single superoxide dismutase (Sod) gene was identified in Borrelia burgdorferi strains, Borrelia afzelii Ple and Borrelia garinii Pbi. Recombinant enzymatic activity was detected only when sod expression was controlled by the lacZ promoter in the cloning vector. Northern blot analysis with sod- or secA-specific probes identified a common 3.7-kb transcript. Reverse transcriptase-PCR analysis confirmed that secA and sod constitute a single transcriptional unit in B. burgdorferi. A transcriptional start site of this operon, containing -10 and -35 regions of a sigma(70)-type promoter, was mapped to 100 bp upstream of the ATG start codon of secA.

摘要

在伯氏疏螺旋体菌株、阿氏疏螺旋体Ple和伽氏疏螺旋体Pbi中鉴定出一个超氧化物歧化酶(Sod)基因。仅当克隆载体中的sod表达由lacZ启动子控制时,才能检测到重组酶活性。用sod或secA特异性探针进行的Northern印迹分析鉴定出一个常见的3.7kb转录本。逆转录酶-PCR分析证实,secA和sod在伯氏疏螺旋体中构成一个单一的转录单元。该操纵子的转录起始位点包含一个σ(70)型启动子的-10和-35区域,被定位到secA的ATG起始密码子上游100bp处。

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