Identification and characterization of the omaA gene encoding the major outer membrane protein of Azospirillum brasilense

被引:13
作者
Burdman, S
De Mot, R
Vanderleyden, J
Okon, Y
Jurkevitch, E
机构
[1] Hebrew Univ Jerusalem, Fac Agr Food & Environm Qual Sci, Dept Microbiol & Plant Pathol, IL-76100 Rehovot, Israel
[2] Hebrew Univ Jerusalem, Fac Agr Food & Environm Qual Sci, Otto Warburg Ctr Agr Biotechnol, IL-76100 Rehovot, Israel
[3] Katholieke Univ Leuven, Fac Agr & Appl Biol Sci, FA Janssens Lab Genet, B-3001 Heverlee, Belgium
来源
DNA SEQUENCE | 2000年 / 11卷 / 3-4期
基金
以色列科学基金会;
关键词
Azospirillum; outer membrane proteins (OMPs); major outer membrane protein (MOMP); porins;
D O I
10.3109/10425170009033236
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The major outer membrane protein (MOMP) of Azospirillum brasilense was purified and degenerate oligonucleotides were constructed on the basis of partial internal amino acid sequences. PCR products were obtained using total DNA of A.brasilense as template. One of these, a 766-bp fragment, was DIG-labelled and used in Southern hybridization against A. brasilense DNA and a genomic library of A. brasilense in Escherichia coli. A clone containing a 20-kb EcoRI insert in pLAFR3 was identified by PCR screening. From this insert, an EcoRI-SalI fragment of approximately 3.5-kb was subcloned in pUC19. The gene encoding the A.brasilense MOMP was sequenced and analyzed. The deduced amino acid sequence contains a putative signal peptide of 23 residues, followed by 367 amino acids of the mature protein with a molecular mass of 38,753 Da. The deduced amino acid sequence shows similarity to certain bacterial porins.
引用
收藏
页码:225 / 237
页数:13
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