Liu Y, Chatterjee A, Chatterjee A K
Department of Plant Pathology, University of Missouri, Columbia 65211.
Appl Environ Microbiol. 1994 Jul;60(7):2545-52. doi: 10.1128/aem.60.7.2545-2552.1994.
Our previous genetic analysis (J. W. Willis, J. K. Engwall, and A. K. Chatterjee, Phytopathology 77:1199-1205, 1987) had revealed a tight linkage between pel-3 (pel, pectate lyase gene) and peh-1 (peh, polygalacturonase gene) within the chromosome of Erwinia carotovora subsp. carotovora 71. Nucleotide sequencing, transcript assays, and expression of enzymatic activities in Escherichia coli have now confirmed that a 3,500-bp segment contains the open reading frames (ORFs) for Pel-3 and Peh-1. The 1,041-bp pel-3 ORF and the 1,206-bp peh-1 ORF are separated by a 579-bp sequence. The genes are transcribed divergently from their own promoters. In E. coli and E. carotovora subsp. carotovora 71, peh-1 is better expressed than pel-3. However, plant signals activate the expression of both the genes in E. carotovora subsp. carotovora. A consensus integration host factor (IHF)-binding sequence upstream of pel-3 appears physiologically significant, since pel-3 promoter activity is higher in an E. coli IHF+ strain than in an IHF- strain. While peh-1 has extensive homology with plant and bacterial peh genes, pel-3 appears not to have significant homology with the pel genes belonging to the pelBC, pelADE, or periplasmic pel families. Pel-3 also is unusual in that it is predicted to contain an ATP- and GTP-binding site motif A (P-loop) not found in the other Pels.
我们之前的遗传分析(J. W. 威利斯、J. K. 恩格沃尔和A. K. 查特吉,《植物病理学》77:1199 - 1205,1987)表明,胡萝卜软腐欧文氏菌胡萝卜软腐亚种71染色体上的果胶酸裂解酶基因(pel-3)和多聚半乳糖醛酸酶基因(peh-1)之间存在紧密连锁。核苷酸测序、转录分析以及在大肠杆菌中的酶活性表达现已证实,一个3500 bp的片段包含Pel-3和Peh-1的开放阅读框(ORF)。1041 bp的pel-3 ORF和1206 bp的peh-1 ORF被一个579 bp的序列隔开。这些基因从各自的启动子开始以不同方向转录。在大肠杆菌和胡萝卜软腐欧文氏菌胡萝卜软腐亚种71中,peh-1的表达优于pel-3。然而,植物信号可激活胡萝卜软腐欧文氏菌胡萝卜软腐亚种中这两个基因的表达。pel-3上游的一个共有整合宿主因子(IHF)结合序列似乎具有生理意义,因为在大肠杆菌的IHF +菌株中pel-3启动子活性高于IHF -菌株。虽然peh-1与植物和细菌的peh基因具有广泛同源性,但pel-3似乎与属于pelBC、pelADE或周质pel家族的pel基因没有显著同源性。Pel-3的不同寻常之处还在于,预计它含有一个在其他果胶酸裂解酶中未发现的ATP和GTP结合位点基序A(P环)。