Aldridge P, Metzger M, Geider K
Max-Planck-Institut für Zellbiologie, Ladenburg, Germany.
Mol Gen Genet. 1997 Nov;256(6):611-9. doi: 10.1007/s004380050609.
A chromosomal DNA fragment from Erwinia amylovora was identified that complemented a deletion mutant in the gut(srl) operon of Escherichia coli. The E. amylovora srl operon on the cloned fragment was localized by transposon mutagenesis. A DNA fragment including the srl genes of E. amylovora was sequenced and found to contain six open reading frames (ORFs). These ORFs were highly homologous to genes of the gut operon of E. coli. No large gene was found that encoded a protein equivalent to GutA of E. coli; instead two ORFs with extensive similarity to GutA were identified in the E. amylovora srl operon. All transposon insertions were mapped by PCR analysis, and several insertions in a plasmid bearing the srl operon were unable to complement a mutation in the E. coli gutD gene. All E. amylovora srl mutants could be complemented by introducing the sorbitol operon from E. coli. The direction of transcription was confirmed by analysis of lacZ fusions. Expression of the srl operon in E. amylovora was high in the presence of sorbitol in the medium and was repressed by glucose. Mutants with a sorbitol deficiency were still virulent on slices of immature pears, but were unable to cause significant fire blight symptoms on apple shoots. Since sorbitol is used for carbohydrate transport in host plants of E. amylovora, this sugar alcohol may be an important factor in determining host specificity for the fire blight pathogen.
鉴定出了来自梨火疫病菌的一个染色体DNA片段,该片段可互补大肠杆菌肠道(srl)操纵子中的一个缺失突变体。通过转座子诱变确定了克隆片段上梨火疫病菌的srl操纵子的位置。对包含梨火疫病菌srl基因的一个DNA片段进行了测序,发现其含有六个开放阅读框(ORF)。这些ORF与大肠杆菌肠道操纵子的基因高度同源。未发现编码与大肠杆菌GutA等效蛋白质的大基因;相反,在梨火疫病菌srl操纵子中鉴定出了两个与GutA具有广泛相似性的ORF。通过PCR分析对所有转座子插入进行了定位,携带srl操纵子的质粒中的几个插入无法互补大肠杆菌gutD基因中的突变。通过导入来自大肠杆菌的山梨醇操纵子,所有梨火疫病菌srl突变体均可得到互补。通过对lacZ融合体的分析证实了转录方向。在培养基中存在山梨醇的情况下,梨火疫病菌中srl操纵子的表达很高,并且受到葡萄糖的抑制。山梨醇缺乏的突变体在未成熟梨切片上仍具有毒性,但在苹果嫩枝上无法引起明显的火疫病症状。由于山梨醇用于梨火疫病菌宿主植物中的碳水化合物运输,这种糖醇可能是决定火疫病病原菌宿主特异性的一个重要因素。