Gaisser S, Hughes C
University of Cambridge, Department of Pathology, UK.
Mol Gen Genet. 1997 Jan 27;253(4):415-27. doi: 10.1007/s004380050339.
We describe a large bacterial locus that, unusually, encodes components typically required for both the non-ribosomal synthesis of peptides and also polyketide/fatty acid synthase function. Two tandem ABC transporter genes in this putative nrp (non-ribosomal peptide/polyketide) operon suggest that the principal product may be secreted. Immediately distal to the nrp operon is a gene, irpP, encoding a small peptide similar to the Bacillus ComX pheromone that in its mature, extracellular form increases expression of unlinked non-ribosomal peptide synthesis genes. Transcription of both the nrp operon and irpP was up-regulated in iron-limiting culture conditions, consistent with the presence of a putative Fur repressor-binding site 5' of irpP. The locus was isolated from Proteus mirabilis as the site of a TnphoA insertion causing impaired swarm cell differentiation and an aberrant swarming pattern. The mutation was in one of the transporter genes, but a comparable swarming defect resulted from interposon disruption of the putative nrp synthetase gene.
我们描述了一个大型细菌基因座,该基因座不同寻常地编码了肽的非核糖体合成以及聚酮/脂肪酸合酶功能通常所需的成分。这个假定的nrp(非核糖体肽/聚酮)操纵子中的两个串联ABC转运蛋白基因表明主要产物可能会被分泌。在nrp操纵子的紧邻下游是一个基因irpP,它编码一种与芽孢杆菌ComX信息素相似的小肽,其成熟的细胞外形式会增加未连锁的非核糖体肽合成基因的表达。在铁限制培养条件下,nrp操纵子和irpP的转录均上调,这与irpP 5'端存在一个假定的Fur阻遏物结合位点一致。该基因座是从奇异变形杆菌中分离出来的,作为TnphoA插入的位点,该插入导致群体细胞分化受损和异常的群体运动模式。突变发生在其中一个转运蛋白基因中,但转座子破坏假定的nrp合成酶基因也导致了类似的群体运动缺陷。