Department of Biology, Utah State University, Logan, Utah 84322-5305.
Appl Environ Microbiol. 1998 Jan;64(1):226-30. doi: 10.1128/AEM.64.1.226-230.1998.
Many strains of Pseudomonas syringae pv. syringae produce one of four classes of small cyclic lipodepsinonapeptides: syringomycins, syringostatins, syringotoxins, or pseudomycins. These metabolites are phytotoxic and growth inhibitory against a broad spectrum of fungi. Their production is dependent upon the expression of conserved biosynthesis and export genes syrB and syrD, respectively. PCR and oligonucleotide primers specific for a 752-bp fragment of syrB were used to identify cyclic lipodepsinonapeptide-producing strains of P. syringae pv. syringae. In contrast, PCR amplification with primers based on syrD did not always correlate with possession of the syrD gene, as indicated by Southern blot analysis, or with cyclic lipodepsinonapeptide production. Sequence comparisons of 400 nucleotides from the syrB PCR-amplified fragments showed 94% plot similarity among 27 strains. In a sequence phenogram, syringostatin and syringotoxin producers were grouped apart from syringomycin-producing strain B301D, with sequences that differed by eight and nine conserved base substitutions, respectively. PCR amplification of the 752-bp syrB fragment offers rapid and accurate detection of cyclic lipodepsinonapeptide-producing strains, and its sequence provides some predictive capabilities for identifying syringotoxin and syringostatin producers.
许多丁香假单胞菌 pv. 丁香假单胞菌菌株产生四类小环脂肽脂肽类化合物之一:丁香霉素、丁香菌素、丁香毒素或假霉素。这些代谢物对广泛的真菌具有植物毒性和生长抑制作用。它们的产生依赖于保守的生物合成和出口基因 syrB 和 syrD 的表达。分别使用针对 syrB 的 752-bp 片段的 PCR 和寡核苷酸引物来鉴定丁香假单胞菌 pv. 丁香假单胞菌的环脂肽类化合物产生菌株。相比之下,基于 syrD 的引物的 PCR 扩增并不总是与 syrD 基因的存在相关,如 Southern 印迹分析所示,也与环脂肽类化合物的产生无关。来自 syrB PCR 扩增片段的 400 个核苷酸的序列比较显示 27 个菌株之间有 94%的相似性。在序列表型图中,丁香菌素和丁香毒素产生菌与丁香霉素产生菌 B301D 分开,它们的序列分别有八个和九个保守碱基取代的差异。752-bp syrB 片段的 PCR 扩增提供了快速准确的环脂肽类化合物产生菌检测方法,其序列为鉴定丁香毒素和丁香菌素产生菌提供了一些预测能力。