Lee Kyoung, Lim Eun Jin, Kim Keun Soo, Huang Shir-Ly, Veeranagouda Yaligara, Rehm Bernd H A
Department of Microbiology and Biomedical Science Institute at CWNU, Changwon National University, Changwon-si, Kyongnam, 641-773, South Korea,
Appl Microbiol Biotechnol. 2014 May;98(9):4137-48. doi: 10.1007/s00253-014-5529-6. Epub 2014 Feb 4.
Pseudomonas alkylphenolia is known to form different types of multicellular structures depending on the environmental stimuli. Aerial structures formed during vapor p-cresol utilization are unique. Transposon mutants that showed a smooth colony phenotype failed to form a differentiated biofilm, including aerial structures and pellicles, and showed deficient surface spreading motility. The transposon insertion sites were located to a gene cluster designated epm (extracellular polymer matrix), which comprises 11 ORFs in the same transcriptional orientation. The putative proteins encoded by the genes in the epm cluster showed amino acid sequence homology to those found in the alginate biosynthesis gene clusters, e.g., in Pseudomonas aeruginosa at similarity levels of 32.3-86.4 %. This overall resemblance indicated that the epm gene cluster encodes proteins that mediate the synthesis of an exopolysaccharide composed of uronic acid(s) similar to alginate. Our preliminary results suggested that the epm-derived polymer is a substituted polymannuronic acid. Gene clusters homologous to the epm gene cluster are found in the genomes of a few species of the genera Pseudomonas, Alcanivorax, and Marinobacter. A mutational analysis showed that the epmJ and epmG genes encoding putative exopolysaccharide-modifying enzymes are required to form multicellular structures. An analysis of the activity of the promoter P epmD using a transcriptional fusion to the green fluorescence protein gene showed that the epm genes are strongly expressed at the tips of the specialized aerial structures. Our results suggested that the epm gene cluster is involved in the formation of a scaffold polysaccharide that is required to form multicellular structures in P. alkylphenolia.
已知烷基酚假单胞菌会根据环境刺激形成不同类型的多细胞结构。在利用对甲酚蒸汽过程中形成的气生结构很独特。表现出光滑菌落表型的转座子突变体无法形成分化的生物膜,包括气生结构和菌膜,且表面扩散运动能力不足。转座子插入位点定位于一个名为epm(细胞外聚合物基质)的基因簇,该基因簇由11个转录方向相同的开放阅读框组成。epm基因簇中的基因编码的推定蛋白质与藻酸盐生物合成基因簇中的蛋白质具有氨基酸序列同源性,例如在铜绿假单胞菌中,相似性水平为32.3 - 86.4%。这种总体相似性表明,epm基因簇编码介导类似于藻酸盐的由糖醛酸组成的胞外多糖合成的蛋白质。我们的初步结果表明,epm衍生的聚合物是一种取代的聚甘露糖醛酸。在假单胞菌属、食烷菌属和海杆菌属的一些物种的基因组中发现了与epm基因簇同源的基因簇。突变分析表明,编码推定胞外多糖修饰酶的epmJ和epmG基因是形成多细胞结构所必需的。使用与绿色荧光蛋白基因的转录融合对启动子P epmD的活性进行分析表明,epm基因在特化气生结构的顶端强烈表达。我们的结果表明,epm基因簇参与了烷基酚假单胞菌形成多细胞结构所需的支架多糖的形成。