Lipasova V A, Atamova E E, Veselova M A, Tarasova N N, Khmel' I A
Genetika. 2009 Jan;45(1):38-42.
The introduction into strain Pseudomonas chlororaphis 449 of plasmid pME6863 that contains the cloned gene for N-acyl-homoserine lactonase, AiiA, leads to the degradation of all three types of N-acyl-homoserine lactones produced by this strain (N-butanoyl-L-homoserine lactone, N-hexanoyl-homoserine lactone, and N-3-oxo-hexanoyl-homoserine lactone). This causes a drastic reduction in the synthesis of phenazine pigment and decreases the ability of cells to migrate on the surface of nutrient medium. However, the antagonistic activity of P. chlororaphis 449 toward phytopathogenic fungi Sclerotinia sclerotiorum and Rhizoctonia solani is not only decreased, but is even slightly increased; no essential changes in the exoprotease activity were observed. It is assumed that one of the QS systems of P. chlororaphis 449 may exert the repression effect on the expression of genes, which determine the two latter cell activities.
将含有N - 酰基高丝氨酸内酯酶AiiA克隆基因的质粒pME6863导入绿针假单胞菌449菌株后,该菌株产生的三种类型的N - 酰基高丝氨酸内酯(N - 丁酰基 - L - 高丝氨酸内酯、N - 己酰基高丝氨酸内酯和N - 3 - 氧代己酰基高丝氨酸内酯)都会被降解。这导致吩嗪色素的合成大幅减少,并降低细胞在营养培养基表面迁移的能力。然而,绿针假单胞菌449对植物病原真菌核盘菌和立枯丝核菌的拮抗活性不仅没有降低,甚至略有增加;未观察到胞外蛋白酶活性有本质变化。据推测,绿针假单胞菌449的一种群体感应系统可能对决定后两种细胞活性的基因表达产生抑制作用。