Segura Daniel, Cruz Tania, Espín Guadalupe
Instituto de Biotecnología, Universidad Nacional Autónoma de México, Departamento de Microbiología Molecular, Apartado Postal 510-3, 62271 Cuernavaca, Morelos, México.
Arch Microbiol. 2003 Jun;179(6):437-43. doi: 10.1007/s00203-003-0553-4. Epub 2003 May 6.
The lipids poly-beta-hydroxybutyrate (PHB) and alkylresorcinols are the major metabolic products of Azotobacter vinelandii cysts. Cysts are formed in less than 0.01% of late stationary phase cells grown on sucrose. Culturing vegetative cells in n-butanol or beta-hydroxybutyrate induces encystment. After induction of encystment, PHB rapidly accumulates in large granules. Then, the cells begin the synthesis of alkylresorcinols that replace the phospholipids in the membranes and are components of the exine, the outer layer of the cyst envelope. Vegetative cells do not synthesize alkylresorcinols. We report here the effect of mutations in the phbBAC operon, coding for the enzymes of the PHB biosynthetic pathway, on the synthesis of alkylresorcinols and cyst formation. The phb mutations did not impair the capacity to form mature cysts. However, the cysts formed by these strains posses a thicker exine layer and a higher content of alkylresorcinols than the cysts formed by the wild-type strain. A blockage of PHB synthesis caused by phb mutations resulted in the synthesis of alkylresorcinols and encystment even under non-inducing conditions. We propose that, as a consequence of the blockage in the PHB biosynthetic pathway, the acetyl-CoA and reducing power pools are increased causing the shift to lipid metabolism required for the synthesis of alkylresorcinols and cyst formation.
脂质聚-β-羟基丁酸酯(PHB)和烷基间苯二酚是维涅兰德固氮菌孢囊的主要代谢产物。在以蔗糖为培养基生长的稳定期末期细胞中,形成孢囊的细胞比例不到0.01%。在正丁醇或β-羟基丁酸中培养营养细胞会诱导孢囊形成。诱导孢囊形成后,PHB迅速在大颗粒中积累。然后,细胞开始合成烷基间苯二酚,烷基间苯二酚会取代细胞膜中的磷脂,并且是孢囊包膜外层孢粉素的组成成分。营养细胞不合成烷基间苯二酚。我们在此报告了编码PHB生物合成途径中酶的phbBAC操纵子突变对烷基间苯二酚合成和孢囊形成的影响。phb突变并不损害形成成熟孢囊的能力。然而,这些菌株形成的孢囊比野生型菌株形成的孢囊具有更厚的孢粉素层和更高的烷基间苯二酚含量。phb突变导致的PHB合成受阻,即使在非诱导条件下也会导致烷基间苯二酚的合成和孢囊形成。我们提出,由于PHB生物合成途径的阻断,乙酰辅酶A和还原力库增加,导致转向烷基间苯二酚合成和孢囊形成所需的脂质代谢。