Quagliano J C, Miyazaki S S
Centro de Investigaciones Biotecnológicas en Microorganismos (CIBEM), Microbiología, Facultad de Agronomía, Universidad de Buenos Aires, Av. San Martín 4453 (1417), Buenos Aires, Argentina.
Appl Biochem Biotechnol. 1999 Dec;82(3):199-208. doi: 10.1385/abab:82:3:199.
Coproduction of poly-beta-hydroxybutyrate (PHB) and exopolysaccharides (EPS) was investigated with Azotobacter chroococcum strain 6B isolated from soil samples. The bacterium was cultured using various carbon sources solely or with 0.1 g/L of ammonium sulfate. Ammonium addition resulted in reduced PHB and EPS production with glucose, fructose, and sucrose media, but cellular mass remained constant except for sucrose. Protein was nearly twofold higher in ammonium-grown cultures. Glucose and fructose alone biosynthesized high amounts of EPS (maximum 2.1 and 1.1 g/L, respectively, at 72 h), whereas PHB was accumulated only in glucose-grown cells. Sucrose almost did not produce EPS. Conversely, PHB content was the highest obtained from all experimented conditions (1.1 g/L at 48 h, 40% cell dry wt). When a complex carbon source such as sugar cane molasses was utilized, PHB was accumulated concomitant with EPS production from the initial time to 48 h (0.75 g/L, 37% cell dry wt and 0.6 g/L, respectively), and then PHB decayed at 72 h (0.2 g/L). On the other hand, EPS continued to be biosynthesized (1.1 g/L, 72 h). PHB fractions of total intra- and extracellular biopolymers were calculated. Sucrose-modified Burk's medium without ammonium addition is suggested as a medium capable of diverting the carbon source for the production of intracellular PHB rather than EPS with A. chroococcum 6B.
利用从土壤样品中分离出的褐球固氮菌6B菌株,研究了聚-β-羟基丁酸酯(PHB)和胞外多糖(EPS)的联产情况。该细菌单独使用各种碳源或与0.1 g/L硫酸铵一起培养。添加铵会导致在葡萄糖、果糖和蔗糖培养基中PHB和EPS产量降低,但除蔗糖外细胞质量保持恒定。在铵培养的培养物中蛋白质含量几乎高出两倍。单独的葡萄糖和果糖能生物合成大量EPS(72 h时分别最高可达2.1 g/L和1.1 g/L),而PHB仅在葡萄糖培养的细胞中积累。蔗糖几乎不产生EPS。相反,在所有实验条件下获得的PHB含量最高(48 h时为1.1 g/L,占细胞干重的40%)。当使用甘蔗 molasses等复合碳源时,从初始时间到48 h,PHB与EPS的产生同时积累(分别为0.75 g/L、占细胞干重的37%和0.6 g/L),然后在72 h时PHB衰减(0.2 g/L)。另一方面,EPS继续生物合成(72 h时为1.1 g/L)。计算了细胞内和细胞外生物聚合物总量中的PHB部分。建议使用不添加铵的蔗糖改良伯克培养基,作为一种能够将碳源用于用褐球固氮菌6B生产细胞内PHB而非EPS的培养基。