Nitrogen Fixation and Soybean Genetics Laboratory and Horticultural Crops Quality Laboratory, Agricultural Research Service, U.S. Department of Agriculture, Beltsville, Maryland 20705.
Appl Environ Microbiol. 1990 Jun;56(6):1518-22. doi: 10.1128/aem.56.6.1518-1522.1990.
Bradyrhizobium japonicum USDA 110 synthesized both extracellular and periplasmic polysaccharides when grown on mannitol minimal medium. The extracellular polysaccharides were separated into a high-molecular-weight acidic capsular extracellular polysaccharide fraction (90% of total hexose) and three lower-molecular-weight glucan fractions by liquid chromatography. Periplasmic glucans, extracted from washed cells with 1% trichloroacetic acid, gave a similar pattern on liquid chromatography. Linkage analysis of the major periplasmic glucan fractions demonstrated mainly 6-linked glucose (63 to 68%), along with some 3,6- (8 to 18%), 3- (9 to 11%), and terminal (7 to 8%) linkages. The glucose residues were beta-linked as shown by H-nuclear magnetic resonance analysis. Glucan synthesis by B. japonicum cells grown on mannitol medium with 0 to 350 mM fructose as osmolyte was measured. Fructose at 150 mM or higher inhibited synthesis of periplasmic and extracellular 3- and 6-linked glucans but had no effect on the synthesis of capsular acidic extracellular polysaccharides.
当在甘露醇最小培养基上生长时,大豆慢生根瘤菌 USDA110 合成了胞外和周质多糖。胞外多糖通过液相色谱法分离成高分子量酸性荚膜胞外多糖级分(总己糖的 90%)和三种低分子量葡聚糖级分。用 1%三氯乙酸从洗涤细胞中提取的周质葡聚糖在液相色谱上也呈现出相似的图谱。主要周质葡聚糖级分的连接分析表明,主要是 6 连接的葡萄糖(63%至 68%),还有一些 3,6-(8%至 18%)、3-(9%至 11%)和末端(7%至 8%)连接。如 H-核磁共振分析所示,葡萄糖残基为β连接。用甘露醇培养基培养大豆慢生根瘤菌,培养基中果糖的浓度为 0 至 350mM,以此来测量葡聚糖的合成。150mM 或更高浓度的果糖抑制了周质和胞外 3 连接和 6 连接的葡聚糖的合成,但对酸性荚膜胞外多糖的合成没有影响。