Beeley J A, Black P M
Infect Immun. 1977 Jan;15(1):50-8. doi: 10.1128/iai.15.1.50-58.1977.
Streptococcus sanguis 804 (NCTC 10904) was grown ih batch culture at constant pH. and the glucosyltransferase activity of the supernatant was assayed over a 40-h growth period. The optimum pH for enzyme production was 7.0 to 7.2. During growth of the culture, three reproducible phases of enzyme activity were observed. The polysaccharides synthesized during each of these phases were characterized as dextran-like glucans by analysis of acid hydrolysates, gas-liquid chromatography, and a specific aggregation technique. The glucans were studied further by infrared spectroscopy, enzymic degradation, and periodate oxidation. Differences in the proportions of alpha-(1 leads to 3)- and alpha-(1 leads to 6)-linkages were observed. The results suggest that glucan synthesis by S. sanguis involves a multienzyme system.
血链球菌804(NCTC 10904)在恒定pH值下进行分批培养,在40小时的生长周期内测定上清液的葡糖基转移酶活性。酶产生的最适pH值为7.0至7.2。在培养物生长过程中,观察到酶活性的三个可重复阶段。通过酸水解产物分析、气液色谱法和特定聚集技术,将这些阶段中每个阶段合成的多糖表征为类葡聚糖葡聚糖。通过红外光谱、酶降解和高碘酸盐氧化对葡聚糖进行了进一步研究。观察到α-(1→3)-和α-(1→6)-连接比例的差异。结果表明,血链球菌的葡聚糖合成涉及多酶系统。