Abaas S, Holme T
Scand J Dent Res. 1982 Apr;90(2):109-16. doi: 10.1111/j.1600-0722.1982.tb01532.x.
Streptococcus mitis ATCC 903 grown under glucose-limiting conditions in continuous culture did not aggregate upon incubation in 10 mM phosphate buffer at pH 5--7 unless a metabolizable sugar was added. Aggregation started 45--60 min after the addition of glucose or sucrose whereas slowly metabolized sugars as galactose and lactose required several hours to cause aggregation. Active metabolism of the carbohydrate was a prerequisite for aggregation as indicated by acid formation. Chloramphenicol inhibited the development of aggregating ability in the presence of glucose or sucrose. The addition of a source of nitrogen (peptides and amino acids) enhanced aggregation and shortened the time for development of aggregating ability. No aggregation occurred at at 0 degrees C and the ability to aggregate was markedly delayed at 20 degrees C as compared to 30 degrees C and 37 degrees C. Trypsin treatment of the bacteria abolished aggregation, indicating that surface components of protein or glycoprotein nature contributed to the capacity to aggregate.
在连续培养中于葡萄糖限制条件下生长的缓症链球菌ATCC 903,在pH 5 - 7的10 mM磷酸盐缓冲液中孵育时不会聚集,除非添加可代谢的糖。添加葡萄糖或蔗糖后45 - 60分钟开始聚集,而半乳糖和乳糖等代谢缓慢的糖需要数小时才能引起聚集。如酸形成所示,碳水化合物的活跃代谢是聚集的先决条件。氯霉素在有葡萄糖或蔗糖存在时抑制聚集能力的发展。添加氮源(肽和氨基酸)可增强聚集并缩短聚集能力发展的时间。在0℃时不发生聚集,与30℃和37℃相比,在20℃时聚集能力明显延迟。用胰蛋白酶处理细菌可消除聚集,表明蛋白质或糖蛋白性质的表面成分有助于聚集能力。