Spatafora G, Rohrer K, Barnard D, Michalek S
Department of Biology, Middlebury College, Vermont 05753, USA.
Infect Immun. 1995 Jul;63(7):2556-63. doi: 10.1128/iai.63.7.2556-2563.1995.
We used the streptococcal transposon, Tn916 to identify and isolate mutants of Streptococcus mutans with altered intracellular polysaccharide (IPS) accumulation. We report on the isolation and characterization of S. mutans SMS202, a transposon mutant which accumulated the glycogen-like IPS in excess of wild-type levels. Southern blot analysis confirmed a single Tn916 insertion into the SMS202 chromosome. Moreover, quantitative ultrastructural analysis revealed significantly increased concentrations of IPS in SMS202 relative to those of the wild-type progenitor strain, UA130. The activities of ADPglucose pyrophosphorylase (GlgC) and glycogen synthase (GlgA), enzymes required for the biosynthesis of bacterial IPS, were also elevated in the IPS excess mutant. Furthermore, SMS202 was significantly more cariogenic on the molar surfaces of germ-free rats than the wild type (P < 0.01), thus confirming a central role for IPS in S. mutants-induced caries formation. We propose that the increased cariogenic potential of SMS202 is due to constitutive expression of genes which encode glycogen biosynthesis in this oral pathogen. The coordinate expression of GlgC and GlgA along with the results of ongoing nucleotide sequence analysis and Northern hybridization experiments support an operon-like arrangement for the glg genes of this oral pathogen.
我们使用链球菌转座子Tn916来鉴定和分离变形链球菌中细胞内多糖(IPS)积累发生改变的突变体。我们报告了变形链球菌SMS202的分离和特性,这是一种转座子突变体,其积累的类糖原IPS超过了野生型水平。Southern印迹分析证实Tn916单一插入到SMS202染色体中。此外,定量超微结构分析显示,相对于野生型亲本菌株UA130,SMS202中IPS的浓度显著增加。细菌IPS生物合成所需的酶ADP葡萄糖焦磷酸化酶(GlgC)和糖原合酶(GlgA)的活性在IPS过量突变体中也有所升高。此外,在无菌大鼠的磨牙表面,SMS202的致龋性明显高于野生型(P < 0.01),从而证实了IPS在变形链球菌诱导的龋齿形成中起核心作用。我们认为,SMS202致龋潜力增加是由于该口腔病原体中编码糖原生物合成的基因组成型表达所致。GlgC和GlgA的协同表达以及正在进行的核苷酸序列分析和Northern杂交实验结果支持了该口腔病原体glg基因呈操纵子样排列。