首页> 美国卫生研究院文献>Infection and Immunity >Properties of Streptococcus mutans Grown in a Synthetic Medium: Binding of Glucosyltransferase and In Vitro Adherence and Binding of Dextran/Glucan and Glycoprotein and Agglutination
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Properties of Streptococcus mutans Grown in a Synthetic Medium: Binding of Glucosyltransferase and In Vitro Adherence and Binding of Dextran/Glucan and Glycoprotein and Agglutination

机译:在合成培养基中生长的变形链球菌的特性:葡萄糖基转移酶的结合和体外粘附以及葡聚糖/葡聚糖和糖蛋白的结合和凝集

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摘要

The influence of culture media on various properties of Streptococcus mutans was investigated. Strains of S. mutans (serotypes c, d, f, and g) were grown in a complex medium (Todd-Hewitt broth [THB]) or a synthetic medium (SYN). The SYN cells, in contrast to THB cells, did not bind extracellular glucosyltransferase and did not produce in vitro adherence. Both types of cells possessed constitutive levels of glucosyltransferase. B13 cells grown in SYN plus invertase-treated glucose possessed the same level of constitutive enzyme as THB cells. In contrast to THB cells, the SYN cells of seven serotype strains did not agglutinate upon the addition of high-molecular-weight dextran/glucan. Significant quantities of lower-molecular-weight (2 × 104 or 7 × 104) dextran and B13 glucan were bound by SYN cells. SYN cells agglutinated weakly in anti-glucan serum (titers, 0 to 16), whereas THB cells possessed titers of 32 to 256. Evidence for the existence of a second binding site in agglutination which does not possess a glucan-like polymer has been obtained. B13 cells grown in invertase-treated THB agglutinated to the same degree as normal THB cells. The nature of this site is unknown. SYN cells possess the type-specific polysaccharide antigen. B13 cells did not bind from THB a glycoprotein which reacts with antisera to the A, B, or T blood group antigens or which allows agglutination upon the addition of dextran. The results demonstrate that S. mutans grown in a chemically defined medium possesse markedly different biochemical and biological activities than cells grown in a complex organic medium.
机译:研究了培养基对变形链球菌各种特性的影响。变异链球菌菌株(血清型c,d,f和g)在复合培养基(Todd-Hewitt肉汤[THB])或合成培养基(SYN)中生长。与THB细胞相反,SYN细胞不结合细胞外葡萄糖基转移酶,并且不产生体外粘附。两种类型的细胞都具有组成型水平的葡萄糖基转移酶。在SYN加上转化酶处理的葡萄糖中生长的B13细胞具有与THB细胞相同水平的组成酶。与THB细胞相反,添加高分子量右旋糖酐/葡聚糖后,七个血清型菌株的SYN细胞不会凝集。少量的低分子量(2×10 4 或7×10 4 )右旋糖酐和B13葡聚糖被SYN细胞结合。 SYN细胞在抗葡聚糖血清中微弱凝集(滴度,0至16),而THB细胞的滴度为32至256。已获得在凝集中存在第二个结合位点的证据,该位点不具有葡聚糖样聚合物。 。在用转化酶处理的THB中生长的B13细胞的凝集程度与正常THB细胞相同。该网站的性质未知。 SYN细胞具有类型特异性多糖抗原。 B13细胞未从THB结合糖蛋白,该糖蛋白可与抗血清反应与A,B或T血型抗原,或者在添加右旋糖酐后可凝集。结果表明,在化学成分确定的培养基中生长的变形链球菌与在复杂有机培养基中生长的细胞相比,具有明显不同的生化和生物学活性。

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