Cuesta Gabriela, Suarez Norma, Bessio Maria I, Ferreira Fernando, Massaldi Hugo
Departamento de Desarrollo Biotecnológico y Producción, Instituto de Higiene, Universidad de la República, Alfredo Navarro 3051, C.P. 11600 Montevideo, Uruguay.
J Microbiol Methods. 2003 Jan;52(1):69-73. doi: 10.1016/s0167-7012(02)00151-3.
The capsular polysaccharide of Streptococcus pneumoniae, serotype 14, is part of every pneumococcal vaccine presently in the market or under development. A strategy for the quantitative determination of this polysaccharide by the phenol-sulfuric acid method is described. The modality of acid addition is shown to be the critical step for obtaining reproducible test results between different technicians. Raising the incubation temperature above 80 degrees C increased the consistency of the method by more than 60% regardless of the acid addition modality, but at the expense of some loss of sensitivity. Incubation at 110 degrees C was found necessary to obtain reproducible results within 3% for this technique, which was used to follow the enrichment of the polysaccharide during the last steps of purification. A model mixture of the component polysaccharide sugars provided an adequate and economic standard to construct the calibration curve for this assay, with absorbance reading either in the reaction tubes or in a microplate. A similar procedure may be applied to the determination of other bacterial polysaccharides as well.
14型肺炎链球菌的荚膜多糖是目前市场上或正在研发的每种肺炎球菌疫苗的组成部分。本文描述了一种用苯酚-硫酸法对该多糖进行定量测定的策略。结果表明,加酸方式是不同技术人员获得可重复测试结果的关键步骤。无论加酸方式如何,将孵育温度提高到80℃以上可使该方法的一致性提高60%以上,但会损失一些灵敏度。发现110℃孵育对于该技术在3%范围内获得可重复结果是必要的,该技术用于跟踪纯化最后步骤中多糖的富集情况。组成多糖糖的模型混合物提供了一种合适且经济的标准品,用于构建该测定的校准曲线,吸光度可在反应管或微孔板中读取。类似的程序也可应用于其他细菌多糖的测定。