Stein D S, Libertin C R
Department of Medicine, Loyola University Stritch School of Medicine, Maywood, Illinois 60153.
J Clin Microbiol. 1989 Jan;27(1):207-9. doi: 10.1128/jcm.27.1.207-209.1989.
We demonstrated by spectral analysis a method to enzymatically cleave the chromophore precursor from nutritionally deficient streptococcal cell walls by treatment with lysozyme. The peak absorbances without and with lysozyme pretreatment were 511.4 +/- 2.02 nm and 513.1 +/- 0.69 nm, respectively. Extraction yields varied among strains and were found to be growth phase dependent. A secondary peak of absorbance (mean of 477 nm) was found in only five of eight strains. The chromophore at a neutral pH undergoes a reaction with phenol consistent with that of a furan, indicating its carbohydrate composition.
我们通过光谱分析证明了一种方法,即通过用溶菌酶处理,从营养缺陷型链球菌细胞壁上酶解发色团前体。未经溶菌酶预处理和经溶菌酶预处理后的峰值吸光度分别为511.4±2.02纳米和513.1±0.69纳米。提取率因菌株而异,并且发现其依赖于生长阶段。在八个菌株中,只有五个菌株出现了吸光度的二级峰(平均477纳米)。发色团在中性pH下与苯酚发生的反应与呋喃的反应一致,表明其碳水化合物组成。