Zhou R, Chen S, Recsei P
Public Health Research Institute, New York, New York 10016.
Anal Biochem. 1988 May 15;171(1):141-4. doi: 10.1016/0003-2697(88)90134-0.
We describe a method for determination of lysostaphin activity using Remazol Brilliant Blue R (RBB)-dyed staphylococcal cells or RBB-dyed staphylococcal peptidoglycan as substrate. The dyed substrates are easy to prepare and are stable for at least 6 months. Soluble hydrolytic products released by lysostaphin are measured spectrophotometrically at 595 nm after the insoluble substrate is removed by filtration or centrifugation. The dye release assay is more sensitive and more accurate than the previously described turbidimetric assay.
我们描述了一种使用瑞玛唑仑亮蓝R(RBB)染色的葡萄球菌细胞或RBB染色的葡萄球菌肽聚糖作为底物来测定溶葡萄球菌酶活性的方法。染色的底物易于制备且至少6个月稳定。在通过过滤或离心除去不溶性底物后,通过分光光度法在595nm处测量溶葡萄球菌酶释放的可溶性水解产物。与先前描述的比浊法相比,染料释放测定法更灵敏、更准确。