Buchanan M J, Snell W J
Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas 75235.
Exp Cell Res. 1988 Nov;179(1):181-93. doi: 10.1016/0014-4827(88)90357-6.
New methods have been developed for the purification and characterization of the cell wall degrading enzyme, lysin, which is released into the medium during the mating reaction of the biflagellated alga Chlamydomonas reinhardtii. A quantitative spectrophotometric assay that detects the number of cells losing walls was used to devise a procedure for the 60-fold purification of lysin from the medium of mating gametes with a 30% yield of activity. Molecular sieve and ion exchange chromatography in combination with SDS-PAGE showed that lysin was a single polypeptide with an Mr of 60,000. High-performance liquid chromatography and sucrose density gradient centrifugation of lysin activity were used to obtain an estimate of 66,000 D for the nondenatured molecular weight of lysin, indicating that lysin behaves as a monomer.
已经开发出了新方法,用于纯化和鉴定细胞壁降解酶溶素。在双鞭毛藻类莱茵衣藻的交配反应过程中,溶素会释放到培养基中。一种定量分光光度测定法可检测失去细胞壁的细胞数量,利用该方法设计了一种从交配配子培养基中纯化溶素的程序,纯化倍数达60倍,活性回收率为30%。分子筛和离子交换色谱结合SDS-PAGE分析表明,溶素是一种单一多肽,相对分子质量为60,000。通过高效液相色谱和溶素活性的蔗糖密度梯度离心法,估计溶素的非变性分子量为66,000 D,这表明溶素表现为单体。