Bienkowska-Szewczyk K, Lipinska B, Taylor A
Mol Gen Genet. 1981;184(1):111-4. doi: 10.1007/BF00271205.
The radioactively labeled proteins synthesised in Escherichia coli minicells infected by bacteriophage lambda R and lambda R+ were compared by polyacrylamide gel electrophoresis. lambda R mutants, which have lost the ability to lyse host cells, lack a polypeptide of molecular weight 17.5 KD corresponding to the molecular weight of murein transglycosylase - a bacteriolytic enzyme from lambda lysates which we have described previously. It has been shown by direct comparison using radio-labeled enzyme that transglycosylase comigrates with the R gene product. The enzyme was undetectable in induced cultures of E. coli W3350 su degrees (lambda cI857 Ram 5) and C600 (lambda cI857 acR301), while it was present in a lambda Rz mutant lysate. We conclude that the transglycosylase is the R gene product.
通过聚丙烯酰胺凝胶电泳比较了在被噬菌体λR和λR +感染的大肠杆菌微小细胞中合成的放射性标记蛋白质。λR突变体已失去裂解宿主细胞的能力,缺乏一种分子量为17.5 KD的多肽,该多肽对应于胞壁质转糖基酶的分子量,胞壁质转糖基酶是一种来自λ裂解物的溶菌酶,我们之前已经描述过。通过使用放射性标记酶的直接比较表明,转糖基酶与R基因产物共迁移。在大肠杆菌W3350 su度(λcI857 Ram 5)和C600(λcI857 acR301)的诱导培养物中未检测到该酶,而在λRz突变体裂解物中存在该酶。我们得出结论,转糖基酶是R基因产物。