Leong D, Coleman K D, Murphy J R
J Biol Chem. 1983 Dec 25;258(24):15016-20.
The diphtheria toxin fragment A-related polypeptide encoded by the recombinant plasmid pDT201 (Leong, D., Coleman, K. D., and Murphy, J. R. (1983) Science 220, 515-517) and expressed in Escherichia coli K12 was found to have an electrophoretic mobility in sodium dodecyl sulfate-polyacrylamide gels corresponding to 28,500 daltons. Immunoprecipitation experiments revealed that the mature form of the fragment A-related polypeptide was exported to the periplasmic compartment of E. coli K12 harboring plasmid pDT201. The polypeptide was sensitive to trypsin "nicking." Following treatment an Mr = 24,000 fragment was released which co-electrophoresed with fragment A of diphtheria toxin. The precursor form (Mr = 31,000) of the fragment A-related polypeptide was found to accumulate in the cytoplasmic fraction of the temperature-sensitive secretion-defective strain of E. coli K12 under nonpermissive conditions. We further demonstrate that a 263-base pair HaeIII fragment of pDT201 which carries the putative diphtheria tox promoter has promoter activity in E. coli K12.
重组质粒pDT201(梁,D.,科尔曼,K.D.,和墨菲,J.R.(1983年)《科学》220,515 - 517)编码并在大肠杆菌K12中表达的白喉毒素片段A相关多肽,在十二烷基硫酸钠 - 聚丙烯酰胺凝胶中的电泳迁移率对应于28,500道尔顿。免疫沉淀实验表明,片段A相关多肽的成熟形式被转运至携带质粒pDT201的大肠杆菌K12的周质区室。该多肽对胰蛋白酶“切割”敏感。处理后释放出一个Mr = 24,000的片段,其与白喉毒素的片段A共电泳。在非允许条件下,片段A相关多肽的前体形式(Mr = 31,000)在大肠杆菌K12的温度敏感型分泌缺陷菌株的细胞质部分中积累。我们进一步证明,携带推定的白喉毒素启动子的pDT201的一个263碱基对的HaeIII片段在大肠杆菌K12中具有启动子活性。