Host Vector System with the PR, Promoter of Phage Lambda

作者: N. I. Matvienko , I. N. Troyanovskaya , L. A. Zheleznaya , O. B. Yarchuk

DOI: 10.1007/978-94-011-6565-5_17

关键词: Cell biologyTranscription (biology)Lambda phagePromoterAntiterminationChemistryGeneCosmidBacteriophageRepressor

摘要: The early promoters of bacteriophage lambda (PL and PR) are widely used to regulate expression inserted genes. Despite the fact that PR, promoter is strongest transcription start site phage (1), vector molecules with this for foreign genes have not yet been constructed. This may be accounted by complex two-step process regulation from PR. promoter. Firstly inactivation repressor must occur allow PL N gene acts as a product antiterminator permitting extension into Q, whose protein product, in its turn, activates late lambda. It has proposed activation results antitermination 6S RNA, transcript permanently synthesized (1). Therefore order create host-vector system it necessary defective pro-phage includes cI, deletion

参考文章(7)
M. Castellazzi, P. Brachet, H. Eisen, Isolation and characterization of deletions in bacteriophage lambda residing as prophage in E. coli K 12. Molecular Genetics and Genomics. ,vol. 117, pp. 211- 218 ,(1972) , 10.1007/BF00271648
Alfred Day Hershey, The Bacteriophage Lambda. ,(1971)
Jeffrey H Miller, Experiments in molecular genetics ,(1972)
Hans-Ulrich Bernard, Erik Remaut, M. Vickers Hershfield, Hirendra K. Das, Donald R. Helinski, Charles Yanofsky, Naomi Franklin, Construction of plasmid cloning vehicles that promote gene expression from the bacteriophage lambda pL promoter. Gene. ,vol. 5, pp. 59- 76 ,(1979) , 10.1016/0378-1119(79)90092-1
C. M. Joyce, N. D. Grindley, Construction of a plasmid that overproduces the large proteolytic fragment (Klenow fragment) of DNA polymerase I of Escherichia coli. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 80, pp. 1830- 1834 ,(1983) , 10.1073/PNAS.80.7.1830