Purification and characterization of Escherichia coli guanine-xanthine phosphoribosyltransferase produced by a high efficiency expression plasmid utilizing a lambda PL promoter and CI857 temperature-sensitive repressor.

This publication has 17 references indexed in Scilit:

• Amplification of the uvrA gene product of Escherichia coli to 7% of cellular protein by linkage to the pL promoter of pKC30.
  Proceedings of the National Academy of Sciences, 1982
• High-level synthesis in Escherichia coli of the SV40 small-t antigen under control of the bacteriophage lambda pl promoter
  Gene, 1982
• Plasmid vectors for high-efficiency expression controlled by the promoter of coliphage lambda
  Gene, 1981
• Construction of plasmid cloning vehicles that promote gene expression from the bacteriophage lambda promoter
  Gene, 1979
• [75] Hypoxanthine phosphoribosyltransferase and guanine phosphoribosyltransferase from enteric bacteria
  Published by Elsevier ,1978
• Autoregulation and Function of a Repressor in Bacteriophage Lambda
  Science, 1976
• Xanthine phosphoribosyltransferase from Streptococcus faecalis
  Archives of Biochemistry and Biophysics, 1974
• Guanine phosphoribosyltransferase from Escherichia coli. Specificity and properties
  Biochemistry, 1972
• Inosine and guanine phosphoribosyltransferase in Escherichia coli
  Biochemical and Biophysical Research Communications, 1972
• Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
  Nature, 1970