Mutational analysis of splicing activities of ribonucleotide reductase α subunit protein from lytic bacteriophage P1201

Curr Microbiol. 2011 Apr;62(4):1282-6. doi: 10.1007/s00284-010-9854-4. Epub 2011 Jan 6.

Abstract

A CP1201 RIR1 intein is found in the ribonucleotide reductase alpha subunit (RNR α subunit) protein of lytic bacteriophage P1201 from Corynebacterium glutamicum NCHU 87078. This intein can be over-expressed and spliced in Escherichia coli NovaBlue cells. Mutations of C539, the N-terminal residue of the C-extein in the CP1201 RIR1 protein, led to the changes of pattern and level of protein-splicing activities. A G392S variant was found to be a temperature-sensitive protein with complete splicing activity at 17 and 28°C but not at 37°C or higher. We also found that the cleavage at the CP1201 RIR1 intein C-terminus of the double mutant G392S/C539G was blocked, but other cleavage activities could be efficiently performed at 17°C. G392S/C539G variant possessed the properties of low-temperature-induced cleavage at the intein N-terminus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Bacteriophages / chemistry
  • Bacteriophages / enzymology*
  • Bacteriophages / genetics
  • Corynebacterium glutamicum / virology
  • Enzyme Stability
  • Inteins
  • Molecular Sequence Data
  • Mutation*
  • Protein Subunits / chemistry
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • RNA Splicing*
  • Ribonucleotide Reductases / chemistry
  • Ribonucleotide Reductases / genetics*
  • Ribonucleotide Reductases / metabolism
  • Viral Proteins / chemistry
  • Viral Proteins / genetics*
  • Viral Proteins / metabolism

Substances

  • Protein Subunits
  • Viral Proteins
  • Ribonucleotide Reductases