Nucleotide sequence of Escherichia coli katE, which encodes catalase HPII
Open Access
- 1 January 1991
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 173 (2) , 514-520
- https://doi.org/10.1128/jb.173.2.514-520.1991
Abstract
A 3,466-bp nucleotide sequence containing the katE gene of Escherichia coli has been determined. An open reading frame of 2,259 bp was found and was preceded by a potential ribosome-binding site. The predicted N-terminal sequence agreed with the sequence determined by direct amino acid sequencing, and the predicted direction of transcription was confirmed by expression of the gene cloned in both directions behind a T7 promoter. The start site of transcription was determined to be 127 bp upstream from the start of the open reading frame, and a potential RNA polymerase-binding site similar to a sequence preceding the xthA gene, which is also controlled by the KatF protein, was identified. The predicted sequence of the 753-amino-acid protein was compared with known sequences of other catalases, revealing significant similarity to the shorter catalases, including the residues in the putative active site and residues involved in heme binding.Keywords
This publication has 38 references indexed in Scilit:
- Structure of beef liver catalasePublished by Elsevier ,2005
- Crystallization and preliminary X-ray diffraction analysis of catalase HPII from Escherichia coliJournal of Molecular Biology, 1990
- Proposed structure for the prosthetic group of the catalase HPII from Escherichia coliJournal of the American Chemical Society, 1989
- Catalase gene of the yeast Candida tropicalisEuropean Journal of Biochemistry, 1987
- Nucleotide sequence of the Saccharomyces cerevisiae CTT1 gene and deduced amino‐acid sequence of yeast catalase TEuropean Journal of Biochemistry, 1986
- Purification and characterization of catalase HPII from Escherichia coli K12Biochemistry and Cell Biology, 1986
- The active center of catalaseJournal of Molecular Biology, 1985
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Phosphate-controlled gene expression in Escherichia coli K12 using Mudl-directed lacZ fusionsJournal of Molecular Biology, 1982
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970