gene amiB, DNA and amino acid sequence determination and analysis, overexpression of the C-terminally His-tagged enzyme in Escherichia coli strain BL21(DE3), subcloning in Escherichia coli strain DH5alpha
gene amiC, recombinant expression of N-terminally His6-tagged enzyme AmiC residues 29-159 fused to GB1 in Escherichia coli strain BL21(DE3), cells are grown in M9 minimal media containing 13C6-glucose and 15NH4Cl as carbon and nitrogen sources, respectively
gene amiC, sequence comparisons, recombinant expression of C-terminally HA-tagged or His6-tagged wild-type and mutant enzymes in Escherichia coli strain DH5alpha
gene cwlB, the gene and upstream gene cwlA form one transcriptional unit, DNA and amino acid sequence determination and analysis, sequence comparison. Transcription of the operon is directed by a promoter, PcwlA, which is located upstream from the cwlA gene and that the transcription start site is a single 5'-end nucleotide residue T located 25 nucleotides upstream from the cwlA translational start codon. The activity of PcwlA is controlled by sigmaK. Subcloning and gene modifications in Escherichia coli strains TG1 and SCS110, recombinant expression of His-tagged enzyme in Escherichia coli strain BL21(DE3)
gene cwlC or RS15875, DNA and amino acid sequence determination and analysis, sequence comparisons, recombinant expression of His-tagged enzyme in Escherichia coli strain BL21(DE3), cwlC is transcribed as a monocistronic unit and its expression is dependent on sporulation sigma factor K
gene IBBPl23_21, DNA and amino acid sequence determination and analysis, recombinant expression of His6-tagged in Escherichia coli strains JM109 and BL21(DE3)
gene lytAB6, DNA and amino acid sequence determination and analysis, phylogenetic analysis, overexpression of the phage enzyme in Escherichia coli strain DH10B
gene lytAHER, DNA and amino acid sequence determination and analysis, phylogenetic analysis, overexpression of the phage enzyme in Escherichia coli strain DH10B
gene pglyrp2, DNA and amino acid sequence determination and analysis, no alternative splice forms, transient expression in COS-7 and HEK-293 cells, expression of wild-type and truncated mutant enzymes in Escherichia coli as inclusion bodies
gene PGRP-SB1, DNA and amino acid sequence determination and analysis, expression of His6-tagged 128 C-terminal residues and of his6-tagged 180 N-terminal residues in Escherichia coli strain XL-1I Blue
gene SA97_036, DNA and amino acid sequence determination and analysis, sequence comparisons and phylogenetic analysis, recombinant expression of N-terminally His-tagged cell wall binding domain CBD fused to GFP in Escherichia coli strain BL21(DE3)
gene sle1, DNA and amino acid sequence determination and analysis, expression of His6-tagged 128 C-terminal residues and of His6-tagged 180 N-terminal residues in Escherichia coli strain XL-1I Blue
synthesis of a gene, codon optimized for Escherichia coli expression, that encodes the catalytic domain of the bacteriophage phiGVE2 amidase and the cell-wall binding (CWB) domain of the endolysin encoded by the genome of phiCP26F, recombinant expression of His-tagged chimeric enzyme PlyGVE2CpCWB in Escherichia coli strain BL21(DE3)
synthesis of a gene, codon optimized for Escherichia coli expression, that encodes the catalytic domain of the bacteriophage phiGVE2 amidase and the cell-wall binding (CWB) domain of the endolysin encoded by the genome of phiCP26F, recombinant expression of His-tagged chimeric enzyme PlyGVE2CpCWB in Escherichia coli strain BL21(DE3)
synthesis of a gene, codon optimized for Escherichia coli expression, that encodes the catalytic domain of the bacteriophage phiGVE2 amidase and the cell-wall binding (CWB) domain of the endolysin encoded by the genome of phiCP26F, recombinant expression of His-tagged chimeric enzyme PlyGVE2CpCWB in Escherichia coli strain BL21(DE3)