Comparative Production of Green Fluorescent Protein Under Co-expression of Bacterial Hemoglobin in Escherichia coli W3110 Using Different Culture Scales |
Bassapa Johnvesly
(Department of Chemical Engineering, Pohang University of Science and Technology)
Kang, Dong-Gyun (Department of Chemical Engineering, Pohang University of Science and Technology, Division of Molecular and Life Sciences, Pohang University of Science and Technolog) Park, Suk-Soon (Department of Environmental Engineering, Semyung University) Kim, Ji-Hyun (Department of Chemical Engineering, Dongguk University) Cha, Hyung-Joon (Department of Chemical Engineering, Pohang University of Science and Technology, Division of Molecular and Life Sciences, Pohang University of Science and Technology) |
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Promoter region of the nar operon of Escherichia coli: nucleotide sequence and transcription initiation signals
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DOI |
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Intracellular expression of Vitreoscilla hemoglobin (VHb) enhances total protein secretion and improves the production of α-amylase and neutral protease in bacillus subtilis
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Production of α-amylase in fed-batch cultures of <TEX>$vgb^+$</TEX> and <TEX>$vgb^+$</TEX> recombinant Escherichia coli: Some observations
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4 |
Comparison of green fluorescent protein expression in two industrial Escherichia coli strains, BL21 and W3110, under co-expression of bacterial hemoglobin
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5 |
Enhanced detoxification of organophosphates using recombinant Escherichia coli with co-expression of organophosphorus hydrolase and bacterial hemoglobin
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6 |
Co-expression of bacterial hemoglobin overrides high glucose-induced repression of heterologous protein expression in Escherichia coli W3110
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Whole cell enzyme microencapsulation of Escherichia coli with oxygen-dependent inducible nar promoter
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DOI ScienceOn |
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9 |
The Vitreoscilla hemoglobin gene: molecular cloning, nucleotide sequence and genetic expression in Escherichia coli
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10 |
Insect larval expression process is optimized by generating fusions with green fluorescent protein
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11 |
Observations of green fluorescent protein as a fusion partner in genetically engineered Escherichia coli: Monitoring protein expression and solubility
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12 |
In vitro combinatorial mutagenesis of the 65th and 222nd positions of the green fluorescent protein of Aequarea victoria
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13 |
Construction of glomerular epithelial cells expressing both immune tolerance and GFP genes and application to cell therapy by cell transplantation
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14 |
Study of Vitreoscilla hemoglobin (vhb) gene expression and promoter activity in E. coli through transcriptional fusion
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