Dibenzothiophene biodesulfurization pathway improvement using diagnostic GFP fusions
- 22 September 2004
- journal article
- research article
- Published by Wiley in Biotechnology & Bioengineering
- Vol. 88 (1) , 94-99
- https://doi.org/10.1002/bit.20220
Abstract
The dibenzothiophene biodesulfurization pathway has shown significant potential for improving the processing of sulfur‐containing fossil fuels. However, the rate of desulfurization is limited by the last enzyme in the pathway, DszB. Genetic constructs designed to produce increased DszB activity were not functional due to low production of DszB, even when using a consensus ribosome binding site. To increase DszB production, the untranslated region 5′ of dszB was mutated using degenerate oligonucleotides and translational fusions with gfp to detect increased translation of dszB. After screening only 96 mutants, several showed increased green fluorescence and two showed increased DszB activity. When cotransformed with the full dszABC operon, the mutant dszB increased the rate of desulfurization ninefold relative to that using the native dszB.Keywords
This publication has 11 references indexed in Scilit:
- Metabolic Engineering of an Aerobic Sulfate Reduction Pathway and Its Application to Precipitation of Cadmium on the Cell SurfaceApplied and Environmental Microbiology, 2000
- Observations of green fluorescent protein as a fusion partner in genetically engineeredEscherichia coli: Monitoring protein expression and solubilityBiotechnology & Bioengineering, 2000
- Biodesulfurization of dibenzothiophene inEscherichia coli is enhanced by expression of aVibrio harveyi oxidoreductase geneBiotechnology & Bioengineering, 2000
- Green Fluorescent Protein as a Real Time Quantitative Reporter of Heterologous Protein ProductionBiotechnology Progress, 1998
- Improved Green Fluorescent Protein by Molecular Evolution Using DNA ShufflingNature Biotechnology, 1996
- Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoterJournal of Bacteriology, 1995
- Characterization of intermediates in the microbial desulfurization of dibenzothiopheneEnergy & Fuels, 1993
- A series of wide-host-range low-copy-number vectors that allow direct screening for recombinantsGene, 1991
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- DNA synthesis during the division cycle of rapidly growing Escherichia coliJournal of Molecular Biology, 1968