1987
DOI: 10.1111/j.1749-6632.1987.tb45691.x
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Characterization and Cloning of Glucose Isomerase from Streptomyces violaceoniger

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Cited by 6 publications
(4 citation statements)
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“…For cloning, DNA from S. violaceoniger was extracted and ligated with plasmid pUT 206. Enzyme deficient strains were transformed with the plasmid and positive glucose isomerase transformants selected (Viot et al, 1987). Using Saccharomyces cerevisiae expression vectors, the E. coli isomerase gene has been introduced into S. cerevisiae.…”
Section: Genetics and Regulationmentioning
confidence: 99%
“…For cloning, DNA from S. violaceoniger was extracted and ligated with plasmid pUT 206. Enzyme deficient strains were transformed with the plasmid and positive glucose isomerase transformants selected (Viot et al, 1987). Using Saccharomyces cerevisiae expression vectors, the E. coli isomerase gene has been introduced into S. cerevisiae.…”
Section: Genetics and Regulationmentioning
confidence: 99%
“…Viot et al [40] reported that the Xyl isomerase of S. violuceoniger might contain sulfhydryl groups essential to activity probably located at the metal-binding site. Sulfhydryl ligands at the metal-binding sites in the S. rubiginosus enzyme, however, can be excluded, since sulfur -Co2 + charge-transfer transitions, which should occur in the region between 230-400 nm [41], could not be observed in the visible, CD and MCD spectra.…”
Section: Discussionmentioning
confidence: 99%
“…Enzyme deficient strains were transformed with the plasmid and positive glucose isomerase transformants selected (Viot et al, 1987). For cloning, DNA from S. violaceoniger was extracted and ligated with plasmid pUT 206.…”
Section: Genetics and Regulationmentioning
confidence: 99%