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Literature summary for 3.1.1.110 extracted from

  • Toivari, M.; Nygard, Y.; Kumpula, E.; Vehkomaeki, M.; Bencina, M.; Valkonen, M.; Maaheimo, H.; Andberg, M.; Koivula, A.; Ruohonen, L.; Penttilae, M.; Wiebe, M.
    Metabolic engineering of Saccharomyces cerevisiae for bioconversion of D-xylose to D-xylonate (2012), Metab. Eng., 14, 427-436 .
    View publication on PubMed

Application

Application Comment Organism
synthesis when engineering Saccharomyces cerevisiae for production of D-xylonate from D-xylose, a strain expressing the D-xylonolactone lactonase xylC along with D-xylose dehydrogenase xylB excretes more D-xylonate earlier during the cultivation, both at pH 5.5 and at pH3, than the strains lacking the lactonase. In Sacchaormyces cerevisiae, the linear form may be more toxic than the lactone form and a more gradual hydrolysis of the lactone form may be advantageous to the cell Caulobacter vibrioides

Organism

Organism UniProt Comment Textmining
Caulobacter vibrioides Q9A9Z1
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Caulobacter vibrioides ATCC 19089 Q9A9Z1
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Synonyms

Synonyms Comment Organism
CC_0820
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Caulobacter vibrioides
XylC
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Caulobacter vibrioides