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Chemical Compound Review:

D-Erythrose 2,3,4-trihydroxybutanal

Synonyms: CHEMBL25834, AG-H-92797, ACMC-20albn, CTK2G8859, AC1L2R37, ...

Nishimura, K. et al.

Nishimura, Harada, Arita, Watanabe, Iwabuki, Terada, Naganuma, Uzuka,

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High impact information on L-Erythrose

The research of the substrate specificity in the reductive reaction demonstrated that L-erythrulose and dihydroxyacetone were better substrates, that D-acetoin was inactive and L-erythrose (aldose) was slightly active [1].

References

Identification of enzyme responsible for erythritol utilization and reaction product in yeast Lipomyces starkeyi. Nishimura, K., Harada, T., Arita, Y., Watanabe, H., Iwabuki, H., Terada, A., Naganuma, T., Uzuka, Y. J. Biosci. Bioeng. (2006) [Pubmed]

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