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Key Documents

00993

Sigma-Aldrich

L-Xylulose 5-phosphate lithium salt

BioChemika, ≥90% (TLC)

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About This Item

Empirical Formula (Hill Notation):
C5H11O8P · xLi+
CAS Number:
Molecular Weight:
230.11 (free acid basis)
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.32

product line

BioChemika

assay

≥90% (TLC)

SMILES string

OCC([C@H](O)[C@@H](O)COP(O)(O)=O)=O

InChI

1S/C5H11O8P/c6-1-3(7)5(9)4(8)2-13-14(10,11)12/h4-6,8-9H,1-2H2,(H2,10,11,12)/t4-,5-/m0/s1

InChI key

FNZLKVNUWIIPSJ-WHFBIAKZSA-N

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Biochem/physiol Actions

Metabolite of pentose and glucuronate interconversions, ascorbate and aldarate metabolism and microbial metabolism in diverse environments.

Other Notes

To gain a comprehensive understanding of our extensive range of monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Pathway of L-xylose and L-lyxose degradation in Aerobacter aerogenes.
R L ANDERSON et al.
The Journal of biological chemistry, 237, 296-303 (1962-02-01)
J C Sánchez et al.
The Journal of biological chemistry, 269(47), 29665-29669 (1994-11-25)
A silent gene encoding a kinase that specifically phosphorylates L-xylulose was activated and rendered constitutive in mutant cells of Escherichia coli. L-Xylulose kinase was purified to homogeneity and found to be a dimer of two subunits of 55 kDa, highly
Wen Shan Yew et al.
Biochemistry, 43(21), 6427-6437 (2004-05-26)
3-Keto-L-gulonate 6-phosphate decarboxylase (KGPDC) and orotidine 5'-monophosphate decarboxylase (OMPDC) are homologous enzymes that share the (beta/alpha)(8)-fold but catalyze mechanistically distinct reactions [Wise, E., Yew, W. S., Babbitt, P. C., Gerlt, J. A., and Rayment, I. (2002) Biochemistry 41, 3861-3869]. KGPDC
PATHWAYS OF L-ARABITOL AND XYLITOL METABOLISM IN AEROBACTER AEROGENES.
D FOSSITT et al.
The Journal of biological chemistry, 239, 2110-2115 (1964-07-01)
Irina A Rodionova et al.
Environmental microbiology, 15(8), 2254-2266 (2013-02-28)
myo-inositol (MI) is a key sugar alcohol component of various metabolites, e.g. phosphatidylinositol-based phospholipids that are abundant in animal and plant cells. The seven-step pathway of MI degradation was previously characterized in various soil bacteria including Bacillus subtilis. Through a

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