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76512

Sigma-Aldrich

D-Ribulose solution

~1 M in H2O, ≥97.0% (HPLC)

Synonyme(s) :

D-erythro-2-Ketopentose solution, D-erythro-2-Pentulose solution, D-Adonose solution, D-Arabinulose solution, D-Araboketose solution, D-Erythropentulose solution

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About This Item

Formule empirique (notation de Hill):
C5H10O5
Numéro CAS:
488-84-6
Poids moléculaire :
150.13
Numéro MDL:
MFCD00004704
Code UNSPSC :
12352204
ID de substance PubChem :
329767154
Nomenclature NACRES :
NA.32

Niveau de qualité

100

Pureté

≥97.0% (HPLC)

Forme

liquid

Concentration

~1 M in H2O

Couleur

colorless

Température de stockage

2-8°C

Chaîne SMILES 

OCC1(O)OC[C@@H](O)[C@H]1O

InChI

1S/C5H10O5/c6-2-5(9)4(8)3(7)1-10-5/h3-4,6-9H,1-2H2/t3-,4-,5?/m1/s1

Clé InChI

LQXVFWRQNMEDEE-ZZKAVYKESA-N

Actions biochimiques/physiologiques

D-Ribulose is a metabolite in pentose and glucuronate interconversions. It plays a role in the D-arabitol production from U. fabae. Ribulose is a rare aldopentose that might show antitumoral and antiviral activities. It acts as a substrate for nicotinamide adenine dinucleotide phosphate (NADP+)-dependent D-arabitol dehydrogenase (ARD1p) enzyme and D-tagatose-3-epimerase from Rhodobacter sphaeroides. Its monophosphate D-ribulose 5-phosphate is an intermediate in the pentose phosphate pathway of glycolysis. D-Ribulose may be found in plants like algae, sugar beet leaves, and barley seed leaves.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Autres remarques

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

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Enzyme and microbial technology, 131, 109427-109427 (2019-10-17)
d-Ribulose and l-fuculose are potentially valuable rare sugars useful for anticancer and antiviral drugs in the agriculture and medicine industries. These rare sugars are usually produced by chemical methods, which are generally expensive, complicated and do not meet the increasing
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Applied microbiology and biotechnology, 87(6), 1993-1999 (2010-05-25)
Recombinant Escherichia coli harboring the L: -arabinose isomerase (BLAI) from Bacillus licheniformis was used as a biocatalyst to produce L: -ribulose in the presence of borate. Effects of substrate concentration, the borate to L: -arabinose ratio, pH, and temperature on
Chakkiath Paul Antony et al.
International journal of systematic and evolutionary microbiology, 62(Pt 7), 1613-1618 (2011-09-06)
A moderately haloalkaliphilic methylotrophic bacterium possessing the ribulose monophosphate pathway for carbon assimilation, designated MPL(T), was isolated from Lonar Lake sediment microcosms that were oxidizing methane for two weeks. The isolate utilized methanol and was an aerobic, Gram-negative, asporogenous, motile
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Preparative biochemistry & biotechnology, 40(1), 65-75 (2009-12-22)
Recombinant Escherichia coli whole cells harboring Bacillus licheniformis L-arabinose isomerase (BLAI) were harvested to prepare alginate-immobilized biocatalysts. The operational conditions for immobilization were optimized according to relative activity and the cell leakage of the immobilized cell. The optimal conditions are
Kosei Takeda et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 64(Pt 10), 945-948 (2008-10-22)
D-Arabinose isomerase catalyzes the isomerization of D-arabinose to D-ribulose. Bacillus pallidus D-arabinose isomerase has broad substrate specificity and can catalyze the isomerization of D-arabinose, L-fucose, L-xylose, L-galactose and D-altrose. Recombinant B. pallidus D-arabinose isomerase was overexpressed, purified and crystallized. A
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