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アッセイ
≥90% (TLC)
フォーム
powder
光学活性
[α]/D +78±3°, c = 2 in H2O
適合性
corresponds for H-NMR
保管温度
2-8°C
SMILES記法
O[C@H]([C@@H]([C@@H](O)C)O1)[C@H](O)C1=O
InChI
1S/C6H10O5/c1-2(7)5-3(8)4(9)6(10)11-5/h2-5,7-9H,1H3/t2-,3?,4+,5+/m0/s1
InChI Key
VASLEPDZAKCNJX-MEFNJWCVSA-N
生物化学的／生理学的作用
Metabolite in the fructose and mannose metabolism
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
最新バージョンのいずれかを選択してください：
H S Bleeg et al.
European journal of biochemistry, 127(2), 391-396 (1982-10-01)
An enzyme from Saccharomyces cerevisiae which catalyzes the reaction: L-galactonolactone + O2 leads to L-ascorbate + H2O2 has been purified 466-fold from the mitochondrial fraction of a yeast homogenate. The enzyme has several properties that are different from the L-galactonolactone
Isolation of diphosphopyridine nucleotide-dependent L-fucose dehydrogenase from pork liver.
H Schachter et al.
The Journal of biological chemistry, 244(17), 4785-4792 (1969-09-10)
Merlin Eric Hobbs et al.
Biochemistry, 53(28), 4661-4670 (2014-06-26)
A previously unknown metabolic pathway for the utilization of l-galactose was discovered in a prevalent gut bacterium, Bacteroides vulgatus. The new pathway consists of three previously uncharacterized enzymes that were found to be responsible for the conversion of l-galactose to
Anikó Várnai et al.
Applied and environmental microbiology (2018-04-01)
Fungi secrete a set of glycoside hydrolases and oxidoreductases, including lytic polysaccharide monooxygenases (LPMOs), for the degradation of plant polysaccharides. LPMOs catalyze the oxidative cleavage of glycosidic bonds after activation by an external electron donor. So far, only flavin-dependent oxidoreductases
Merlin Eric Hobbs et al.
Biochemistry, 52(1), 239-253 (2012-12-12)
A member of the amidohydrolase superfamily, BmulJ_04915 from Burkholderia multivorans, of unknown function was determined to hydrolyze a series of sugar lactones: L-fucono-1,4-lactone, D-arabino-1,4-lactone, L-xylono-1,4-lactone, D-lyxono-1,4-lactone, and L-galactono-1,4-lactone. The highest activity was shown for L-fucono-1,4-lactone with a k(cat) value of
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