12271
2-Keto-3-deoxy-D-gluconic acid lithium salt
≥95% (TLC)
동의어(들):
3-Deoxy-D-erythro-2-hexulosonic acid lithium salt, KDG, Lithium 2-keto-3-deoxy-D-gluconate
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C6H10O6 · xLi+
CAS Number:
Molecular Weight:
178.14 (free acid basis)
UNSPSC 코드:
12352204
NACRES:
NA.32
추천 제품
분석
≥95% (TLC)
형태
powder or crystals
저장 온도
−20°C
InChI
1S/C6H10O6/c7-2-5(10)3(8)1-4(9)6(11)12/h3,5,7-8,10H,1-2H2,(H,11,12)/t3-,5+/m0/s1
InChI key
WPAMZTWLKIDIOP-WVZVXSGGSA-N
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생화학적/생리학적 작용
Metabolite in the pentose phosphate pathway, which generates NADPH and pentoses; KDG is an intermediate in the metabolism of glucose and gluconic acid in some pseudomonas strains, of uronic acids in E. coli, and also an important metabolite in the degradation of polygalacturonates in Erwinia chrysanthemi.
포장
Bottomless glass bottle. Contents are inside inserted fused cone.
주의사항
Hygroscopic.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
G Condemine et al.
Journal of bacteriology, 165(3), 937-941 (1986-03-01)
Mutants of Erwinia chrysanthemi impaired in pectin degradation were isolated by chemical and Mu d(Ap lac) insertion mutagenesis. A mutation in the kduD gene coding for 2-keto-3-deoxygluconate oxidoreductase prevented the growth of the bacteria on polygalacturonate as the sole carbon
Carbohydrate metabolism by Pseudomonas fluorescens. III. Purification and properties of a 6-phosphogluconate dehydrase.
R KOVACHEVICH et al.
The Journal of biological chemistry, 213(2), 745-756 (1955-04-01)
Uronic acid metabolism in bacteria. I. Purification and properties of uronic acid isomerase in Escherichia coli.
G ASHWELL et al.
The Journal of biological chemistry, 235, 1559-1565 (1960-06-01)
A new pathway of uronic acid metabolism.
A ASHWELL et al.
Biochimica et biophysica acta, 30(1), 186-187 (1958-10-01)
Glucose and gluconic acid oxidation of Pseudomonas saccharophila.
N ENTNER et al.
The Journal of biological chemistry, 196(2), 853-862 (1952-05-01)
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