51878
α-Ketosuberic acid
≥97.0% (HPLC)
别名:
2-Ketosuberic acid, 2-Oxooctanedioic acid
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关于此项目
经验公式（希尔记法）:
C8H12O5
化学文摘社编号:
分子量:
188.18
Beilstein:
1778635
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.25
方案
≥97.0% (HPLC)
表单
solid
储存温度
2-8°C
InChI
1S/C8H12O5/c9-6(8(12)13)4-2-1-3-5-7(10)11/h1-5H2,(H,10,11)(H,12,13)
InChI key
HAGOOZVJLSSXGZ-UHFFFAOYSA-N
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
Yuchen Liu et al.
Environmental microbiology, 14(10), 2632-2644 (2012-05-26)
Studies on sulfur metabolism in archaea have revealed many novel enzymes and pathways and have advanced our understanding on metabolic processes, not only of the archaea, but of biology in general. A variety of dissimilatory sulfur metabolisms, i.e. reactions used
Randy M Drevland et al.
The Journal of biological chemistry, 283(43), 28888-28896 (2008-09-04)
Homoaconitase enzymes catalyze hydrolyase reactions in the alpha-aminoadipate pathway for lysine biosynthesis or the 2-oxosuberate pathway for methanogenic coenzyme B biosynthesis. Despite the homology of this iron-sulfur protein to aconitase, previously studied homoaconitases catalyze only the hydration of cis-homoaconitate to
David E Graham
Methods in enzymology, 494, 301-326 (2011-03-16)
Coenzyme M (CoM) and coenzyme B (CoB) are essential for methane production by the euryarchaea that employ this specialized anaerobic metabolism. Two pathways are known to produce CoM, 2-mercaptoethanesulfonate, and both converge on the 2-oxoacid sulfopyruvate. These cells have recruited
Jeyaraman Jeyakanthan et al.
Biochemistry, 49(12), 2687-2696 (2010-02-23)
The aconitase family of hydro-lyase enzymes includes three classes of proteins that catalyze the isomerization of alpha-hydroxy acids to beta-hydroxy acids. Besides aconitase, isopropylmalate isomerase (IPMI) proteins specifically catalyze the isomerization of alpha,beta-dicarboxylates with hydrophobic gamma-chain groups, and homoaconitase (HACN)
R H White
Biochemistry, 28(24), 9417-9423 (1989-11-28)
The biosynthetic steps involved in the conversion of alpha-ketosuberate to 7-mercaptoheptanoic acid were studied in cell-free extracts of methanogenic bacteria. The pathway was established by measuring the incorporation of stable isotopically labeled precursors into the S-methyl ether methyl ester derivative
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