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Key Documents

Altri documenti

G1763

Sigma-Aldrich

β-Glutamic acid

Sinonimo/i:

3-Aminopentanedioic acid

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About This Item

Formula empirica (notazione di Hill):
C5H9NO4
Numero CAS:
1948-48-7
Peso molecolare:
147.13
Numero MDL:
MFCD00056698
Codice UNSPSC:
12352209
ID PubChem:
24895076
NACRES:
NA.26

Saggio

≥98% (TLC)

Livello qualitativo

100

Forma fisica

powder

tecniche

ligand binding assay: suitable

Colore

white to off-white

Stringa SMILE

NC(CC(O)=O)CC(O)=O

InChI

1S/C5H9NO4/c6-3(1-4(7)8)2-5(9)10/h3H,1-2,6H2,(H,7,8)(H,9,10)
BBJIPMIXTXKYLZ-UHFFFAOYSA-N

Categorie correlate

Azioni biochim/fisiol

β-Glutamic acid (β-Glu) is used as an osmolyte in many archaea. β-Glutamic acid may be used as a substrate to study the specificity and kinetics of archaeal and bacterial glutamine synthetase (GS) enzymes. β-Glutamic acid is used to study primitive mechanisms of polypeptide formation.

Applicazioni

N° Catalogo
Descrizione
Determinazione del prezzo

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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β-Alanine 99%

Sigma-Aldrich

146064

β-Alanine

Acido L-glutammico ReagentPlus®, ≥99% (HPLC)

Sigma-Aldrich

G1251

Acido L-glutammico

Fosfato di potassio ACS reagent, ≥98%

Sigma-Aldrich

P3786

Fosfato di potassio

H McLennan et al.
Neuropharmacology, 21(6), 549-554 (1982-06-01)
Separate receptors are recognized for the excitation of mammalian neurones by (a) L-glutamic and quisqualic acids and (b) N-methyl-D-aspartic (NMDA), and other amino acids which have conformationally restricted molecules. Several other compounds, both agonists and antagonists, have been examined, and
Jean-François Lambert
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 38(3), 211-242 (2008-03-18)
The present paper offers a review of recent (post-1980) work on amino acid adsorption and thermal reactivity on oxide and sulfide minerals. This review is performed in the general frame of evaluating Bernal's hypothesis of prebiotic polymerization in the adsorbed
D E Robertson et al.
Biochimica et biophysica acta, 992(3), 320-326 (1989-09-15)
13C- and 15N-NMR spectroscopy have been used to identify beta-aminoglutaric acid (beta-glutamic) as a major soluble component of the thermophilic, autotrophic marine methanogen Methanococcus thermolithotrophicus. This rare, non-protein amino acid has been recognized as a major dissolved free amino acid
P Robinson et al.
Applied and environmental microbiology, 67(10), 4458-4463 (2001-09-26)
The conversion of beta-glutamate to beta-glutamine by archaeal and bacterial glutamine synthetase (GS) enzymes has been examined. The GS from Methanohalophilus portucalensis (which was partially purified) is capable of catalyzing the amidation of this substrate with a rate sevenfold less
D E Robertson et al.
Applied and environmental microbiology, 56(5), 1504-1508 (1990-05-01)
The unusual compound beta-aminoglutaric acid (beta-glutamate) has been identified by 13C nuclear magnetic resonance spectroscopy in soluble extracts of marine methanogenic bacteria. We examined several methanogen species representing nine genera and found that beta-glutamate occurred in methanococci and two methanogenium
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Chromatograms

application for HPLC

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