5-Benzyl L-glutamate
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5-Benzyl L-glutamate

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Category
L-Amino Acids
Catalog number
BAT-004130
CAS number
1676-73-9
Molecular Formula
C12H15NO4
Molecular Weight
237.30
5-Benzyl L-glutamate
IUPAC Name
(2S)-2-amino-5-oxo-5-phenylmethoxypentanoic acid
Synonyms
L-Glu(OBzl)-OH; L-Glutamic acid 5-benzyl ester; gamma-Benzyl L-glutamate; L-Glutamic acid 5-benzyl ester; γ-Benzyl L-glutamate; H-Glu(OBzl)-OH; 5-Benzyl L-GlutaMate
Appearance
White to off-white powder
Purity
≥ 99.7% (Chiral HPLC)
Density
1.245 g/cm3
Melting Point
155-161 °C
Boiling Point
379.8 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H15NO4/c13-10(12(15)16)6-7-11(14)17-8-9-4-2-1-3-5-9/h1-5,10H,6-8,13H2,(H,15,16)/t10-/m0/s1
InChI Key
BGGHCRNCRWQABU-JTQLQIEISA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)CCC(C(=O)O)N
1.Recent advances in amino acid production by microbial cells.
Hirasawa T1, Shimizu H2. Curr Opin Biotechnol. 2016 May 2;42:133-146. doi: 10.1016/j.copbio.2016.04.017. [Epub ahead of print]
Amino acids have been utilized for the production of foods, animal feeds and pharmaceuticals. After the discovery of the glutamic acid-producing bacterium Corynebacterium glutamicum by Japanese researchers, the production of amino acids, which are primary metabolites, has been achieved using various microbial cells as hosts. Recently, metabolic engineering studies on the rational design of amino acid-producing microbial cells have been successfully conducted. Moreover, the technology of systems biology has been applied to metabolic engineering for the creation of amino acid-producing microbial cells. Currently, new technologies including synthetic biology, single-cell analysis, and evolutionary engineering have been utilized to create amino acid-producing microbial cells. In addition, useful compounds from amino acids have been produced by microbial cells. Here, current researches into the metabolic engineering of microbial cells toward production of amino acids and amino acid-related compounds are reviewed.
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