N-Benzoyl-L-serine
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| Category | Others |
| Catalog number | BBF-05226 |
| CAS | 4877-23-0 |
| Molecular Weight | 209.20 |
| Molecular Formula | C10H11NO4 |
| Purity | >95% by HPLC |
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Specification
| Related CAS | 86808-09-5 (D-configuration) |
| Synonyms | L-Serine, N-benzoyl-; Bz-L-Ser-OH; (S)-2-benzamido-3-hydroxypropanoic acid; N-Bz-serine; benzoyl-L-serine |
| Storage | Store at -20°C |
| IUPAC Name | (2S)-2-benzamido-3-hydroxypropanoic acid |
| Canonical SMILES | C1=CC=C(C=C1)C(=O)NC(CO)C(=O)O |
| InChI | InChI=1S/C10H11NO4/c12-6-8(10(14)15)11-9(13)7-4-2-1-3-5-7/h1-5,8,12H,6H2,(H,11,13)(H,14,15)/t8-/m0/s1 |
| InChI Key | MWCDMTCWMZHVAQ-QMMMGPOBSA-N |
Properties
| Appearance | Needles |
| Melting Point | 148-150°C |
| Solubility | Soluble in Methanol |
Reference Reading
1. Bacteriostatic enterochelin-specific immunoglobulin from normal human serum
D G Moore, R J Yancey, C E Lankford, C F Earhart Infect Immun. 1980 Feb;27(2):418-23. doi: 10.1128/iai.27.2.418-423.1980.
Heat-inactivated normal human serum produces iron-reversible bacteriostasis of a number of microorganisms. This inhibitory effect was abolished by adsorption of serum with ultraviolet-killed cells of species that produce the siderophore enterochelin. Bacteriostasis also was alleviated by adsorption of serum with 2,3-dihydroxy-N-benzoyl-L-serine, a degradation product of enterochelin, bound to the insoluble matrix AH-Sepharose 4B. The adsorption process did not add iron or enterochelin to serum, nor did it remove transferrin. The immunoglobulin fraction from normal human serum was isolated; when added to a defined medium (M199) prepared so as to mimic normal human serum, the immunoglobulin rendered the medium inhibitory to an enterochelin-defective strain of Salmonella typhimurium. Adsorption of this medium with AH-Sepharose 4B-2,3-dihydroxy-N-benzoyl-L-serine removed the inhibition. Our results indicate that enterochelin-specific immunoglobulins exist in normal human serum. These immunoglobulins may act synergistically with transferrin to effect bacteriostasis of enterochelin-producing pathogens.
2. Specific inhibition of Escherichia coli ferrienterochelin uptake by a normal human serum immunoglobulin
D G Moore, C F Earhart Infect Immun. 1981 Feb;31(2):631-5. doi: 10.1128/iai.31.2.631-635.1981.
Normal human serum contains an enterochelin-specific antibody which presumably acts with transferrin to hinder iron assimilation by enterochelin-producing pathogens. This antibody can be isolated from serum by sodium sulfate fractionation or affinity chromatography by employing an enterochelin-derived ligand (2,3-dihydroxy-N-benzoyl-L-serine) attached to aminohexyl Sepharose 4B. In assays of iron uptake by whole cells, the antibody inhibited enterochelin-directed uptake but not that mediated by citrate or ferrichrome. Also, the growth stimulatory effect of enterochelin on an Ent- strain of Escherichia coli was blocked by the immunoglobulin. This antibody has a high affinity for enterochelin; various elution procedures employing high salt concentrations and low pH failed to remove it from affinity columns. Elution with 3 M sodium thiocyanate or 13 mM 2,3-dihydroxybenzoic acid proved successful. Two pieces of evidence indicate the enterochelin-specific antibody is primarily of the immunoglobulin A (IgA) isotype. It could be removed from serum with goat antihuman IgA and was present only in sodium sulfate fractions of serum known to contain IgA.
3. Enzymatic hydrolysis of enterochelin and its iron complex in Escherichia Coli K-12. Properties of enterochelin esterase
K T Greenwood, R K Luke Biochim Biophys Acta. 1978 Jul 7;525(1):209-18. doi: 10.1016/0005-2744(78)90216-4.
Properties of the enzyme which hydrolyses enterochelin (a cyclic trimer of 2,3-dihydroxy-N-benzoyl-L-serine) to 2,3-dihydroxybenzoylserine have been investigated with a view to resolving discrepancies between earlier reports. Enterochelin esterase, previously reported to consists of two components (O'Brien, I.G., Cox, G.B. and Gibson, F. (1971) Biochim. Biophys. Acta 237, 537-549), has been shown to be fully active in the absence of the so-called A component. The hydrolase described previously (Bryce, G.F. and Brot, N. (1972) Biochemistry 11, 1708-1715) as being able to break down enterochelin but not its iron complex, ferric-enterochelin, appears to be identical with the B component of enterochelin esterase. The single component enterochelin esterase corresponding to what was previously described as component B, hydrolyses both enterochelin and ferric-enterochelin. Under the assay conditions used, enterochelin is hydrolysed 2.5 times faster than the complex. Enzymatic activity is inhibited by N-ethylmaleimide and is lost rapidly at 37 degrees C. Activity is stabilized in the presence of ferric-enterochelin, enterochelin, dithiothreitol or certain protein fractions.
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Bio Calculators
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Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
