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120124-51-8

120124-51-8 Structure

120124-51-8 Structure
IdentificationBack Directory
[Name]

chrysobactin
[CAS]

120124-51-8
[Synonyms]

chrysobactin
L-Serine, N2-(2,3-dihydroxybenzoyl)-D-lysyl-
[Molecular Formula]

C16H23N3O7
[MOL File]

120124-51-8.mol
[Molecular Weight]

369.37
Hazard InformationBack Directory
[Description]

Chrysobactin is isolated from Erwinia chrysanthemi. Chrysobactin has siderophore activity.
[Uses]

Chrysobactin is a compound isolated from the plant pathogenic bacterium Erwinia chrysanthemi. Chrysobactin has siderophore activity[1].
[Definition]

ChEBI: Chrysobactin is a catechol-type siderophore with a structure of D-lysyl-L-serine substituted on N(2) of the lysyl residue by a 2,3-dihydroxybenzoyl group. It is produced by the Gram-negative bacillus Dickeya dadantii (previously known as Erwinia chrysanthem). Only the catecholate hydroxyl groups participate in metal coordination, so chrysobactin cannot provide full 1:1 coordination of Fe(III); at neutral pH and concentrations of about 0.1 mM, ferric chrysobactin exists as a mixture of bis and tris complexes. It has a role as a siderophore and a bacterial metabolite. It is a member of catechols, a dipeptide, a monocarboxylic acid, a primary alcohol and a primary amino compound.
[References]

[1] Persmark M, et al. Isolation, characterization, and synthesis of chrysobactin, a compound with siderophore activity from Erwinia chrysanthemi. J Biol Chem. 1989 Feb 25;264(6):3187-93. PMID:2914949
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