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7OSO

The crystal structure of Erwinia tasmaniensis levansucrase in complex with (S)-1,2,4-butanentriol

Summary for 7OSO
Entry DOI10.2210/pdb7oso/pdb
DescriptorLevansucrase (Beta-D-fructofuranosyl transferase), ZINC ION, (2~{S})-butane-1,2,4-triol, ... (4 entities in total)
Functional Keywordsfructosyltransferase, levan, fos, transfructosylation, fructo-oligosaccharides, oligofructans, transferase
Biological sourceErwinia tasmaniensis (strain DSM 17950 / CIP 109463 / Et1/99)
Total number of polymer chains1
Total formula weight46441.58
Authors
Polsinelli, I.,Salomone-Stagni, M.,Benini, S. (deposition date: 2021-06-09, release date: 2022-06-22, Last modification date: 2024-02-07)
Primary citationPolsinelli, I.,Salomone-Stagni, M.,Benini, S.
Erwinia tasmaniensis levansucrase shows enantiomer selection for (S)-1,2,4-butanetriol.
Acta Crystallogr.,Sect.F, 78:289-296, 2022
Cited by
PubMed Abstract: Levansucrases are biotechnologically interesting fructosyltransferases due to their potential use in the enzymatic or chemo-enzymatic synthesis of glycosides of non-natural substrates relevant to pharmaceutical applications. The structure of Erwinia tasmaniensis levansucrase in complex with (S)-1,2,4-butanetriol and its biochemical characterization suggests the possible application of short aliphatic moieties containing polyols with defined stereocentres in fructosylation biotechnology. The structural information revealed that (S)-1,2,4-butanetriol mimics the natural substrate. The preference of the protein towards a specific 1,2,4-butanetriol enantiomer was assessed using microscale thermophoresis binding assays. Furthermore, the results obtained and the structural comparison of levansucrases and inulosucrases suggest that the fructose binding modes could differ in fructosyltransferases from Gram-positive and Gram-negative bacteria.
PubMed: 35924596
DOI: 10.1107/S2053230X2200680X
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.4 Å)
Structure validation

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