Literature summary for 2.4.1.140 extracted from

Joucla, G.; Pizzut, S.; Monsan, P.; Remaud-Simeon, M.
Construction of a fully active truncated alternansucrase partially deleted of its carboxy-terminal domain (2006), FEBS Lett., 580, 763-768.

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Cloned(Commentary)

Cloned (Comment)	Organism
recombinant expression of the large alternansucrase (2057 amino acids) is hindered in Escherichia coli due to poor enzyme solubility and protein degradation. A truncated variant deleted of the APY repeats but harboring four C-terminal CW-like repeats display a high specific activity and the same specificity of product synthesis as the native enzyme. It is more soluble and suffers less degradation than full length alternansucrase	Leuconostoc mesenteroides

Cloned (Comment)

Organism

recombinant expression of the large alternansucrase (2057 amino acids) is hindered in Escherichia coli due to poor enzyme solubility and protein degradation. A truncated variant deleted of the APY repeats but harboring four C-terminal CW-like repeats display a high specific activity and the same specificity of product synthesis as the native enzyme. It is more soluble and suffers less degradation than full length alternansucrase

Leuconostoc mesenteroides

Organism

Organism	UniProt	Comment	Textmining
Leuconostoc mesenteroides	Q9RE05	-	-

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Release 2023.1 (January 2023)