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Literature summary for 4.4.1.5 extracted from

  • Lin, F.; Xu, J.; Shi, J.; Li, H.; Li, B.
    Molecular cloning and characterization of a novel glyoxalase I gene TaGly I in wheat (Triticum aestivum L.) (2010), Mol. Biol. Rep., 37, 729-735.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
expressed in tobacco leaves via Agrobacterium tumefaciens infection Triticum aestivum

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
32500
-
calculated from amino acid sequence Triticum aestivum

Organism

Organism UniProt Comment Textmining
Triticum aestivum
-
cultivar Sumai 3
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
methylglyoxal + glutathione
-
Triticum aestivum (R)-S-lactoylglutathione
-
?

Synonyms

Synonyms Comment Organism
glyoxalase I
-
Triticum aestivum
S-D-lactoylglutathione:methylglyoxal lyase
-
Triticum aestivum

Cofactor

Cofactor Comment Organism Structure
glutathione
-
Triticum aestivum

pI Value

Organism Comment pI Value Maximum pI Value
Triticum aestivum calculated from amino acid sequence
-
5.4

Expression

Organism Comment Expression
Triticum aestivum Gly I expression is induced by the inoculation of Fusarium graminearum in wheat spikes, the magnitude of Gly I mRNAs enhances significantly about twofold in 100 mM NaCl, however, with the increase of NaCl concentration to 150 and 500 mM, the Gly I mRNAs decrease to the similar level as control. When treated with ZnCl2, the mRNA level of Gly I in leaves increases gradually with the increase of ZnCl2 concentration up