Improved one-pot multienzyme (OPME) systems for synthesizing UDP-uronic acids and glucuronides

Arabidopsis thaliana glucuronokinase (AtGlcAK) was cloned and shown to be able to use various uronic acids as substrates to produce the corresponding uronic acid-1-phosphates. AtGlcAK or Bifidobacterium infantis galactokinase (BiGalK) was used with a UDP-sugar pyrophosphorylase, an inorganic pyropho...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2015-03, Vol.51 (22), p.4595-4598
Hauptverfasser: Muthana, Musleh M, Qu, Jingyao, Xue, Mengyang, Klyuchnik, Timofey, Siu, Alex, Li, Yanhong, Zhang, Lei, Yu, Hai, Li, Lei, Wang, Peng G, Chen, Xi
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Sprache:eng
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Zusammenfassung:Arabidopsis thaliana glucuronokinase (AtGlcAK) was cloned and shown to be able to use various uronic acids as substrates to produce the corresponding uronic acid-1-phosphates. AtGlcAK or Bifidobacterium infantis galactokinase (BiGalK) was used with a UDP-sugar pyrophosphorylase, an inorganic pyrophosphatase, with or without a glycosyltransferase for highly efficient synthesis of UDP-uronic acids and glucuronides. These improved cost-effective one-pot multienzyme (OPME) systems avoid the use of nicotinamide adenine dinucleotide (NAD(+))-cofactor in dehydrogenase-dependent UDP-glucuronic acid production processes and can be broadly applied for synthesizing various glucuronic acid-containing molecules.
ISSN:1359-7345
1364-548X
1364-548X
DOI:10.1039/c4cc10306h