EC Number   |
|---|
   4.1.2.22 | - |
| 4.1.2.22 | cloned in a prokaryotic vector, and the encoded protein is expressed in Escherichia coli |
| 4.1.2.22 | expressed in Escherichia coli |
| 4.1.2.22 | expressed in Escherichia coli BL21 CodonPlus (DE3)-RIL cells |
| 4.1.2.22 | expressed in Escherichia coli BL21(DE3) cells |
| 4.1.2.22 | expressed in Escherichia coli BL21(DE3)RIL cells |
| 4.1.2.22 | expressed in Escherichia coli strain BL21 (DE3) |
| 4.1.2.22 | expression in Escherichia coli |
| 4.1.2.22 | Saccharomyces cerevisiae does not demonstrate efficient phosphoketolase activity naturally. When phosphoketolase fome is expressed in Saccharomyces cerevisiae significant amounts of acetyl-phosphate are produced after provision of sugar phosphate substrates in vitro. Expression of bacterial phosphoketolase in Saccharomyces cerevisiae can efficiently divert intracellular carbon flux toward C2-synthesis, thus showing potential to be used in metabolic engineering strategies aimed to increase yields of acetyl-CoA derived compounds |
| 4.1.2.22 | Saccharomyces cerevisiae does not demonstrate efficient phosphoketolase activity naturally. When phosphoketolase from Bifidobacterium adolescentis is expressed in Saccharomyces cerevisiae significant amounts of acetyl-phosphate are produced after provision of sugar phosphate substrates in vitro. Expression of bacterial phosphoketolase in Saccharomyces cerevisiae can efficiently divert intracellular carbon flux toward C2-synthesis, thus showing potential to be used in metabolic engineering strategies aimed to increase yields of acetyl-CoA derived compounds |
