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Cloned (Commentary)
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a pPTB construct is used, expression experiments are performed in Escherichia coli cells; into the pBAD-TOPO vector, furthermore a pTRC construct is used, expression experiments are performed in Escherichia coli cells
cloned from the VIN13 commercial wine yeast strain, and placed under the constitutive control of the PGK1 regulatory sequences. Overexpression of ATF1 in vine yeast significantly increased the concentrations of ethyl acetate, isoamyl acetate, 2-phenylethyl acetate and ethyl caproate; cloned from the VIN13 commercial wine yeast strain, and placed under the constitutive control of the PGK1 regulatory sequences to generate plasmids pATF2-s. Overexpression of ATF2 in vine yeast increased the concentrations of ethyl acetate and isoamyl acetate to a lesser degree than overexpression of ATF1
cloning of ATF1 and ATF2 genes encoding alcohol acetyltransferases
cloning of ATF1 gene encoding alcohol acetyltransferase, expression in Saccharomyces cerevisiae
cloning of Lg-ATF1 gene encoding alcohol acetyltransferase, expression in Saccharomyces cerevisiae
cloning of the ATF1 gene encoding alcohol acetyltransferase 1 from wine yeast
complete coding region of PhCFAT cDNA subcloned into expression vector pET-28a and expressed in Escherichia coli
expression in Escherichia coli
expression in Escherichia coli, alcohol acetyltransferase AFT1; expression in Escherichia coli and in Clostridium acetobutylicum, alcohol acetyltransferase AFT2
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