AbstractThe cDNA coding for rat S-adenosylmethionine decarboxylase (AdoMetDC, EC 4.1.1.50) has been cloned into a plasmid expression vector, pKK-223-3, and expressed in E. coli. The authenticity of the expressed protein has been demonstrated by reactivity with antibodies specific for rat Ado-MetDC, by size analysis on SDS gels visualized with immunotransblots, and, finally, by catalytic activity. The expression of the enzyme results in a decrease in the activity of the bacterial enzyme suggesting the replacement of the bacterial enzyme by the rat AdoMetDC. Similarly, the addition of exogenous spermidine to the growth medium reduces bacterial enzyme activity affecting only marginally the expression of the recombinant protein
AbstractThe activity of S-adenosylmethionine decarboxylase (AdoMetDC) in Crithidia fasciculata was s...
Plasmodium falciparum like other organisms is dependent on polyamines for proliferation. Polyamine b...
The short-lived enzyme S-adenosylmethionine decarboxylase uses a covalently bound pyruvoyl cofactor ...
AbstractThe cDNA coding for rat S-adenosylmethionine decarboxylase (AdoMetDC, EC 4.1.1.50) has been ...
AbstractThe gene for S-adenosylmethionine decarboxylase (AdoMetDC) was isolated from a rat genomic l...
In order to understand the structure and regulation of S-adenosylmethionine decarboxylase, cDNA clon...
The coding region nucleotide sequences of rat, hamster, and bovine S-adenosylmethionine decarboxylas...
S-Adenosylmethionine decarboxylase is a key enzyme in the biosynthesis of polyamines that is the rat...
S-adenosylmethionine decarboxylase (AdoMetDC) is a key enzyme in the biosynthesis of the polyamines ...
S-adenosylmethionine decarboxylase (AdoMetDC) catalyzes the formation of decarboxylated AdoMetDC, a ...
Treatment of L1210 cells with either of two inhibitors of S-adenosylmethionine decarboxylase (AdoMet...
Adenosyl Methionine (SAMe) Synthetase is an enzyme which catalyses the synthesis of S-Adenosyl Methi...
The activity of S-adenosyl-L-methionine Decarboxylase (E. C. 4.1.1.50) was measured in two different...
S-Adenosyl Methionine (SAMe) Synthetase is an enzyme which catalyses the synthesis of S-Adenosyl Met...
1. S-adenosylmethionine decarboxylase from human placenta has been purified more than 1200-fold by u...
AbstractThe activity of S-adenosylmethionine decarboxylase (AdoMetDC) in Crithidia fasciculata was s...
Plasmodium falciparum like other organisms is dependent on polyamines for proliferation. Polyamine b...
The short-lived enzyme S-adenosylmethionine decarboxylase uses a covalently bound pyruvoyl cofactor ...
AbstractThe cDNA coding for rat S-adenosylmethionine decarboxylase (AdoMetDC, EC 4.1.1.50) has been ...
AbstractThe gene for S-adenosylmethionine decarboxylase (AdoMetDC) was isolated from a rat genomic l...
In order to understand the structure and regulation of S-adenosylmethionine decarboxylase, cDNA clon...
The coding region nucleotide sequences of rat, hamster, and bovine S-adenosylmethionine decarboxylas...
S-Adenosylmethionine decarboxylase is a key enzyme in the biosynthesis of polyamines that is the rat...
S-adenosylmethionine decarboxylase (AdoMetDC) is a key enzyme in the biosynthesis of the polyamines ...
S-adenosylmethionine decarboxylase (AdoMetDC) catalyzes the formation of decarboxylated AdoMetDC, a ...
Treatment of L1210 cells with either of two inhibitors of S-adenosylmethionine decarboxylase (AdoMet...
Adenosyl Methionine (SAMe) Synthetase is an enzyme which catalyses the synthesis of S-Adenosyl Methi...
The activity of S-adenosyl-L-methionine Decarboxylase (E. C. 4.1.1.50) was measured in two different...
S-Adenosyl Methionine (SAMe) Synthetase is an enzyme which catalyses the synthesis of S-Adenosyl Met...
1. S-adenosylmethionine decarboxylase from human placenta has been purified more than 1200-fold by u...
AbstractThe activity of S-adenosylmethionine decarboxylase (AdoMetDC) in Crithidia fasciculata was s...
Plasmodium falciparum like other organisms is dependent on polyamines for proliferation. Polyamine b...
The short-lived enzyme S-adenosylmethionine decarboxylase uses a covalently bound pyruvoyl cofactor ...