<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2013</volume><submitter>Preobrazhenskaya YV</submitter><funding>Warsaw University, Poland</funding><pubmed_abstract>The transformation of the strain DH5α (TM)-T1(R) with plasmid vector pET11a containing the cloned gene of bacterial selenophosphate synthetase (SPS), selD, from the E. coli BL21-Gold (DE3) strain gives an overproducing strain of SPS with one synonymic substitution, E197D. The transformation efficiency was estimated as 8 × 10(8) CFU/ μ g plasmid DNA. 28 mg of highly purified preparation of recombinant SPS capable of binding TNP-ATP was eluted from DEAE-Sephadex column in amount of 15 % from the total soluble protein in crude extract. The fluorescent derivative of ATP, 2'(3')-O-(2,4,6-trinitrophenyl)adenosine-5'-triphosphate (TNP-ATP), was used as a synthetic analog of the substrate for the monitoring and quantitative analysis of the functional activity of SPS. The non-linear regression anal</pubmed_abstract><journal>Journal of amino acids</journal><pagination>983565</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3956282</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Binding Stoichiometry of a Recombinant Selenophosphate Synthetase with One Synonymic Substitution E197D to a Fluorescent Nucleotide Analog of ATP, TNP-ATP.</pubmed_title><pmcid>PMC3956282</pmcid><pubmed_authors>Stenko AI</pubmed_authors><pubmed_authors>Lugovtsev VY</pubmed_authors><pubmed_authors>Preobrazhenskaya YV</pubmed_authors><pubmed_authors>Shvarts MV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Binding Stoichiometry of a Recombinant Selenophosphate Synthetase with One Synonymic Substitution E197D to a Fluorescent Nucleotide Analog of ATP, TNP-ATP.</name><description>The transformation of the strain DH5α (TM)-T1(R) with plasmid vector pET11a containing the cloned gene of bacterial selenophosphate synthetase (SPS), selD, from the E. coli BL21-Gold (DE3) strain gives an overproducing strain of SPS with one synonymic substitution, E197D. The transformation efficiency was estimated as 8 × 10(8) CFU/ μ g plasmid DNA. 28 mg of highly purified preparation of recombinant SPS capable of binding TNP-ATP was eluted from DEAE-Sephadex column in amount of 15 % from the total soluble protein in crude extract. The fluorescent derivative of ATP, 2'(3')-O-(2,4,6-trinitrophenyl)adenosine-5'-triphosphate (TNP-ATP), was used as a synthetic analog of the substrate for the monitoring and quantitative analysis of the functional activity of SPS. The non-linear regression anal</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013</publication><modification>2025-04-04T22:45:50.775Z</modification><creation>2019-03-27T01:23:31Z</creation></dates><accession>S-EPMC3956282</accession><cross_references><pubmed>24719756</pubmed><doi>10.1155/2013/983565</doi></cross_references></HashMap>