2022
DOI: 10.21203/rs.3.rs-1384627/v1
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Expression and Structural Characterization of Recombinant Mercuric Reductase Protein Isolated from Streptomyces

Abstract: Efforts to control mercury pollution have been made for the last twenty years using various biological, physical, and chemical approaches. Streptomyces is able to degrade mercury because it possesses the mercuric reductase enzyme encoded by merA. The merA from Streptomyces isolate AS2 (Accession numbers LC026157) has been cloned into the expression vector pEt-28c(+). Therefore, it is critical to study recombinant mercuric reductase protein's expression and to analyse the protein structure. Expression of merA f… Show more

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Cited by 1 publication
(2 citation statements)
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“…This was confirmed by the ability of the isolates to grow on selective LB medium with kanamycin (20 μg/ml) and the formation of approximately 40 colonies after incubation for 24 hours at 37°C. This positive result indicates the ability of the plasmid to produce target proteins [25].…”
Section: мікробіологія / Microbiologymentioning
confidence: 88%
See 1 more Smart Citation
“…This was confirmed by the ability of the isolates to grow on selective LB medium with kanamycin (20 μg/ml) and the formation of approximately 40 colonies after incubation for 24 hours at 37°C. This positive result indicates the ability of the plasmid to produce target proteins [25].…”
Section: мікробіологія / Microbiologymentioning
confidence: 88%
“…За даними Heydenreich, F.M., Miljuš, T., Jaussi,R. та інші ефективність генетичної рекомбінації суперкомпетентних клітин штаму E. coli XL1-Blue, отриманих методом Іноу, при трансформації плазмідою pBR322, яка [25].…”
Section: мікробіологія / Microbiologyunclassified