{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,29]],"date-time":"2025-09-29T03:46:53Z","timestamp":1759117613352},"reference-count":29,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2012,3,12]],"date-time":"2012-03-12T00:00:00Z","timestamp":1331510400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Biotech and App Biochem"],"published-print":{"date-parts":[[2012,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Prolactin (PRL) is a pleiotropic hormone produced by lactotroph cells of the anterior pituitary gland and is mainly related to lactation control and reproduction. Recombinant mouse prolactin (r\u2010mPRL), never obtained in its authentic form, can be very useful for research and tests in animal models, in which human prolactin (hPRL) is usually employed in a heterologous mode. Synthesis of r\u2010mPRL was carried out here via secretion in <jats:italic>Escherichia coli<\/jats:italic> periplasmic space using a plasmid containing mPRL cDNA joined to the DsbA signal peptide sequence under the control of a constitutive major leftward promoter of the bacteriophage <jats:italic>\u03bb<\/jats:italic> (<jats:italic>\u03bb<\/jats:italic><jats:sub>PL<\/jats:sub>). Fermentation in a pilot bioreactor was carried out at 30\u00b0C, with 6 H of induction at 37\u00b0C, reaching an optical density of 23 A<jats:sub>600<\/jats:sub> units, a specific yield of 0.06\u20130.1 \u00b5g mPRL\/(mL A<jats:sub>600<\/jats:sub>), and a concentration of up to 2.2 \u00b5g\/mL. Even with such a low yield and a poor mass fraction, r\u2010mPRL was purified via a three\u2010step laboratory process based on hydrophobic chromatography, reversed\u2010phase high\u2010performance liquid chromatography, and high\u2010performance size\u2010exclusion chromatography (HPSEC). The purified hormone was then characterized using SDS\u2010PAGE, Western blotting, and HPSEC and showed, by Nb2 rat lymphoma cell proliferation assay, a bioactivity of 39.5 IU\/mg, determined against the International Standard of recombinant hPRL [World Health Organization (WHO)\u201097\/714].<\/jats:p>","DOI":"10.1002\/bab.1008","type":"journal-article","created":{"date-parts":[[2012,3,12]],"date-time":"2012-03-12T18:38:44Z","timestamp":1331577524000},"page":"178-185","source":"Crossref","is-referenced-by-count":13,"title":["Expression, purification, and characterization of authentic mouse prolactin obtained in <i>Escherichia coli<\/i> periplasmic space"],"prefix":"10.1002","volume":"59","author":[{"given":"Miriam F.","family":"Suzuki","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fernanda S.","family":"Arthuso","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jo\u00e3o E.","family":"Oliveira","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N\u00e9lio A. 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