<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-29T17:03:09Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/22776" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/22776</identifier><datestamp>2024-11-28T20:32:03Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16967</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Prezioso, Samantha M</subfield>
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      <subfield code="a">Duong, Duc M</subfield>
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      <subfield code="a">Kuiper, Emily G</subfield>
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      <subfield code="a">Deng, Qiudong</subfield>
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      <subfield code="a">Alberti, Sebastian</subfield>
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      <subfield code="a">Conn, Graeme L</subfield>
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      <subfield code="a">Goldberg, Joanna B</subfield>
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      <subfield code="c">2019-03-05</subfield>
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      <subfield code="a">The Pseudomonas aeruginosa methyltransferase EftM trimethylates elongation factor-Tu (EF-Tu) on lysine 5 to form a post-translational modification important for initial bacterial adherence to host epithelial cells. EftM methyltransferase activity is directly temperature regulated. The protein stability of EftM is tuned with a melting temperature (T-m) around 37 degrees C such that the enzyme is stable and active at 25 degrees C, but is completely inactivated by protein unfolding at higher temperatures. This leads to higher observable levels of EF-Tu trimethylation at the lower temperature. Here we report an additional layer of thermoregulation resulting in lower eftM mRNA transcript level at 37 degrees C compared to 25 degrees C and show that this regulation occurs at the level of transcription initiation. To begin to define the impact of this system on P. aeruginosa physiology, we demonstrate that EF-Tu is the only observable substrate for EftM. Further, we interrogated the proteome of three different wild-type P. aeruginosa strains, their eftM mutants, and these mutants complemented with eftM and conclude that trimethylation of EF-Tu by EftM does not impact EF-Tu's canonical function in translation. In addition to furthering our knowledge of this Pseudomonas virulence factor, this study provides an intriguing example of a protein with multiple layers of thermoregulation.</subfield>
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      <subfield code="a">Prezioso SM, Duong DM, Kuiper EG, Deng Q, Alberti S, Conn GL, et al. Trimethylation of Elongation Factor-Tu by the Dual Thermoregulated Methyltransferase EftM Does Not Impact Its Canonical Function in Translation. Sci Rep. 2019 Mar 05;9:3553.</subfield>
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      <subfield code="a">10.1038/s41598-019-39331-x</subfield>
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      <subfield code="a">2045-2322</subfield>
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      <subfield code="a">Scientific Reports</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.13003/17595</subfield>
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      <subfield code="a">30837495</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/22776</subfield>
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      <subfield code="a">460381600126</subfield>
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      <subfield code="a">Trimethylation of Elongation Factor-Tu by the Dual Thermoregulated Methyltransferase EftM Does Not Impact Its Canonical Function in Translation</subfield>
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