<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Simioni B</submitter><funding>Fundação Araucária</funding><funding>Superintendência Geral de Ciência, Tecnologia e Ensino Superior do Estado do Paraná</funding><funding>CNPq</funding><pagination>2367</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12566495</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(10)</volume><pubmed_abstract>The present study investigated the impact of genetic engineering strategies to produce a cell-free xylanase for applications in the baking industry. The &lt;i>xynA1&lt;/i> gene from the nonpathogenic bacterium &lt;i>Caulobacter vibrioides&lt;/i> was integrated into the pAS22 vector with a xylose-inducible promoter and introduced back into the bacteria, resulting in the creation of the BS-&lt;i>xynA1&lt;/i>. This construct exhibited substantial secreted xylanase 1 (XynA1) activity, reaching 17.22 U/mL, and a specific activity of 278.64 U/mg after an 18 h growth period with 0.3% (&lt;i>v&lt;/i>/&lt;i>v&lt;/i>) xylose plus 0.2% (&lt;i>w&lt;/i>/&lt;i>v&lt;/i>) corn straw. RT-qPCR analysis confirmed that higher xylanase activity in &lt;i>C. vibrioides&lt;/i> cells was correlated with increased transcription of the &lt;i>xynA1&lt;/i> gene in the in</pubmed_abstract><journal>Microorganisms</journal><pubmed_title>Bioengineering &amp;lt;i&amp;gt;Caulobacter vibrioides&amp;lt;/i&amp;gt; for Xylanase Applications in the Bakery Industry.</pubmed_title><pmcid>PMC12566495</pmcid><funding_grant_id>Emenda Governamental-EG n◦ 14/2024-Termo de Execução Descentralizada -TED n◦ 032/2025</funding_grant_id><funding_grant_id>Project nº: PRD2023361000397 Agreement nº 180/2025 PDI</funding_grant_id><funding_grant_id>Universal Grant: 407596/2023-2</funding_grant_id><pubmed_authors>Rocha PMC</pubmed_authors><pubmed_authors>Maller A</pubmed_authors><pubmed_authors>Gandra RF</pubmed_authors><pubmed_authors>Kadowaki MK</pubmed_authors><pubmed_authors>Simioni B</pubmed_authors><pubmed_authors>Favero A</pubmed_authors><pubmed_authors>da Conceicao Silva JL</pubmed_authors><pubmed_authors>Simao RCG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bioengineering &amp;lt;i&amp;gt;Caulobacter vibrioides&amp;lt;/i&amp;gt; for Xylanase Applications in the Bakery Industry.</name><description>The present study investigated the impact of genetic engineering strategies to produce a cell-free xylanase for applications in the baking industry. The &lt;i>xynA1&lt;/i> gene from the nonpathogenic bacterium &lt;i>Caulobacter vibrioides&lt;/i> was integrated into the pAS22 vector with a xylose-inducible promoter and introduced back into the bacteria, resulting in the creation of the BS-&lt;i>xynA1&lt;/i>. This construct exhibited substantial secreted xylanase 1 (XynA1) activity, reaching 17.22 U/mL, and a specific activity of 278.64 U/mg after an 18 h growth period with 0.3% (&lt;i>v&lt;/i>/&lt;i>v&lt;/i>) xylose plus 0.2% (&lt;i>w&lt;/i>/&lt;i>v&lt;/i>) corn straw. RT-qPCR analysis confirmed that higher xylanase activity in &lt;i>C. vibrioides&lt;/i> cells was correlated with increased transcription of the &lt;i>xynA1&lt;/i> gene in the in</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-05-14T03:21:31.87Z</modification><creation>2026-05-14T03:12:49.253Z</creation></dates><accession>S-EPMC12566495</accession><cross_references><pubmed>41156826</pubmed><doi>10.3390/microorganisms13102367</doi></cross_references></HashMap>