<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Srirangan K</submitter><funding>Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada</funding><funding>Gouvernement du Canada | Networks of Centres of Excellence of Canada</funding><funding>Canada Research Chairs</funding><pagination>2574-2584</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4836414</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>82(9)</volume><pubmed_abstract>To expand the chemical and molecular diversity of biotransformation using whole-cell biocatalysts, we genetically engineered a pathway in Escherichia coli for heterologous production of butanone, an important commodity ketone. First, a 1-propanol-producing E. coli host strain with its sleeping beauty mutase (Sbm) operon being activated was used to increase the pool of propionyl-coenzyme A (propionyl-CoA). Subsequently, molecular heterofusion of propionyl-CoA and acetyl-CoA was conducted to yield 3-ketovaleryl-CoA via a CoA-dependent elongation pathway. Lastly, 3-ketovaleryl-CoA was channeled into the clostridial acetone formation pathway for thioester hydrolysis and subsequent decarboxylation to form butanone. Biochemical, genetic, and metabolic factors affecting relative levels of ketogen</pubmed_abstract><journal>Applied and environmental microbiology</journal><pubmed_title>Engineering Escherichia coli for Microbial Production of Butanone.</pubmed_title><pmcid>PMC4836414</pmcid><funding_grant_id>430106-12</funding_grant_id><funding_grant_id>950-211471</funding_grant_id><funding_grant_id>BioFuelNet Canada</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Bruder M</pubmed_authors><pubmed_authors>Srirangan K</pubmed_authors><pubmed_authors>Chou CP</pubmed_authors><pubmed_authors>Moo-Young M</pubmed_authors><pubmed_authors>Akawi L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Engineering Escherichia coli for Microbial Production of Butanone.</name><description>To expand the chemical and molecular diversity of biotransformation using whole-cell biocatalysts, we genetically engineered a pathway in Escherichia coli for heterologous production of butanone, an important commodity ketone. First, a 1-propanol-producing E. coli host strain with its sleeping beauty mutase (Sbm) operon being activated was used to increase the pool of propionyl-coenzyme A (propionyl-CoA). Subsequently, molecular heterofusion of propionyl-CoA and acetyl-CoA was conducted to yield 3-ketovaleryl-CoA via a CoA-dependent elongation pathway. Lastly, 3-ketovaleryl-CoA was channeled into the clostridial acetone formation pathway for thioester hydrolysis and subsequent decarboxylation to form butanone. Biochemical, genetic, and metabolic factors affecting relative levels of ketogen</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 May</publication><modification>2025-04-04T11:41:36.548Z</modification><creation>2019-03-27T02:11:55Z</creation></dates><accession>S-EPMC4836414</accession><cross_references><pubmed>26896132</pubmed><doi>10.1128/AEM.03964-15</doi><doi>10.1128/aem.03964-15</doi></cross_references></HashMap>