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Production of carbon-13-labeled cadaverine by engineered Corynebacterium glutamicum using carbon-13-labeled methanol as co-substrate

Title: Production of carbon-13-labeled cadaverine by engineered Corynebacterium glutamicum using carbon-13-labeled methanol as co-substrate
Authors: Lessmeier, L.; Pfeifenschneider, J.; Carnicer Heras, Marc; Heux, Stephanie; Portais, Jean-Charles; Wendisch, V. F.
Contributors: Genetics of Prokaryotes, Faculty of Biology and Center for Biotechnology; Universität Bielefeld = Bielefeld University; Laboratoire d'Ingénierie des Systèmes Biologiques et des Procédés (LISBP); Institut National de la Recherche Agronomique (INRA)-Institut National des Sciences Appliquées - Toulouse (INSA Toulouse); Institut National des Sciences Appliquées (INSA)-Communauté d'universités et établissements de Toulouse (Comue de Toulouse)-Institut National des Sciences Appliquées (INSA)-Communauté d'universités et établissements de Toulouse (Comue de Toulouse)-Centre National de la Recherche Scientifique (CNRS)
Source: ISSN: 0175-7598.
Publisher Information: CCSD; Springer Verlag
Publication Year: 2015
Collection: Institut National de la Recherche Agronomique: ProdINRA
Subject Terms: Bacillus methanolicus; 13C-labeling; diaminopentane; cadaverine; Corynebacterium glutamicum; methanol; methylotrophy; [SDV.BIO]Life Sciences [q-bio]/Biotechnology
Description: Methanol, a one-carbon compound, can be utilized by a variety of bacteria and other organisms as carbon and energy source and is regarded as a promising substrate for biotechnological production. In this study, a strain of non-methylotrophic Corynebacterium glutamicum, which was able to produce the polyamide building block cadaverine as non-native product, was engineered for co-utilization of methanol. Expression of the gene encoding NAD+-dependent methanol dehydrogenase (Mdh) from the natural methylotroph Bacillus methanolicus increased methanol oxidation. Deletion of the endogenous aldehyde dehydrogenase genes ald and fadH prevented methanol oxidation to carbon dioxide and formaldehyde detoxification via the linear formaldehyde dissimilation pathway. Heterologous expression of genes for the key enzymes hexulose-6-phosphate synthase and 6-phospho-3-hexuloisomerase of the ribulose monophosphate (RuMP) pathway in this strain restored growth in the presence of methanol or formaldehyde, which suggested efficient formaldehyde detoxification involving RuMP key enzymes. While growth with methanol as sole carbon source was not observed, the fate of 13C-methanol added as co-substrate to sugars was followed and the isotopologue distribution indicated incorporation into central metabolites and in vivo activity of the RuMP pathway. In addition, 13C-label from methanol was traced to the secreted product cadaverine. Thus, this synthetic biology approach led to a C. glutamicum strain that converted the non-natural carbon substrate methanol at least partially to the non-native product cadaverine.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/26276544; PRODINRA: 320970; PUBMED: 26276544; WOS: 000365171600025
DOI: 10.1007/s00253-015-6906-5
Availability: https://hal.science/hal-01269204; https://hal.science/hal-01269204v1/document; https://hal.science/hal-01269204v1/file/2015-Leissmeyer%20et%20al-mod.pdf; https://doi.org/10.1007/s00253-015-6906-5
Rights: https://about.hal.science/hal-authorisation-v1/ ; info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.6744EBD7
Database: BASE