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

Verfasser / Beitragende:
[Lennart Leßmeier, Johannes Pfeifenschneider, Marc Carnicer, Stephanie Heux, Jean-Charles Portais, Volker Wendisch]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/23(2015-12-01), 10163-10176
Format:
Artikel (online)
ID: 605504822
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024 7 0 |a 10.1007/s00253-015-6906-5  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-015-6906-5 
245 0 0 |a Production of carbon-13-labeled cadaverine by engineered Corynebacterium glutamicum using carbon-13-labeled methanol as co-substrate  |h [Elektronische Daten]  |c [Lennart Leßmeier, Johannes Pfeifenschneider, Marc Carnicer, Stephanie Heux, Jean-Charles Portais, Volker Wendisch] 
520 3 |a 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. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Methylotrophy  |2 nationallicence 
690 7 |a Methanol  |2 nationallicence 
690 7 |a Corynebacterium glutamicum  |2 nationallicence 
690 7 |a Cadaverine  |2 nationallicence 
690 7 |a Diaminopentane  |2 nationallicence 
690 7 |a 13C-labeling  |2 nationallicence 
690 7 |a Bacillus methanolicus  |2 nationallicence 
700 1 |a Leßmeier  |D Lennart  |u Genetics of Prokaryotes, Faculty of Biology and Center for Biotechnology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany  |4 aut 
700 1 |a Pfeifenschneider  |D Johannes  |u Genetics of Prokaryotes, Faculty of Biology and Center for Biotechnology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany  |4 aut 
700 1 |a Carnicer  |D Marc  |u LISBP-INSA de Toulouse, 135 avenue de Rangueil, 31077, Toulouse CEDEX 04, France  |4 aut 
700 1 |a Heux  |D Stephanie  |u LISBP-INSA de Toulouse, 135 avenue de Rangueil, 31077, Toulouse CEDEX 04, France  |4 aut 
700 1 |a Portais  |D Jean-Charles  |u LISBP-INSA de Toulouse, 135 avenue de Rangueil, 31077, Toulouse CEDEX 04, France  |4 aut 
700 1 |a Wendisch  |D Volker  |u Genetics of Prokaryotes, Faculty of Biology and Center for Biotechnology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/23(2015-12-01), 10163-10176  |x 0175-7598  |q 99:23<10163  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-015-6906-5  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Leßmeier  |D Lennart  |u Genetics of Prokaryotes, Faculty of Biology and Center for Biotechnology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Pfeifenschneider  |D Johannes  |u Genetics of Prokaryotes, Faculty of Biology and Center for Biotechnology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Carnicer  |D Marc  |u LISBP-INSA de Toulouse, 135 avenue de Rangueil, 31077, Toulouse CEDEX 04, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Heux  |D Stephanie  |u LISBP-INSA de Toulouse, 135 avenue de Rangueil, 31077, Toulouse CEDEX 04, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Portais  |D Jean-Charles  |u LISBP-INSA de Toulouse, 135 avenue de Rangueil, 31077, Toulouse CEDEX 04, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Wendisch  |D Volker  |u Genetics of Prokaryotes, Faculty of Biology and Center for Biotechnology, Bielefeld University, Universitätsstraße 25, 33615, Bielefeld, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/23(2015-12-01), 10163-10176  |x 0175-7598  |q 99:23<10163  |1 2015  |2 99  |o 253