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A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine

Chitin is an abundant waste product from shrimp and mushroom industries and as such, an appropriate secondary feedstock for biotechnological processes. However, chitin is a crystalline substrate embedded in complex biological matrices, and, therefore, difficult to utilize, requiring an equally compl...

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Autores principales: Vortmann, Marina, Stumpf, Anna K., Sgobba, Elvira, Dirks-Hofmeister, Mareike E., Krehenbrink, Martin, Wendisch, Volker F., Philipp, Bodo, Moerschbacher, Bruno M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880967/
https://www.ncbi.nlm.nih.gov/pubmed/33521845
http://dx.doi.org/10.1007/s00253-021-11112-5
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author Vortmann, Marina
Stumpf, Anna K.
Sgobba, Elvira
Dirks-Hofmeister, Mareike E.
Krehenbrink, Martin
Wendisch, Volker F.
Philipp, Bodo
Moerschbacher, Bruno M.
author_facet Vortmann, Marina
Stumpf, Anna K.
Sgobba, Elvira
Dirks-Hofmeister, Mareike E.
Krehenbrink, Martin
Wendisch, Volker F.
Philipp, Bodo
Moerschbacher, Bruno M.
author_sort Vortmann, Marina
collection PubMed
description Chitin is an abundant waste product from shrimp and mushroom industries and as such, an appropriate secondary feedstock for biotechnological processes. However, chitin is a crystalline substrate embedded in complex biological matrices, and, therefore, difficult to utilize, requiring an equally complex chitinolytic machinery. Following a bottom-up approach, we here describe the step-wise development of a mutualistic, non-competitive consortium in which a lysine-auxotrophic Escherichia coli substrate converter cleaves the chitin monomer N-acetylglucosamine (GlcNAc) into glucosamine (GlcN) and acetate, but uses only acetate while leaving GlcN for growth of the lysine-secreting Corynebacterium glutamicum producer strain. We first engineered the substrate converter strain for growth on acetate but not GlcN, and the producer strain for growth on GlcN but not acetate. Growth of the two strains in co-culture in the presence of a mixture of GlcN and acetate was stabilized through lysine cross-feeding. Addition of recombinant chitinase to cleave chitin into GlcNAc(2), chitin deacetylase to convert GlcNAc(2) into GlcN(2) and acetate, and glucosaminidase to cleave GlcN(2) into GlcN supported growth of the two strains in co-culture in the presence of colloidal chitin as sole carbon source. Substrate converter strains secreting a chitinase or a β-1,4-glucosaminidase degraded chitin to GlcNAc(2) or GlcN(2) to GlcN, respectively, but required glucose for growth. In contrast, by cleaving GlcNAc into GlcN and acetate, a chitin deacetylase-expressing substrate converter enabled growth of the producer strain in co-culture with GlcNAc as sole carbon source, providing proof-of-principle for a fully integrated co-culture for the biotechnological utilization of chitin. [Image: see text] Key Points • A bacterial consortium was developed to use chitin as feedstock for the bioeconomy. • Substrate converter and producer strain use different chitin hydrolysis products. • Substrate converter and producer strain are mutually dependent on each other. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-021-11112-5.
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spelling pubmed-78809672021-02-18 A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine Vortmann, Marina Stumpf, Anna K. Sgobba, Elvira Dirks-Hofmeister, Mareike E. Krehenbrink, Martin Wendisch, Volker F. Philipp, Bodo Moerschbacher, Bruno M. Appl Microbiol Biotechnol Applied Genetics and Molecular Biotechnology Chitin is an abundant waste product from shrimp and mushroom industries and as such, an appropriate secondary feedstock for biotechnological processes. However, chitin is a crystalline substrate embedded in complex biological matrices, and, therefore, difficult to utilize, requiring an equally complex chitinolytic machinery. Following a bottom-up approach, we here describe the step-wise development of a mutualistic, non-competitive consortium in which a lysine-auxotrophic Escherichia coli substrate converter cleaves the chitin monomer N-acetylglucosamine (GlcNAc) into glucosamine (GlcN) and acetate, but uses only acetate while leaving GlcN for growth of the lysine-secreting Corynebacterium glutamicum producer strain. We first engineered the substrate converter strain for growth on acetate but not GlcN, and the producer strain for growth on GlcN but not acetate. Growth of the two strains in co-culture in the presence of a mixture of GlcN and acetate was stabilized through lysine cross-feeding. Addition of recombinant chitinase to cleave chitin into GlcNAc(2), chitin deacetylase to convert GlcNAc(2) into GlcN(2) and acetate, and glucosaminidase to cleave GlcN(2) into GlcN supported growth of the two strains in co-culture in the presence of colloidal chitin as sole carbon source. Substrate converter strains secreting a chitinase or a β-1,4-glucosaminidase degraded chitin to GlcNAc(2) or GlcN(2) to GlcN, respectively, but required glucose for growth. In contrast, by cleaving GlcNAc into GlcN and acetate, a chitin deacetylase-expressing substrate converter enabled growth of the producer strain in co-culture with GlcNAc as sole carbon source, providing proof-of-principle for a fully integrated co-culture for the biotechnological utilization of chitin. [Image: see text] Key Points • A bacterial consortium was developed to use chitin as feedstock for the bioeconomy. • Substrate converter and producer strain use different chitin hydrolysis products. • Substrate converter and producer strain are mutually dependent on each other. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-021-11112-5. Springer Berlin Heidelberg 2021-02-01 2021 /pmc/articles/PMC7880967/ /pubmed/33521845 http://dx.doi.org/10.1007/s00253-021-11112-5 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Applied Genetics and Molecular Biotechnology
Vortmann, Marina
Stumpf, Anna K.
Sgobba, Elvira
Dirks-Hofmeister, Mareike E.
Krehenbrink, Martin
Wendisch, Volker F.
Philipp, Bodo
Moerschbacher, Bruno M.
A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine
title A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine
title_full A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine
title_fullStr A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine
title_full_unstemmed A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine
title_short A bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine
title_sort bottom-up approach towards a bacterial consortium for the biotechnological conversion of chitin to l-lysine
topic Applied Genetics and Molecular Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880967/
https://www.ncbi.nlm.nih.gov/pubmed/33521845
http://dx.doi.org/10.1007/s00253-021-11112-5
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