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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.
Afiliación
  • Vortmann M; Institute for Biology and Biotechnology of Plants, University of Münster, Schlossplatz 8, 48143, Münster, Germany.
  • Stumpf AK; Institute for Molecular Microbiology and Biotechnology, University of Münster, Corrensstr. 3, 48149, Münster, Germany.
  • Sgobba E; Chair of Genetics of Prokaryotes, Faculty of Biology & CeBiTec, University of Bielefeld, P.O. Box 100131, 33501, Bielefeld, Germany.
  • Dirks-Hofmeister ME; Department of Forest Genetics and Plant Physiology, SLU, Skogsmarksgränd 17, 90183, Umeå, Sweden.
  • Krehenbrink M; WeissBioTech GmbH, An der Hansalinie 48-50, 59387, Ascheberg, Germany.
  • Wendisch VF; Cysal GmbH, Mendelstraße 11, 48149, Münster, Germany.
  • Philipp B; Chair of Genetics of Prokaryotes, Faculty of Biology & CeBiTec, University of Bielefeld, P.O. Box 100131, 33501, Bielefeld, Germany.
  • Moerschbacher BM; Institute for Molecular Microbiology and Biotechnology, University of Münster, Corrensstr. 3, 48149, Münster, Germany.
Appl Microbiol Biotechnol ; 105(4): 1547-1561, 2021 Feb.
Article en En | MEDLINE | ID: mdl-33521845
ABSTRACT
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 GlcNAc2, chitin deacetylase to convert GlcNAc2 into GlcN2 and acetate, and glucosaminidase to cleave GlcN2 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 ß-1,4-glucosaminidase degraded chitin to GlcNAc2 or GlcN2 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. 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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Quitinasas / Corynebacterium glutamicum Idioma: En Revista: Appl Microbiol Biotechnol Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Quitinasas / Corynebacterium glutamicum Idioma: En Revista: Appl Microbiol Biotechnol Año: 2021 Tipo del documento: Article