A de novo NADPH generation pathway for improving lysine production of Corynebacterium glutamicum by rational design of the coenzyme specificity of glyceraldehyde 3-phosphate dehydrogenase
Autor: | Zhen Chen, Rajesh Reddy Bommareddy, Sugima Rappert, An-Ping Zeng |
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Rok vydání: | 2014 |
Předmět: |
Lysine
Bioengineering Dehydrogenase Biology Pentose phosphate pathway Applied Microbiology and Biotechnology Cofactor Corynebacterium glutamicum Genetic Enhancement Biochemistry Metabolic Engineering biology.protein Coenzyme binding NAD+ kinase Flux (metabolism) Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) Glyceraldehyde 3-phosphate dehydrogenase NADP Biotechnology Signal Transduction |
Zdroj: | Metabolic engineering. 25 |
ISSN: | 1096-7184 |
Popis: | Engineering the cofactor availability is a common strategy of metabolic engineering to improve the production of many industrially important compounds. In this work, a de novo NADPH generation pathway is proposed by altering the coenzyme specificity of a native NAD-dependent glyceraldehyde 3-phosphate dehydrogenase (GAPDH) to NADP, which consequently has the potential to produce additional NADPH in the glycolytic pathway. Specifically, the coenzyme specificity of GAPDH of Corynebacterium glutamicum is systematically manipulated by rational protein design and the effect of the manipulation for cellular metabolism and lysine production is evaluated. By a combinatorial modification of four key residues within the coenzyme binding sites, different GAPDH mutants with varied coenzyme specificity were constructed. While increasing the catalytic efficiency of GAPDH towards NADP enhanced lysine production in all of the tested mutants, the most significant improvement of lysine production (~60%) was achieved with the mutant showing similar preference towards both NAD and NADP. Metabolic flux analysis with (13)C isotope studies confirmed that there was no significant change of flux towards the pentose phosphate pathway and the increased lysine yield was mainly attributed to the NADPH generated by the mutated GAPDH. The present study highlights the importance of protein engineering as a key strategy in de novo pathway design and overproduction of desired products. |
Databáze: | OpenAIRE |
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