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Enhancing the light-driven production of d-lactate by engineering cyanobacterium using a combinational strategy

It is increasingly attractive to engineer cyanobacteria for bulk production of chemicals from CO(2). However, cofactor bias of cyanobacteria is different from bacteria that prefer NADH, which hampers cyanobacterial strain engineering. In this study, the key enzyme d-lactate dehydrogenase (LdhD) from...

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Detalles Bibliográficos
Autores principales: Li, Chao, Tao, Fei, Ni, Jun, Wang, Yu, Yao, Feng, Xu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419521/
https://www.ncbi.nlm.nih.gov/pubmed/25940225
http://dx.doi.org/10.1038/srep09777
Descripción
Sumario:It is increasingly attractive to engineer cyanobacteria for bulk production of chemicals from CO(2). However, cofactor bias of cyanobacteria is different from bacteria that prefer NADH, which hampers cyanobacterial strain engineering. In this study, the key enzyme d-lactate dehydrogenase (LdhD) from Lactobacillus bulgaricus ATCC11842 was engineered to reverse its favored cofactor from NADH to NADPH. Then, the engineered enzyme was introduced into Synechococcus elongatus PCC7942 to construct an efficient light-driven system that produces d-lactic acid from CO(2). Mutation of LdhD drove a fundamental shift in cofactor preference towards NADPH, and increased d-lactate productivity by over 3.6-fold. We further demonstrated that introduction of a lactic acid transporter and bubbling CO(2)-enriched air also enhanced d-lactate productivity. Using this combinational strategy, increased d-lactate concentration and productivity were achieved. The present strategy may also be used to engineer cyanobacteria for producing other useful chemicals.