Engineering an acetoacetyl-CoA reductase from Cupriavidus necator toward NADH preference under physiological conditions

Autor(es)

Olavarria, Karel ; Pijman, Yared O. ; Cabrera, Ricardo ; van Loosdrecht, Mark C. M. ; Wahl, S. Aljoscha

• Tipo de documento: Artigo Científico
• Fonte: SCIENTIFIC REPORTS; v. 12, n. 1, p. 10-pg., 2022-03-08.

Resumo

The coupling of PHB generation with NADH reoxidation is required to generate PHB as a fermentation product. A fundamental trait to accomplish this feature is to express a functional NADH-preferring acetoacetyl-CoA reductase, engaged in PHB accumulation. One way to obtain such a reductase is by engineering the cofactor preference of the acetoacetyl-CoA reductase encoded by the phaB1 gene from Cupriavidus necator (AAR(Cn1)). Aiming to have a deeper understanding of the structural determinants of the cofactor preference in AAR(Cn1), and to obtain an NADH-preferring acetoacetyl-CoA reductase derived from this protein, some engineered enzymes were expressed, purified and kinetically characterized, together with the parental AAR(Cn1). One of these engineered enzymes, Chimera 5, experimentally showed a selectivity ratio ((k(cat)/K-M)(NADH)/(k(cat)/K-M)(NADPH)) approximate to 18, which is 160 times higher than the selectivity ratio experimentally observed in the parental AAR(Cn1). A thermodynamic-kinetic approach was employed to estimate the cofactor preference and flux capacity of Chimera 5 under physiological conditions. According to this approach, Chimera 5 could prefer NADH over NADPH between 25 and 150 times. Being a derivative of AAR(Cn1), Chimera 5 should be readily functional in Escherichia coli and C. necator. Moreover, with the expected expression level, its activity should be enough to sustain PHB accumulation fluxes similar to the fluxes previously observed in these biotechnologically relevant cell factories. (AU)

• Processo FAPESP: 17/50249-6 - Uma nova estratégia de produção de poliidroxialcanoatos (PHA) por anaerobiose
• Beneficiário: Jonas Contiero
• Modalidade de apoio: Auxílio à Pesquisa - Temático