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. 2025 Jan 7;10(2):410–420. doi: 10.1016/j.synbio.2025.01.001

Fig. 6.

Fig. 6

Quantification of intracellular NAD(H/+) levels and transcriptome analysis of the related genes. (a) Quantification of the intracellular NADH, NAD+, and total NAD(H/+) levels of the strains MY and cR-1 in MFCs. (b) Relative expression levels of NADH dehydrogenase-related genes were assessed in the strains MY and cR-1. nuoA: gene coding NADH-quinone oxidoreductase subunit A; nuoB: gene coding NADH-quinone oxidoreductase subunit B; nuoCD: gene coding NADH-quinone oxidoreductase subunit C/D; nuoE: gene coding NADH-quinone oxidoreductase subunit E; nuoF: gene coding NADH-quinone oxidoreductase subunit F; nuoG: gene coding NADH-quinone oxidoreductase subunit G; nuoH: gene coding NADH-quinone oxidoreductase subunit H; nuoI: gene coding NADH-quinone oxidoreductase subunit I; nuoJ: gene coding NADH-quinone oxidoreductase subunit J; nuoK: gene coding NADH-quinone oxidoreductase subunitK; nuoL: gene coding NADH-quinone oxidoreductase subunit L; nuoM: gene coding NADH-quinone oxidoreductase subunit M; nuoN: gene coding NADH-quinone oxidoreductase subunit N. The expression level of the aforementioned genes in strain MY is designated as 1, while the relative expression levels of the above genes in the strains MY and cR-1 were recorded as error bars denote standard error.